{"id":4291,"date":"2018-12-16T09:03:24","date_gmt":"2018-12-16T17:03:24","guid":{"rendered":"http:\/\/www.wou.edu\/chemistry\/?page_id=4291"},"modified":"2019-01-27T19:04:33","modified_gmt":"2019-01-28T03:04:33","slug":"ch103-chapter-5-covalent-bonds-organic-functional-groups-and-biological-molecules","status":"publish","type":"page","link":"https:\/\/wou.edu\/chemistry\/courses\/online-chemistry-textbooks\/ch103-allied-health-chemistry\/ch103-chapter-5-covalent-bonds-organic-functional-groups-and-biological-molecules\/","title":{"rendered":"CH103 &#8211; Chapter 5: Covalent Bonds and Introduction to Organic Molecules"},"content":{"rendered":"<h2 id=\"CH103top5\"><strong>Chapter 5: Covalent Bonds<\/strong><span><strong> and Introduction to Organic Molecules<br \/>\n<\/strong><\/span><\/h2>\n<p><span style=\"color: #000000\">This text is published under creative commons licensing, for referencing and adaptation, please click <\/span><span style=\"color: #ff0000\"><a href=\"https:\/\/wou.edu\/chemistry\/courses\/online-chemistry-textbooks\/ch103-allied-health-chemistry\/\" style=\"color: #ff0000\"><strong><em>here. <\/em><\/strong><\/a><\/span><\/p>\n<h3><a href=\"#ch150-4.1\"><span><strong>\u00a05.1<\/strong><strong> Introduction to Covalent Molecules and Compounds<\/strong><\/span><\/a><\/h3>\n<h4 id=\"bonds\"><a href=\"#4.1bonds\"><span><strong>How to Recognize Covalent Bonds<\/strong><\/span><\/a><\/h4>\n<h3 id=\"sharing\"><a href=\"#4.2sharing\"><span><strong>5.2 Electron Sharing<\/strong><\/span><\/a><\/h3>\n<h4><a href=\"#ch150-single1\"><strong><span>Single Covalent Bonds Between the Same Atoms<\/span><\/strong><\/a><\/h4>\n<h4 id=\"different\"><span><a href=\"#4.2different\"><strong>Single Covalent Bonds Between Different Atoms<\/strong><\/a><\/span><\/h4>\n<h4 id=\"multiple\"><a href=\"#4.2multiple\"><strong><span>Multiple Covalent Bonds<\/span><\/strong><\/a><\/h4>\n<h4><a href=\"#4.2coordinate\"><span><strong>Coordinate Covalent Bonds<\/strong><\/span><\/a><\/h4>\n<h3><a href=\"#ch150-4.3\"><strong>5.3 Electronegativity and Bond Polarity<\/strong><\/a><\/h3>\n<h3><a href=\"#ch150-4.4\"><strong>5.4 Properties of Molecular Compounds<\/strong><\/a><\/h3>\n<h3><a href=\"#ch150-4.5\"><span><strong>5.5 Naming Binary Molecular Compounds<\/strong><\/span><\/a><\/h3>\n<h3><a href=\"#intermolecular\"><span style=\"color: #d60606\"><strong>5.6 Intermolecular Forces<\/strong><\/span><\/a><\/h3>\n<h3><a href=\"#drawing\"><strong>5.7 Recognizing and Drawing Organic Molecules<\/strong><\/a><\/h3>\n<h3 id=\"chirality\"><a href=\"#chirality\"><strong><span>5.8 Stereoisomers, Enantiomers, and Chirality<\/span><\/strong><\/a><\/h3>\n<h3 id=\"protein\"><a href=\"#protein\"><span><strong>5.9 The Importance of Chirality in Protein Interactions<\/strong><\/span><\/a><\/h3>\n<h3 id=\"recog\"><a href=\"#recog\"><span><strong>5.10 Common Organic Functional Groups<\/strong><\/span><\/a><\/h3>\n<h3><a href=\"#ch150-4.6\"><span><strong>5.11 Chapter Summary<\/strong><\/span><\/a><\/h3>\n<h3><a href=\"#ch150-4.7\"><span><strong>5.12 References<\/strong><\/span><\/a><\/h3>\n<hr \/>\n<h2><span><strong>Chapter 5 &#8211; <\/strong><\/span><strong>Covalent Bonds<\/strong><span><strong> and Introduction to Organic Molecules<\/strong><\/span><span><strong><\/strong><\/span><\/h2>\n<p><span style=\"color: #000000\">Chemical bonds are generally divided into two fundamentally different types: ionic and covalent. In reality, however, the bonds in most substances are neither purely ionic nor purely covalent, but lie on a spectrum between these extremes. Although purely ionic and purely covalent bonds represent extreme cases that are seldom encountered in any\u00a0but very simple substances, a brief discussion of these two extremes helps explain why substances with different kinds of chemical bonds have very different properties. Ionic compounds consist of positively and negatively charged ions held together by strong electrostatic forces, whereas covalent compounds generally consist of molecules, which are groups of atoms in which one or more pairs of electrons are shared between bonded atoms. In a covalent bond, atoms are held together by the electrostatic attraction between the positively charged nuclei of the bonded atoms and the negatively charged electrons they share. This chapter will focus on the properties of covalent compounds.<\/span><\/p>\n<h3 id=\"ch150-4.1\"><span><strong>\u00a05.1<\/strong><strong> Introduction to Covalent Molecules and Compounds<br \/>\n<\/strong><\/span><\/h3>\n<p><span style=\"color: #000000\">Just as an atom is the simplest unit that has the fundamental chemical properties of an element, <strong><em>a molecule<\/em> <\/strong>is the simplest unit that has the fundamental chemical properties of a covalent compound. Thus, the term <strong><em>molecular compound<\/em><\/strong> is used to describe elements that are covalently bonded and to distinguish the compounds from ionic compounds. Some pure elements exist as covalent molecules. Hydrogen, nitrogen, oxygen, and the halogens occur naturally as the diatomic (\u201ctwo atoms\u201d) molecules H<sub>2<\/sub>, N<sub>2<\/sub>, O<sub>2<\/sub>, F<sub>2<\/sub>, Cl<sub>2<\/sub>, Br<sub>2<\/sub>, and I<sub>2<\/sub> (part (a) in Figure <span class=\"MathJax\" id=\"MathJax-Element-1-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-1\"><span class=\"mrow\" id=\"MathJax-Span-2\"><span class=\"texatom\" id=\"MathJax-Span-3\"><span class=\"mrow\" id=\"MathJax-Span-4\"><span class=\"mn\" id=\"MathJax-Span-5\">4.1<\/span><span class=\"mn\" id=\"MathJax-Span-6\"><\/span><\/span><\/span><\/span><\/span><\/span>). Similarly, a few pure elements exist as\u00a0polyatomic (\u201cmany atoms\u201d) molecules, such as elemental phosphorus and sulfur, which occur as P<sub>4<\/sub> and S<sub>8<\/sub> (part (b) in Figure 5<span class=\"MathJax\" id=\"MathJax-Element-2-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-7\"><span class=\"mrow\" id=\"MathJax-Span-8\"><span class=\"texatom\" id=\"MathJax-Span-9\"><span class=\"mrow\" id=\"MathJax-Span-10\"><span class=\"mn\" id=\"MathJax-Span-11\">.1<\/span><span class=\"mn\" id=\"MathJax-Span-12\"><\/span><\/span><\/span><\/span><\/span><\/span>).<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/molecules.jpg\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/molecules-1024x453.jpg\" alt=\"\" class=\"alignnone wp-image-3263\" width=\"687\" height=\"304\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/molecules-1024x453.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/molecules-300x133.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/molecules-768x340.jpg 768w\" sizes=\"(max-width: 687px) 100vw, 687px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.1 Elements That Exist as Covalent Molecules.<\/strong> (a) Several elements naturally exist as diatomic molecules, in which two atoms (E) are joined by one or more covalent bonds to form a molecule with the general formula E2. (b) A few elements naturally exist as polyatomic molecules, which contain more than two atoms. For example, phosphorus exists as P4 tetrahedra\u2014regular polyhedra with four triangular sides\u2014with a phosphorus atom at each vertex. Elemental sulfur consists of a puckered ring of eight sulfur atoms connected by single bonds. Selenium is not shown due to the complexity of its structure.<\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">Each covalent compound is represented by a molecular formula, which gives the atomic symbol for each component element, in a prescribed order, accompanied by a subscript indicating the number of atoms of that element in the molecule. The subscript is written only if the number of atoms is greater than 1. For example, water, with two hydrogen atoms and one oxygen atom per molecule, is written as <span class=\"MathJax\" id=\"MathJax-Element-3-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-13\"><span class=\"mrow\" id=\"MathJax-Span-14\"><span class=\"msubsup\" id=\"MathJax-Span-15\"><span class=\"mi\" id=\"MathJax-Span-16\">H<\/span><sub><span class=\"mn\" id=\"MathJax-Span-17\">2<\/span><\/sub><\/span><span class=\"mi\" id=\"MathJax-Span-18\">O. <\/span><\/span><\/span><\/span>Similarly, carbon dioxide, which contains one carbon atom and two oxygen atoms in each molecule, is written as <span class=\"MathJax\" id=\"MathJax-Element-4-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-19\"><span class=\"mrow\" id=\"MathJax-Span-20\"><span class=\"mi\" id=\"MathJax-Span-21\">C<\/span><span class=\"msubsup\" id=\"MathJax-Span-22\"><span class=\"mi\" id=\"MathJax-Span-23\">O<\/span><sub><span class=\"mn\" id=\"MathJax-Span-24\">2<\/span><\/sub><\/span><\/span><\/span><\/span>.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen_exception_to_octet.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-1987\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen_exception_to_octet.png\" width=\"760\" height=\"177\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen_exception_to_octet.png 760w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen_exception_to_octet-300x70.png 300w\" sizes=\"(max-width: 760px) 100vw, 760px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Covalent compounds that contain carbon and hydrogen are called <em><strong>organic compounds<\/strong><\/em>. The convention for representing the formulas of organic compounds is to write carbon first, followed by hydrogen and then any other elements in alphabetical order (e.g., CH<sub>4<\/sub>O is methyl alcohol, a fuel). Compounds that consist primarily of elements other than carbon and hydrogen are called <strong><em>inorganic compounds<\/em><\/strong>; they include both covalent and ionic compounds. The convention for writing inorganic compounds, involves listing the component elements beginning with the one farthest to the left in the periodic table, as\u00a0in SO<sub>2<\/sub> or SF<sub>6<\/sub>. Those in the same group are listed beginning with the lower element and working up, as in ClF. By convention, however, when an inorganic compound contains both hydrogen and an element from groups 13\u201315, hydrogen is usually listed last in the formula. Examples are ammonia (NH<sub>3<\/sub>) and silane (SiH<sub>4<\/sub>). Compounds such as water, whose compositions were established long before this convention was adopted, are always written with hydrogen first: Water is always written as H<sub>2<\/sub>O, not OH<sub>2<\/sub>. Typically this distinguishes when hydrogen is participating in a covalent bond rather than an ionic interaction, as seen in many of the inorganic acids, such as hydrochloric acid (HCl) and sulfuric acid (H<sub>2<\/sub>SO<sub>4<\/sub>), as described in chapter 4<span class=\"external\"><\/span>.<\/span><\/p>\n<hr \/>\n<h4 id=\"4.1bonds\"><span><strong>How to Recognize Covalent Bonds<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">In Chapter 4, we saw that ionic compounds are composed predominantly of a metal + a nonmetal.\u00a0 Covalent molecules, on the otherhand, are typically composed of two nonmetals or a nonmetal and a metalloid.\u00a0 This is an initial screening method that you can use to categorize compounds into the ionic or the covalent cagetogy.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ionic-vs-covalent-bonds.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ionic-vs-covalent-bonds-1024x470.png\" alt=\"\" class=\"alignnone wp-image-3268\" width=\"691\" height=\"317\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ionic-vs-covalent-bonds-1024x470.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ionic-vs-covalent-bonds-300x138.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ionic-vs-covalent-bonds-768x353.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ionic-vs-covalent-bonds.png 1708w\" sizes=\"(max-width: 691px) 100vw, 691px\" \/><\/a><\/p>\n<p><span><span style=\"color: #000000\"><strong>Figure 5.2 Recognizing Ionic vs Covalent Compounds.<\/strong> Typically compounds that are formed from a combination of a metal with a nonmetal have more ionic bond character whereas compounds formed from two nonmetals or a metalloid and a nonmetal show more covalent character. Although compounds usually lie on a spectrum somewhere between fully ionic and fully covalent character, for naming purposes, this guideline works well.<\/span><br \/>\n<\/span><\/p>\n<h4><a href=\"#CH103top5\"><span style=\"color: #ff0000\"><em><strong>(back to the top)<\/strong><\/em><\/span><\/a><\/h4>\n<hr \/>\n<h3 id=\"4.2sharing\"><span style=\"color: #d60606\"><strong>5.2 Electron Sharing<\/strong><\/span><\/h3>\n<h4><span style=\"color: #d60606\"><strong>Predicting the Correct Number of Bonds<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">Recall that the octet rule helped us determine that carbon has four electrons in its valence shell and would thus, need to create four covalent bonds to reach an octet. Similarly, nitrogen and phosphorus each make three bonds, oxygen\u00a0and sulfur each make two, and\u00a0the halogens only make one bond.\u00a0Hydrogen is an exception to the octet rule as it is the smallest element and its valence shell is filled with two electrons.\u00a0 Thus, hydrogen can only form one bond with another atom. Sulfur and phosphorus can also have bonding patterns that are exceptions to the octet rule.\u00a0 They both can have expanded orbital bonding with phosphorus also routinely forming five covalent bonds, and sulfur being capable of forming either four or six covalent bonds. Table 5.1 provides a graphic representation of these patterns. When you are drawing organic molecules, it is important to pay attention to the bonding rules so that all atoms reach their preferred bonding states.<\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Table 5.1:\u00a0 Covalent Bonding Patterns of Atoms Commonly Atoms<\/strong><\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonding_table_for_organic-2.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2013\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonding_table_for_organic-2.png\" width=\"684\" height=\"548\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonding_table_for_organic-2.png 748w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonding_table_for_organic-2-300x240.png 300w\" sizes=\"(max-width: 684px) 100vw, 684px\" \/><\/a><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonding_table_for_organic.png\"><\/a><\/p>\n<p><span style=\"color: #000000\">*Note: Hydrogen doesn&#8217;t really follow the octet rule as its valence shell is full with 2 <em>e<sup>&#8211;<\/sup><\/em><\/span><\/p>\n<h4 id=\"ch150-single1\"><strong><span>Single Covalent Bonds Between the Same Atoms<\/span><br \/>\n<\/strong><\/h4>\n<p><span style=\"color: #000000\">Chapter 4 described how electrons can be transferred from one atom to another so that both atoms have an energy-stable outer electron shell following the <em><strong>octet rule<\/strong><\/em>. However, there is another way an atom can achieve a full valence shell: atoms can share electrons to reach the octet state (or the duet state in the case of hydrogen).<\/span><\/p>\n<p><span style=\"color: #000000\">This concept can be illustrated by using two hydrogen atoms, each of which has a single electron in its valence shell. (For small atoms such as hydrogen atoms, the valence shell will be the first shell, which holds only two electrons.) We can represent the two individual hydrogen atoms as follows:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-atoms.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1702\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-atoms-1024x576.jpg\" width=\"696\" height=\"392\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-atoms-1024x576.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-atoms-300x169.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-atoms-768x432.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-atoms.jpg 1200w\" sizes=\"(max-width: 696px) 100vw, 696px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">In this situation neither hydrogen can reach the preferred duet state.\u00a0 In contrast, when two hydrogen atoms get close enough together to share their electrons, they can be represented as follows:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonded-hydrogens.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1687\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonded-hydrogens-1024x576.jpg\" width=\"696\" height=\"392\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonded-hydrogens-1024x576.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonded-hydrogens-300x169.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonded-hydrogens-768x432.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonded-hydrogens.jpg 1200w\" sizes=\"(max-width: 696px) 100vw, 696px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">By sharing their valence electrons, both hydrogen atoms now have two electrons in their respective valence shells. Because each valence shell is now filled, this arrangement is more stable than when the two atoms are separate. In this configuration, each hydrogen has an electron configuration equivalent to that of the noble gas, helium. The sharing of electrons between atoms is called a<strong><em> covalent bond<\/em><\/strong>, and the two electrons that join atoms in a covalent bond are called a <strong><em>bonding pair of electrons<\/em><\/strong>. A discrete group of atoms connected by covalent bonds is called a<strong><em> molecule<\/em><\/strong>\u2014the smallest part of a compound that retains the chemical identity of that compound. For example, one molecule of water would contain two hydrogen atoms and one oxygen atom (H<sub>2<\/sub>O).<\/span><\/p>\n<p><span style=\"color: #000000\">Chemists frequently use Lewis electron dot diagrams to represent covalent bonding in molecular substances. For example, the Lewis diagrams of two separate hydrogen atoms are as follows:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1716\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-1024x46.jpg\" width=\"691\" height=\"31\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-1024x46.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-300x14.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-768x35.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen.jpg 1500w\" sizes=\"(max-width: 691px) 100vw, 691px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">The Lewis diagram of two hydrogen atoms sharing electrons looks like this:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1804\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-1-1024x52.jpg\" width=\"689\" height=\"35\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-1-1024x52.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-1-300x15.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-1-768x39.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-1.jpg 1500w\" sizes=\"(max-width: 689px) 100vw, 689px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">This depiction of molecules is simplified further by using a dash to represent a covalent bond. The hydrogen molecule is then represented as follows:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-dash-1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1803\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-dash-1-1024x48.jpg\" width=\"678\" height=\"32\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-dash-1-1024x48.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-dash-1-300x14.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-dash-1-768x36.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-bonded-dash-1.jpg 1500w\" sizes=\"(max-width: 678px) 100vw, 678px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Remember that the dash, also referred to as a single bond, represents a pair of bonding electrons.<\/span><\/p>\n<p><span style=\"color: #000000\">The bond in a hydrogen molecule, measured as the distance between the two nuclei, is about 7.4 \u00d7 10<sup>\u221211<\/sup> m, or 74 picometers (pm; 1 pm = 1 \u00d7 10<sup>\u221212<\/sup> m). This particular bond length represents a balance between several forces:\u00a0 (1) the attractions between oppositely charged electrons and nuclei, (2) the repulsion between two negatively charged electrons, and (3) the repulsion between two positively charged nuclei. If the nuclei were closer together, they would repel each other more strongly; if the nuclei were farther apart, there would be less attraction between the positive and negative particles.<\/span><\/p>\n<p><span style=\"color: #000000\">Fluorine is another element whose atoms bond together in pairs to form diatomic (two-atom) molecules. Two separate fluorine atoms have the following electron dot diagrams:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1806\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-1-1024x83.jpg\" width=\"687\" height=\"56\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-1-1024x83.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-1-300x24.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-1-768x62.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-1.jpg 1500w\" sizes=\"(max-width: 687px) 100vw, 687px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Each fluorine atom contributes one valence electron, making a single bond and giving each atom a complete valence shell, which fulfills the octet rule:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1807\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-1-1024x91.jpg\" width=\"689\" height=\"61\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-1-1024x91.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-1-300x27.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-1-768x68.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-1.jpg 1500w\" sizes=\"(max-width: 689px) 100vw, 689px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">The circles show that each fluorine atom has eight electrons around it. As with hydrogen, we can represent the fluorine molecule with a dash in place of the bonding electrons:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-dash.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1708\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-dash-1024x75.jpg\" width=\"697\" height=\"51\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-dash-1024x75.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-dash-300x22.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-dash-768x56.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-fluorine-bonded-dash.jpg 1500w\" sizes=\"(max-width: 697px) 100vw, 697px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Each fluorine atom has six electrons, or three pairs of electrons, that are not participating in the covalent bond. Rather than being shared, they are considered to belong to a single atom. These are called <strong><em>nonbonding pairs (or lone pairs)<\/em><\/strong> of electrons.<\/span><\/p>\n<h4><a href=\"#CH103top5\"><span style=\"color: #ff0000\"><em><strong>(back to the top)<\/strong><\/em><\/span><\/a><\/h4>\n<hr \/>\n<h4 id=\"4.2different\"><strong>Single Covalent Bonds Between Different Atoms<\/strong><\/h4>\n<p><span style=\"color: #000000\">Now that we have looked at electron sharing between atoms of the same element, let us look at covalent bond formation between atoms of different elements. Consider a molecule composed of one hydrogen atom and one fluorine atom:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-and-fluorine-1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1809\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-and-fluorine-1-1024x81.jpg\" width=\"696\" height=\"55\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-and-fluorine-1-1024x81.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-and-fluorine-1-300x24.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-and-fluorine-1-768x60.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-and-fluorine-1.jpg 1500w\" sizes=\"(max-width: 696px) 100vw, 696px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Each atom needs one additional electron to complete its valence shell. By each contributing one electron, they make the following molecule:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-fluorine-bond-and-dash.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1715\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-fluorine-bond-and-dash-1024x87.jpg\" width=\"694\" height=\"59\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-fluorine-bond-and-dash-1024x87.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-fluorine-bond-and-dash-300x25.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-fluorine-bond-and-dash-768x65.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-hydrogen-fluorine-bond-and-dash.jpg 1500w\" sizes=\"(max-width: 694px) 100vw, 694px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">In this molecule, the hydrogen atom does not have nonbonding electrons, while the fluorine atom has six nonbonding electrons (three lone electron pairs). The circles show how the valence electron shells are filled for both atoms (recall that hydrogen is filled with two electrons).<\/span><\/p>\n<p><span style=\"color: #000000\">Larger molecules are constructed in a similar fashion, with some atoms participating in more than one covalent bond. For example, water, with two hydrogen atoms and one oxygen atom, and methane (CH<sub>4<\/sub>), with one carbon atom and four hydrogen atoms, can be represented as follows:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-water-and-methane-1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1815\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-water-and-methane-1-1024x142.jpg\" width=\"695\" height=\"96\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-water-and-methane-1-1024x142.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-water-and-methane-1-300x42.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-water-and-methane-1-768x106.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-water-and-methane-1.jpg 1500w\" sizes=\"(max-width: 695px) 100vw, 695px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Atoms typically form a characteristic number of covalent bonds in compounds. Figure 5.3 shows valence electron configurations of each element family (or column).<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/valence-electrons-1.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/valence-electrons-1-1024x849.png\" alt=\"\" class=\"alignnone wp-image-3269\" width=\"690\" height=\"572\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/valence-electrons-1-1024x849.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/valence-electrons-1-300x249.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/valence-electrons-1-768x637.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/valence-electrons-1.png 1562w\" sizes=\"(max-width: 690px) 100vw, 690px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Fig 5.3 Periodic Table with Lewis Structures.<\/strong>\u00a0 Each family shows a representative lewis structure for that group of elements.\u00a0 For the nonmetals (Families 4A, 5A, 6A, and 7A) they can accept a complementary number of shared bonds to reach the octet state. Family 4A can share 4 covalent bonds (4 + 4 = 8), whereas Families 5A, 6A, and 7A can share 3, 2, and 1 covalent bond(s), respectively, to achieve the octet state. Exceptions to the octet rule do exist. For example, hydrogen can be considered to be in Group 1 or Group 7A because it has properties similar to both groups. Hydrogen can participate in either ionic or covalent bonding. When participating in covalent bonding, hydrogen only needs two electrons to have a full valence shell. As it has one electron to start with, it can only make one covalent bond. Similarly, boron has 3 electrons in its outer shell.\u00a0 This nonmetal typically forms 3 covalent bonds, having a maximum of 6 electrons in its outer shell.\u00a0 Thus, boron can never reach the octet state. Other atoms can have expanded orbitals and accept additional covalent bonds. Two of these that are important for living systems are sulfur and phosphorus. By the octet rule, sulfur can make 2 covalent bonds and phosphorus 3 covalent bonds. Sulfur can also have expanded orbitals to accept 4 or 6 covalent bonds, and phosphorus can expand to 5 covalent bonds.<\/span><\/p>\n<hr \/>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/concept_review-2.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1817\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/concept_review-2.png\" width=\"671\" height=\"730\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/concept_review-2.png 664w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/concept_review-2-276x300.png 276w\" sizes=\"(max-width: 671px) 100vw, 671px\" \/><\/a><\/p>\n<h4><a href=\"#CH103top5\"><strong><em><span style=\"color: #ff0000\">(back to the top)<\/span><\/em><\/strong><\/a><\/h4>\n<hr \/>\n<h4 id=\"4.2multiple\"><strong><span>Multiple Covalent Bonds<\/span><\/strong><\/h4>\n<p><span style=\"color: #000000\">In many molecules, the octet rule would not be satisfied if each pair of bonded atoms shares only two electrons. Consider carbon dioxide (CO<sub>2<\/sub>). If each oxygen atom shares one electron with the carbon atom, we get the following:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-the-wrong-way.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1723\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-the-wrong-way-1024x265.jpg\" width=\"692\" height=\"179\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-the-wrong-way-1024x265.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-the-wrong-way-300x78.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-the-wrong-way-768x199.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-the-wrong-way.jpg 1500w\" sizes=\"(max-width: 692px) 100vw, 692px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">This does not give either the carbon or oxygen atoms a complete octet; The carbon atom only has six electrons in its valence shell and each oxygen atom only has seven electrons in its valence shell. Thus, none of the atoms can reach the octet state in the current configuration. As written, this would be an unstable molecular conformation.<\/span><\/p>\n<p><span style=\"color: #000000\">Sometimes more than one pair of electrons must be shared between two atoms for both atoms to have an octet. In carbon dioxide, a second electron from each oxygen atom is also shared with the central carbon atom, and the carbon atom shares one more electron with each oxygen atom:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-correct.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1722\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-correct-1024x225.jpg\" width=\"692\" height=\"152\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-correct-1024x225.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-correct-300x66.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-correct-768x169.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-structure-carbon-dioxide-correct.jpg 1499w\" sizes=\"(max-width: 692px) 100vw, 692px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">In this arrangement, the carbon atom shares four electrons (two pairs) with the oxygen atom on the left and four electrons with the oxygen atom on the right. There are now eight electrons around each atom. Two pairs of electrons shared between two atoms make a double bond between the atoms, which is represented by a double dash:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/carbon-dioxide-lewis-with-dash.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1688\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/carbon-dioxide-lewis-with-dash-1024x76.jpg\" width=\"699\" height=\"52\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/carbon-dioxide-lewis-with-dash-1024x76.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/carbon-dioxide-lewis-with-dash-300x22.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/carbon-dioxide-lewis-with-dash-768x57.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/carbon-dioxide-lewis-with-dash.jpg 1500w\" sizes=\"(max-width: 699px) 100vw, 699px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Some molecules contain triple bonds, covalent bonds in which three pairs of electrons are shared by two atoms. A simple compound that has a triple bond is acetylene (C<sub>2<\/sub>H<sub>2<\/sub>), whose Lewis diagram is as follows:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-methyne-1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1812\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-methyne-1-1024x81.jpg\" width=\"695\" height=\"55\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-methyne-1-1024x81.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-methyne-1-300x24.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-methyne-1-768x60.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/lewis-methyne-1.jpg 1500w\" sizes=\"(max-width: 695px) 100vw, 695px\" \/><\/a><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/concept_review_ii.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1818\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/concept_review_ii.png\" width=\"694\" height=\"785\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/concept_review_ii.png 661w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/concept_review_ii-265x300.png 265w\" sizes=\"(max-width: 694px) 100vw, 694px\" \/><\/a><\/p>\n<hr \/>\n<h4 id=\"4.2coordinate\"><strong><span>Coordinate Covalent Bonds<\/span><\/strong><\/h4>\n<p><span><span style=\"color: #000000\">A coordinate bond (also called a dative covalent bond) is a covalent bond (a shared pair of electrons) in which <strong>both <\/strong>electrons come from the same atom. A covalent bond is formed by two atoms sharing a pair of electrons. The atoms are held together because the electron pair is attracted by both of the nuclei. In the formation of a simple or ordinary covalent bond, each atom supplies one electron to the bond &#8211; but that does not have to be the case. In the case of a coordinate covalent bond, one atom supplies both of the electrons and the other atom does not supply any of the electrons. The following reaction between ammonia and hydrochloric acid demonstrates the formation of a coordinate covalent bond between ammonia and a hydrogren ion (proton).<\/span><br \/>\n<\/span><\/p>\n<div class=\"mt-section\" id=\"section_1\">\n<h5 class=\"editable\"><span style=\"color: #000000\"><em>The reaction between ammonia and hydrochloric acid<br \/>\n<\/em><\/span><\/h5>\n<p><span style=\"color: #000000\">If these colorless gases are allowed to mix, a thick white smoke of solid ammonium chloride is formed.<\/span><\/p>\n<div class=\"mt-video-widget\">\n<div class=\"editable\">\n<div class=\"mt-video-widget\">\n<div>\n<div style=\"width: 480px;\" class=\"wp-video\"><video class=\"wp-video-shortcode\" id=\"video-4291-1\" width=\"480\" height=\"360\" preload=\"metadata\" controls=\"controls\"><source type=\"video\/mp4\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/Gas-Phase-Acid-Base-Reaction-Between-Ammonia-and-Hydrochloric-Acid.mp4?_=1\" \/><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/Gas-Phase-Acid-Base-Reaction-Between-Ammonia-and-Hydrochloric-Acid.mp4\">https:\/\/wou.edu\/chemistry\/files\/2017\/04\/Gas-Phase-Acid-Base-Reaction-Between-Ammonia-and-Hydrochloric-Acid.mp4<\/a><\/video><\/div>\n<p><span style=\"color: #000000\">Video provided by<\/span> <a href=\"https:\/\/www.youtube.com\/user\/NCSSMDistanceEd\/featured\">North Carolina School of Science and Mathematics<\/a><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><span style=\"color: #000000\">The overall reaction is<\/span><\/p>\n<div class=\"MathJax_Display\"><span class=\"MathJax\" id=\"MathJax-Element-1-Frame\" role=\"presentation\" style=\"color: #000000\"><span class=\"math\" id=\"MathJax-Span-1\"><strong><span class=\"mrow\" id=\"MathJax-Span-2\"><span class=\"mi\" id=\"MathJax-Span-3\">N<\/span><span class=\"msubsup\" id=\"MathJax-Span-4\"><span class=\"mi\" id=\"MathJax-Span-5\">H<\/span><span class=\"texatom\" id=\"MathJax-Span-6\"><span class=\"mrow\" id=\"MathJax-Span-7\"><sub><span class=\"mn\" id=\"MathJax-Span-8\">3<\/span><\/sub><span class=\"mo\" id=\"MathJax-Span-9\">(<\/span><span class=\"mi\" id=\"MathJax-Span-10\">g<\/span><span class=\"mo\" id=\"MathJax-Span-11\">) <\/span><\/span><\/span><\/span><span class=\"mo\" id=\"MathJax-Span-12\">+ <\/span><span class=\"mi\" id=\"MathJax-Span-13\">H<\/span><span class=\"mi\" id=\"MathJax-Span-14\">C<\/span><span class=\"msubsup\" id=\"MathJax-Span-15\"><span class=\"mi\" id=\"MathJax-Span-16\">l<\/span><span class=\"texatom\" id=\"MathJax-Span-17\"><span class=\"mrow\" id=\"MathJax-Span-18\"><span class=\"mo\" id=\"MathJax-Span-19\">(<\/span><span class=\"mi\" id=\"MathJax-Span-20\">g<\/span><span class=\"mo\" id=\"MathJax-Span-21\">) <\/span><\/span><\/span><\/span><span class=\"mo\" id=\"MathJax-Span-22\">\u2192 <\/span><span class=\"mi\" id=\"MathJax-Span-23\">N<\/span><span class=\"msubsup\" id=\"MathJax-Span-24\"><span class=\"mi\" id=\"MathJax-Span-25\">H<\/span><sub><span class=\"mn\" id=\"MathJax-Span-26\">4<\/span><\/sub><\/span><span class=\"mi\" id=\"MathJax-Span-27\">C<\/span><span class=\"msubsup\" id=\"MathJax-Span-28\"><span class=\"mi\" id=\"MathJax-Span-29\">l<\/span><span class=\"texatom\" id=\"MathJax-Span-30\"><span class=\"mrow\" id=\"MathJax-Span-31\"><span class=\"mo\" id=\"MathJax-Span-32\">(<\/span><span class=\"mi\" id=\"MathJax-Span-33\">s<\/span><span class=\"mo\" id=\"MathJax-Span-34\">)<\/span><\/span><\/span><\/span><\/span><\/strong><\/span><\/span><\/div>\n<div class=\"MathJax_Display\"><\/div>\n<\/div>\n<p><span><span style=\"color: #000000\">Ammonium ions, NH<sub>4<\/sub><sup>+<\/sup>, are formed by the transfer of a hydrogen ion (a proton) from the hydrochloric acid molecule to the lone pair of electrons on the ammonia molecule. To visualize this reaction, we can use electron dot configurations to observe the electron movement during the reaction.\u00a0 First recall the valence electron states for all of the atoms involved in the reaction:<\/span><br \/>\n<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/Valence-Shell-Status.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/Valence-Shell-Status.png\" alt=\"\" class=\"alignnone wp-image-3275\" width=\"555\" height=\"166\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/Valence-Shell-Status.png 666w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/Valence-Shell-Status-300x90.png 300w\" sizes=\"(max-width: 555px) 100vw, 555px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">On the left side of the equation (to the left of the arrow) are the reactants of the reaction (ammonia and hydrochloric acid).\u00a0 On the right side of the reaction (to the right of the arrow) is the product of the reaction, the ionic compound &#8211; ammonium chloride.\u00a0 The diagram below shows the electron and proton movement during the reaction.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ammonium-chloride.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ammonium-chloride-1024x345.png\" alt=\"\" class=\"alignnone wp-image-3276\" width=\"695\" height=\"234\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ammonium-chloride-1024x345.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ammonium-chloride-300x101.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ammonium-chloride-768x259.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/ammonium-chloride.png 1221w\" sizes=\"(max-width: 695px) 100vw, 695px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.4 Formation of Ammonium Chloride.<\/strong> When the ammonium ion, NH<sub>4<\/sub><sup>+<\/sup>, is formed, the fourth hydrogen (shown in red) is attached by a coordinate covalent bond, because only the hydrogen&#8217;s nucleus is transferred from the chlorine to the nitrogen. The hydrogen&#8217;s electron is left behind on the chlorine to form a negative chloride ion. Once the ammonium ion has been formed it is impossible to tell any difference between the coordinate covalent and the ordinary covalent bonds, all of the hydrogens are equivalent in the molecule and the extra positive charge is distributed throughout the molecule. Although the electrons are shown differently in the diagram, there is no difference between them in reality. In simple diagrams, a coordinate bond is shown by a curved arrow. The arrow points from the atom donating the lone pair to the atom accepting it.<\/span><\/p>\n<h4><a href=\"#CH103top5\"><strong><em><span style=\"color: #ff0000\">(back to the top)<\/span><\/em><\/strong><\/a><\/h4>\n<hr \/>\n<h3 id=\"ch150-4.3\"><strong>5.3 Electronegativity and Bond Polarity<\/strong><\/h3>\n<p><span style=\"color: #000000\">Although we defined covalent bonding as electron sharing, the electrons in a covalent bond are not always shared equally by the two bonded atoms. Unless the bond connects two atoms of the same element, there will always be one atom that attracts the electrons in the bond more strongly than the other atom does, as shown in Figure 5.5. When such an imbalance occurs, there is a resulting buildup of some negative charge (called a partial negative charge and designated \u03b4\u2212) on one side of the bond and some positive charge (designated \u03b4+) on the other side of the bond. A covalent bond that has an unequal sharing of electrons, as in part (b) of Figure 5.5, is called a <em><strong>polar covalent bond<\/strong><\/em>. A covalent bond that has an equal sharing of electrons (part (a) of Figure 5.5) is called a <strong><em>nonpolar covalent bond<\/em><\/strong>.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/polar-vs-nonpolar.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1896 aligncenter\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/polar-vs-nonpolar-597x1024.jpg\" width=\"445\" height=\"763\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/polar-vs-nonpolar-597x1024.jpg 597w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/polar-vs-nonpolar-175x300.jpg 175w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/polar-vs-nonpolar-768x1318.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/polar-vs-nonpolar.jpg 940w\" sizes=\"(max-width: 445px) 100vw, 445px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.5 Polar versus Nonpolar Covalent Bonds.<\/strong> (a) The electrons in the covalent bond are equally shared by both hydrogen atoms. This is a nonpolar covalent bond. (b) The fluorine atom attracts the electrons in the bond more than the hydrogen atom does, leading to an imbalance in the electron distribution. This is a polar covalent bond.<\/span><\/p>\n<hr \/>\n<h4><span style=\"color: #000000\"><strong>Video Tutorial on Nonpolar Covalent Bonds<\/strong><\/span><\/h4>\n<div style=\"width: 824px;\" class=\"wp-video\"><video class=\"wp-video-shortcode\" id=\"video-4291-2\" width=\"824\" height=\"604\" preload=\"metadata\" controls=\"controls\"><source type=\"video\/mp4\" src=\"https:\/\/wou.edu\/chemistry\/files\/2019\/01\/nonpolar-covalent-bond.mp4?_=2\" \/><a href=\"https:\/\/wou.edu\/chemistry\/files\/2019\/01\/nonpolar-covalent-bond.mp4\">https:\/\/wou.edu\/chemistry\/files\/2019\/01\/nonpolar-covalent-bond.mp4<\/a><\/video><\/div>\n<h4><strong><span style=\"color: #000000\">Video Tutorial On Polar Covalent Bonds<\/span><\/strong><\/h4>\n<div style=\"width: 824px;\" class=\"wp-video\"><video class=\"wp-video-shortcode\" id=\"video-4291-3\" width=\"824\" height=\"604\" preload=\"metadata\" controls=\"controls\"><source type=\"video\/mp4\" src=\"https:\/\/wou.edu\/chemistry\/files\/2019\/01\/Polar-covalent-bonds.mp4?_=3\" \/><a href=\"https:\/\/wou.edu\/chemistry\/files\/2019\/01\/Polar-covalent-bonds.mp4\">https:\/\/wou.edu\/chemistry\/files\/2019\/01\/Polar-covalent-bonds.mp4<\/a><\/video><\/div>\n<hr \/>\n<p><span style=\"color: #000000\">Any covalent bond between atoms of different elements is a polar bond, but the degree of polarity varies widely. Some bonds between different elements are only minimally polar, while others are strongly polar. Ionic bonds can be considered the ultimate in polarity, with electrons being transferred completely rather than shared. To judge the relative polarity of a covalent bond, chemists use <em><strong>electronegativity<\/strong><\/em>, which is a relative measure of how strongly an atom attracts electrons when it forms a covalent bond.<\/span><\/p>\n<p><span style=\"color: #000000\">There are various numerical scales for rating electronegativity. Figure 5.6 shows one of the most popular\u2014<em><strong>the Pauling scale<\/strong><\/em>. The polarity of a covalent bond can be judged by determining the difference in the electronegativities\u00a0between the two atoms making the bond. The greater the difference in electronegativities, the greater the imbalance of electron sharing in the bond.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/eletronegativity.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1880\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/eletronegativity-1024x663.jpg\" width=\"686\" height=\"444\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/eletronegativity-1024x663.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/eletronegativity-300x194.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/eletronegativity-768x497.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/eletronegativity.jpg 1538w\" sizes=\"(max-width: 686px) 100vw, 686px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.6 Electronegativities of Various Elements.\u00a0<\/strong>The Pauling Scale for electronegativities has the value for fluorine atoms set at 4.0, the highest value.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Linus_Pauling.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1921\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Linus_Pauling.png\" width=\"686\" height=\"862\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Linus_Pauling.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Linus_Pauling-239x300.png 239w\" sizes=\"(max-width: 686px) 100vw, 686px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Although there are no hard and fast rules, the general rule is\u00a0that\u00a0a difference in electronegativity less than 0.4 indicates\u00a0the bond is nonpolar;\u00a0when the difference is greater than 0.4, the bond is considered polar.\u00a0When the difference in electronegativities is large enough (generally greater than about 1.8), the resulting compound is considered ionic rather than covalent. An electronegativity difference of zero, of course, indicates a nonpolar covalent bond. Examples of electronegativity difference are shown in Figure\u00a0 5.7.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Picture1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1895\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Picture1-1024x392.png\" width=\"682\" height=\"261\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Picture1.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Picture1-300x115.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Picture1-768x294.png 768w\" sizes=\"(max-width: 682px) 100vw, 682px\" \/><\/a><\/p>\n<p><span><span style=\"color: #000000\"><strong>Figure 5.7 Electronegativity Difference Diagram.<\/strong> The diagram above is a guide for discerning what type of bond forms between two different atoms. By taking the difference between the electronegativity values for each of the atoms involved in the bond, the bond type and\u00a0polarity can be predicted. Note that full ionic character is rarely reached, however when metals and nonmetals form bonds, they are named using the rules for ionic bonding.<\/span><br \/>\n<\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">When a molecule\u2019s bonds are polar, the molecule as a whole can display an uneven distribution of charge, depending on how the individual bonds are oriented. For example, the orientation of the two O\u2013H bonds in a water molecule (Figure 5.8) is bent: one end of the molecule has a partial positive charge, and the other end has a partial negative charge. In short, the molecule itself is polar. The polarity of water has an enormous impact on its physical and chemical properties. (For example, the boiling point of water [100\u00b0C] is high for such a small molecule and is due to the fact that polar molecules attract each other strongly.) In contrast, while the two C=O bonds in carbon dioxide are polar, they lie directly opposite each other in the molecule\u00a0and so cancel each other\u2019s effects. Thus, carbon dioxide molecules are nonpolar overall. This lack of polarity influences some of carbon dioxide\u2019s properties. (For example, carbon dioxide becomes a gas at \u221277\u00b0C, almost 200\u00b0 lower than the temperature at which water boils.)<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/molecule-polarity.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2292\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/molecule-polarity.png\" width=\"681\" height=\"222\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/molecule-polarity.png 971w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/molecule-polarity-300x98.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/molecule-polarity-768x250.png 768w\" sizes=\"(max-width: 681px) 100vw, 681px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.8 Physical Properties and Polarity.<\/strong> The physical properties of water (a) and carbon dioxide (b) are affected by their molecular polarities. Note that the arrows in the diagram always point in the direction where the electrons are more strongly attracted. In this diagram, the delta symbol (\u03b4) is used with a (+) or (-) symbol to represent partial positive and partial negative charge distribution in polar covalent bonds. Note that the electrons shared in polar covalent bonds will be attracted to and spend more time around the atom with the higher electronegativity value. When the polarity is equal and directly opposing, as in the case of carbon dioxide (b), the overall molecule will have no overall charge.<\/span><\/p>\n<hr \/>\n<h4><span style=\"color: #000000\"><strong>Tutorial on Electronegativity and Bond Polarity By <span style=\"color: #ff0000\"><em><a href=\"https:\/\/www.youtube.com\/watch?v=PoQjsnQmxok\" style=\"color: #ff0000\">Professor Dave Explains<\/a><\/em><\/span><\/strong><\/span><\/h4>\n<hr \/>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/electronegativity_review.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1927\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/electronegativity_review.png\" width=\"683\" height=\"815\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/electronegativity_review.png 539w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/electronegativity_review-251x300.png 251w\" sizes=\"(max-width: 683px) 100vw, 683px\" \/><\/a><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(BACK TO THE TOP)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h3 id=\"ch150-4.4\"><strong>5.4 Properties of Molecular Compounds<\/strong><\/h3>\n<p><span style=\"color: #000000\">Molecular compounds have many properties that differ from ionic compounds.\u00a0 Some of the generalizations for this group include much lower melting and boiling points when compared with their ionic counterpoints.\u00a0 For example, water (H<sub>2<\/sub>O) has a melting point of 4<sup>o<\/sup>C and a boiling point of 100<sup>o<\/sup>C compared with NaCl that has a melting point of 801<sup>o<\/sup>C and a boiling point of 1,413<sup>o<\/sup>C. This is because the full charges created in ionic bonds have much stronger attractive force than the comparatively weak partial charges created in covalent molecules. thus, ionic compounds tend to form very strong crystalline lattice structures due to the repeating charges of the cation and anion components. Covalent compounds, on the otherhand, do not typically have such well-structured 3-dimensional shapes.\u00a0 Thus they tend to be more brittle and break more easily when in solid form, and many are found in liquid and gas phases. In addition, due to their lack of charges, they tend to be poor electrical and thermal conductors. Many are also insoluble in water due to their nonpolar nature (ie oil and water don&#8217;t mix).<\/span><\/p>\n<p><span style=\"color: #000000\">Table 5.2 shows common differences between covalent and ionic compounds.<\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Table 5.2 Comparison of Ionic and Covalent Compounds<\/strong><\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/covalent_vs_ionic.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/covalent_vs_ionic-1024x707.png\" alt=\"\" class=\"alignnone wp-image-3494\" width=\"697\" height=\"481\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/covalent_vs_ionic-1024x707.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/covalent_vs_ionic-300x207.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/covalent_vs_ionic-768x530.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/covalent_vs_ionic.png 1059w\" sizes=\"(max-width: 697px) 100vw, 697px\" \/><\/a><\/p>\n<h3 id=\"ch150-4.5\"><span><strong>5.5 Naming Binary Molecular Compounds<\/strong><\/span><\/h3>\n<p><span style=\"color: #000000\">Recall that a molecular formula shows the number of atoms of each element that a molecule contains. A molecule of water contains two hydrogen atoms and one oxygen atom, so its formula is <span class=\"MathJax\" id=\"MathJax-Element-5-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-41\"><span class=\"mrow\" id=\"MathJax-Span-42\"><span class=\"msubsup\" id=\"MathJax-Span-43\"><span class=\"mtext\" id=\"MathJax-Span-44\">H<\/span><span class=\"texatom\" id=\"MathJax-Span-45\"><span class=\"mrow\" id=\"MathJax-Span-46\"><span class=\"mspace\" id=\"MathJax-Span-47\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-48\"><span class=\"mrow\" id=\"MathJax-Span-49\"><span class=\"mn\" id=\"MathJax-Span-50\">2<\/span><\/span><\/span><\/sub><\/span><span class=\"mtext\" id=\"MathJax-Span-51\">O<\/span><\/span><\/span><\/span>. A molecule of octane, which is a component of gasoline, contains 8 atoms of carbon and 18 atoms of hydrogen. The molecular formula of octane is <\/span><span class=\"MathJax\" id=\"MathJax-Element-6-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-52\"><span style=\"color: #000000\"><span class=\"mrow\" id=\"MathJax-Span-53\"><span class=\"msubsup\" id=\"MathJax-Span-54\"><span class=\"mtext\" id=\"MathJax-Span-55\">C<\/span><span class=\"texatom\" id=\"MathJax-Span-56\"><span class=\"mrow\" id=\"MathJax-Span-57\"><span class=\"mspace\" id=\"MathJax-Span-58\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-59\"><span class=\"mrow\" id=\"MathJax-Span-60\"><span class=\"mn\" id=\"MathJax-Span-61\">8<\/span><\/span><\/span><\/sub><\/span><span class=\"msubsup\" id=\"MathJax-Span-62\"><span class=\"mtext\" id=\"MathJax-Span-63\">H<\/span><span class=\"texatom\" id=\"MathJax-Span-64\"><span class=\"mrow\" id=\"MathJax-Span-65\"><span class=\"mspace\" id=\"MathJax-Span-66\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-67\"><span class=\"mrow\" id=\"MathJax-Span-68\"><span class=\"mn\" id=\"MathJax-Span-69\">18<\/span><\/span><\/span><\/sub><span class=\"texatom\" id=\"MathJax-Span-67\"><span class=\"mrow\" id=\"MathJax-Span-68\"><span class=\"mn\" id=\"MathJax-Span-69\">. When writing the chemical formula the element that is the least electronegative (the element that is farther left or further down within the same family group) is written first while the more electronegative element is written second. You will be required to know how to name simple binary covalent compounds (compounds composed of two different elements)<\/span><\/span><\/span><\/span><\/span><\/span><span><\/span><\/span><\/span><\/p>\n<p>.<\/p>\n<p><img decoding=\"async\" alt=\"\" class=\"internal default alignleft\" src=\"https:\/\/chem.libretexts.org\/@api\/deki\/files\/78189\/CK12_Screenshot_7-11-2.png?revision=1&amp;size=bestfit&amp;width=113&amp;height=201\" width=\"113px\" height=\"201px\" \/><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5<span class=\"MathJax\" id=\"MathJax-Element-7-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-70\"><span class=\"mrow\" id=\"MathJax-Span-71\"><span class=\"texatom\" id=\"MathJax-Span-72\"><span class=\"mrow\" id=\"MathJax-Span-73\"><span class=\"mn\" id=\"MathJax-Span-74\">.9<\/span><span class=\"mn\" id=\"MathJax-Span-75\"><\/span><\/span><\/span><\/span><\/span><\/span> Nitrogen dioxide <span class=\"MathJax\" id=\"MathJax-Element-8-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-76\"><span class=\"mrow\" id=\"MathJax-Span-77\"><span class=\"mrow\" id=\"MathJax-Span-78\"><span class=\"mo\" id=\"MathJax-Span-79\">(<\/span><span class=\"msubsup\" id=\"MathJax-Span-80\"><span class=\"mtext\" id=\"MathJax-Span-81\">NO<\/span><span class=\"texatom\" id=\"MathJax-Span-82\"><span class=\"mrow\" id=\"MathJax-Span-83\"><span class=\"mspace\" id=\"MathJax-Span-84\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-85\"><span class=\"mrow\" id=\"MathJax-Span-86\"><span class=\"mn\" id=\"MathJax-Span-87\">2<\/span><\/span><\/span><\/sub><\/span><span class=\"mo\" id=\"MathJax-Span-88\">) <\/span><\/span><\/span><\/span><\/span><\/strong>is a reddish-brown toxic gas that is a prominent air pollutant produced by internal combustion engines.<\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">The elements that combine to form binary molecular compounds are both nonmetal atoms or they are a combination of a nonmetal and a metalloid. This contrasts with ionic compounds, which were formed from a metal ion and a nonmetal ion. Therefore, binary molecular compounds are different because ionic charges cannot be used to name them or to write their formulas. Another difference is that two nonmetal atoms will frequently combine with one another in a variety of ratios. Consider the elements nitrogen and oxygen. They combine to make several compounds including:<\/span><\/p>\n<h4><span style=\"color: #000000\"><strong><span class=\"MathJax\" id=\"MathJax-Element-9-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-89\"><span class=\"mrow\" id=\"MathJax-Span-90\"><span class=\"mtext\" id=\"MathJax-Span-91\">NO<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-10-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-92\"><span class=\"mrow\" id=\"MathJax-Span-93\"><span class=\"msubsup\" id=\"MathJax-Span-94\"><span class=\"mtext\" id=\"MathJax-Span-95\">NO<\/span><span class=\"texatom\" id=\"MathJax-Span-96\"><span class=\"mrow\" id=\"MathJax-Span-97\"><span class=\"mspace\" id=\"MathJax-Span-98\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-99\"><span class=\"mrow\" id=\"MathJax-Span-100\"><span class=\"mn\" id=\"MathJax-Span-101\">2<\/span><\/span><\/span><\/sub><\/span><\/span><\/span><\/span>, and <\/strong><span class=\"MathJax\" id=\"MathJax-Element-11-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-102\"><strong><span class=\"mrow\" id=\"MathJax-Span-103\"><span class=\"msubsup\" id=\"MathJax-Span-104\"><span class=\"mtext\" id=\"MathJax-Span-105\">N<\/span><span class=\"texatom\" id=\"MathJax-Span-106\"><span class=\"mrow\" id=\"MathJax-Span-107\"><span class=\"mspace\" id=\"MathJax-Span-108\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-109\"><span class=\"mrow\" id=\"MathJax-Span-110\"><span class=\"mn\" id=\"MathJax-Span-111\">2<\/span><\/span><\/span><\/sub><\/span><span class=\"mtext\" id=\"MathJax-Span-112\">O<\/span><\/span><\/strong><\/span><\/span><\/span><\/h4>\n<p><span style=\"color: #000000\">They all can&#8217;t be called nitrogen oxide. How would someone know which one you were talking about? Each of the three compounds has very different properties and reactivity. A system to distinguish between compounds such as these is necessary.<\/span><\/p>\n<p><span style=\"color: #000000\">Prefixes are used in the names of binary molecular compounds to identify the number of atoms of each element. The table below shows the prefixes up to ten.<\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Table 5.3 Prefixes used for Nomenclature of Binary Covalent Molecules<\/strong><\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/prefix_names-1.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/prefix_names-1.png\" alt=\"\" class=\"alignnone wp-image-3290\" width=\"362\" height=\"421\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/prefix_names-1.png 707w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/prefix_names-1-258x300.png 258w\" sizes=\"(max-width: 362px) 100vw, 362px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">The rules for using the prefix system of nomenclature of binary compounds can be summarized as follows.<\/span><\/p>\n<ol>\n<li><span style=\"color: #000000\">Generally, the less-electronegative element is written first in the formula, though there are a few exceptions. <em>Exception 1<\/em>: Carbon is always first in a formula. <em>Exception 2:<\/em> When hydrogen is participating in a covalent bond, it is typically written in the second postion (For example: hydrogen is after nitrogen in a formula such as <span class=\"MathJax\" id=\"MathJax-Element-13-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-119\"><span class=\"mrow\" id=\"MathJax-Span-120\"><span class=\"msubsup\" id=\"MathJax-Span-121\"><span class=\"mtext\" id=\"MathJax-Span-122\">NH<\/span><span class=\"texatom\" id=\"MathJax-Span-123\"><span class=\"mrow\" id=\"MathJax-Span-124\"><span class=\"mspace\" id=\"MathJax-Span-125\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-126\"><span class=\"mrow\" id=\"MathJax-Span-127\"><span class=\"mn\" id=\"MathJax-Span-128\">3<\/span><\/span><\/span><\/sub><span class=\"texatom\" id=\"MathJax-Span-126\"><span class=\"mrow\" id=\"MathJax-Span-127\"><span class=\"mn\" id=\"MathJax-Span-128\">) Overall, t<\/span><\/span><\/span><\/span><\/span><\/span><\/span>he order of common nonmetals in binary molecular compounds is <span class=\"MathJax\" id=\"MathJax-Element-14-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-129\"><span class=\"mrow\" id=\"MathJax-Span-130\"><span class=\"mtext\" id=\"MathJax-Span-131\">C<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-15-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-132\"><span class=\"mrow\" id=\"MathJax-Span-133\"><span class=\"mtext\" id=\"MathJax-Span-134\">P<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-16-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-135\"><span class=\"mrow\" id=\"MathJax-Span-136\"><span class=\"mtext\" id=\"MathJax-Span-137\">N<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-17-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-138\"><span class=\"mrow\" id=\"MathJax-Span-139\"><span class=\"mtext\" id=\"MathJax-Span-140\">H<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-18-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-141\"><span class=\"mrow\" id=\"MathJax-Span-142\"><span class=\"mtext\" id=\"MathJax-Span-143\">S<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-19-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-144\"><span class=\"mrow\" id=\"MathJax-Span-145\"><span class=\"mtext\" id=\"MathJax-Span-146\">I<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-20-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-147\"><span class=\"mrow\" id=\"MathJax-Span-148\"><span class=\"mtext\" id=\"MathJax-Span-149\">Br<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-21-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-150\"><span class=\"mrow\" id=\"MathJax-Span-151\"><span class=\"mtext\" id=\"MathJax-Span-152\">Cl<\/span><\/span><\/span><\/span>, <span class=\"MathJax\" id=\"MathJax-Element-22-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-153\"><span class=\"mrow\" id=\"MathJax-Span-154\"><span class=\"mtext\" id=\"MathJax-Span-155\">O<\/span><\/span><\/span><\/span>,<\/span><\/li>\n<li><span style=\"color: #000000\"><span class=\"MathJax\" id=\"MathJax-Element-23-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-156\"><span class=\"mrow\" id=\"MathJax-Span-157\"><span class=\"mtext\" id=\"MathJax-Span-158\"><\/span><\/span><\/span><\/span>When naming the first element, use the full name of the element and the appropriate prefix if there are more than one atom of that element in the formula. If there is only one atom for the first element, the term mono- is NOT used, but is implied. For example, CO is carbon monoxide, not monocarbon monoxide.<\/span><\/li>\n<li><span style=\"color: #000000\">For the second element the ending of the element&#8217;s name is typically changed to &#8216;<em>-ide&#8217;\u00a0<\/em>and the appropriate prefix is <strong><em>always<\/em><\/strong> used for the second element.<\/span><\/li>\n<\/ol>\n<p><span style=\"color: #000000\">Note: the\u00a0<em>a<\/em>\u00a0or\u00a0<em>o<\/em>\u00a0at the end of a prefix is usually dropped from the name when the name of the element begins with a vowel. As an example, four oxygen atoms, is tetroxide instead of tetraoxide. Some examples of molecular compounds are listed in Table 5.4<span class=\"MathJax\" id=\"MathJax-Element-24-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-159\"><span class=\"mrow\" id=\"MathJax-Span-160\"><span class=\"texatom\" id=\"MathJax-Span-161\"><span class=\"mrow\" id=\"MathJax-Span-162\"><span class=\"mn\" id=\"MathJax-Span-163\"><\/span><span class=\"mn\" id=\"MathJax-Span-164\">.<\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Table 5.4 Examples of Naming Covalent Molecules<\/strong><\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/examples_covalent_names.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/examples_covalent_names-1024x495.png\" alt=\"\" class=\"alignnone wp-image-3292\" width=\"381\" height=\"184\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/examples_covalent_names-1024x495.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/examples_covalent_names-300x145.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/examples_covalent_names-768x371.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/examples_covalent_names.png 1088w\" sizes=\"(max-width: 381px) 100vw, 381px\" \/><\/a><\/p>\n<p><span><span style=\"color: #000000\">Notice that the\u00a0<em>mono-<\/em>\u00a0prefix is not used with the nitrogen in the first compound, but is used with the oxygen in both of the first two examples. The <span class=\"MathJax\" id=\"MathJax-Element-30-Frame\" role=\"presentation\"><span class=\"math\" id=\"MathJax-Span-221\"><span class=\"mrow\" id=\"MathJax-Span-222\"><span class=\"msubsup\" id=\"MathJax-Span-223\"><span class=\"mtext\" id=\"MathJax-Span-224\">S<\/span><span class=\"texatom\" id=\"MathJax-Span-225\"><span class=\"mrow\" id=\"MathJax-Span-226\"><span class=\"mspace\" id=\"MathJax-Span-227\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-228\"><span class=\"mrow\" id=\"MathJax-Span-229\"><span class=\"mn\" id=\"MathJax-Span-230\">2<\/span><\/span><\/span><\/sub><\/span><span class=\"msubsup\" id=\"MathJax-Span-231\"><span class=\"mtext\" id=\"MathJax-Span-232\">Cl<\/span><span class=\"texatom\" id=\"MathJax-Span-233\"><span class=\"mrow\" id=\"MathJax-Span-234\"><span class=\"mspace\" id=\"MathJax-Span-235\"><\/span><\/span><\/span><sub><span class=\"texatom\" id=\"MathJax-Span-236\"><span class=\"mrow\" id=\"MathJax-Span-237\"><span class=\"mn\" id=\"MathJax-Span-238\">2 <\/span><\/span><\/span><\/sub><\/span><\/span><\/span><\/span>emphasizes that the formulas for molecular compounds are not reduced to their lowest ratios. The\u00a0<em>o<\/em>\u00a0of the\u00a0<em>mono-<\/em>\u00a0and the\u00a0<em>a<\/em>\u00a0of\u00a0<em>hepta-<\/em>\u00a0are dropped from the name when paired with oxide. For example:<\/span><br \/>\n<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/naming-exampmle.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/naming-exampmle.png\" alt=\"\" class=\"alignnone wp-image-3488\" width=\"401\" height=\"346\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/04\/naming-exampmle.png 554w, https:\/\/wou.edu\/chemistry\/files\/2017\/04\/naming-exampmle-300x259.png 300w\" sizes=\"(max-width: 401px) 100vw, 401px\" \/><\/a><\/p>\n<h4><a href=\"#CH103top5\"><span style=\"color: #ff0000\"><strong><em>(back to the top)<\/em><\/strong><\/span><\/a><\/h4>\n<hr \/>\n<h3 id=\"intermolecular\"><strong>5.6 Intermolecular Forces<\/strong><\/h3>\n<p><span style=\"color: #000000\">In addition to learning about how elements join together to form bonds, it is also very important to learn about how molecules interact with other molecules around them. This type of interaction, known as an <strong><em>intermolecular interaction<\/em><\/strong>, is important for determining broader characteristics of the molecule including reactivity and function.<\/span><\/p>\n<p><span style=\"color: #000000\">Intermolecular interactions between molecules are dependent on the phase that the molecule exists.\u00a0 A phase is a certain form of matter that includes a specific set of physical properties. That is, the atoms, the molecules, or the ions that make up the phase do so in a consistent manner throughout the phase. As mentioned in Chapter 2, science recognizes three stable phases: the <strong><em>solid phase<\/em><\/strong>, in which individual particles can be thought of as in contact and held in place (defined volume and shape); the <strong><em>liquid phase<\/em><\/strong>, in which individual particles are in contact but moving with respect to each other (defined volume but, shape of the container); and the <strong><em>gas phase<\/em><\/strong> (no defined shape or volume), in which individual particles are separated from each other by relatively large distances. Not all substances will readily exhibit all phases on the Earth. For example, carbon dioxide does not exhibit a liquid or solid\u00a0phase on Earth unless the pressure is greater than about six times normal atmospheric pressure. Other substances, especially complex organic molecules, may decompose or breakdown at higher temperatures, rather than becoming a liquid or a gas. For example, think about roasting a marshmallow.\u00a0 If it gets too close to the flames it will become\u00a0charred and blackened, breaking down the sugar<\/span> <span style=\"color: #000000\">molecules inside.\u00a0The sugar is not converted into the liquid or gaseous phase. Thus, water is very unique in\u00a0its ability\u00a0to exist on the Earth in all three phase states (solid ice &#8211; liquid water &#8211; water vapor).<\/span><\/p>\n<p><span style=\"color: #000000\">Which phase a substance adopts depends on the pressure and the temperature it experiences. Of these two conditions, temperature variations are more obviously related to the phase of a substance. When it is very cold, H<sub>2<\/sub>O exists in the solid form as ice. When it is warmer, the liquid phase of H<sub>2<\/sub>O is present. At even higher temperatures, H<sub>2<\/sub>O boils and becomes steam (gaseous phase).<\/span><\/p>\n<div>\n<p><span style=\"color: #000000\">Pressure changes can also affect the presence of a particular phase (as we indicated for carbon dioxide), but its effects are less obvious most of the time. We will mostly focus on the temperature effects on phases, mentioning pressure effects only when they are important. Most chemical substances follow the same pattern of phases when going from a low temperature to a high temperature: the solid phase, then the liquid phase, and then the gas phase. However, the temperatures at which these phases are present differ for all substances and can be rather extreme. Table 5.5 shows the temperature ranges for solid, liquid, and gas phases for three substances. As you can see, there is extreme variability in the temperature ranges. Recall that the<strong> <em>melting point<\/em> <\/strong>of a substance is the temperature that separates a solid and a liquid. The<strong> <em>boiling point<\/em> <\/strong>of a substance is the temperature that separates a liquid and a gas.<\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Table 5.5 Each Substance has a Characteristic Melting Point and Boiling Point<\/strong><\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2018\/12\/table-5.5-1.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2018\/12\/table-5.5-1-1024x375.png\" alt=\"\" class=\"alignnone wp-image-4378\" width=\"695\" height=\"255\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2018\/12\/table-5.5-1-1024x375.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2018\/12\/table-5.5-1-300x110.png 300w, https:\/\/wou.edu\/chemistry\/files\/2018\/12\/table-5.5-1-768x281.png 768w, https:\/\/wou.edu\/chemistry\/files\/2018\/12\/table-5.5-1.png 1341w\" sizes=\"(max-width: 695px) 100vw, 695px\" \/><\/a><\/p>\n<div>\n<p><span style=\"color: #000000\">What accounts for this variability? Why do some substances become liquids at very low temperatures, while others require very high temperatures before they become liquids? It all depends on the strength of the intermolecular interactions between the particles of substances. (Although ionic compounds are not composed of discrete molecules, we will still use the term intermolecular to include interactions between the ions in such compounds.) Substances that experience strong intermolecular interactions require higher temperatures to become liquids and, finally, gases. Substances that experience weak intermolecular interactions do not need much energy (as measured by temperature) to become liquids and gases and will exhibit these phases at lower temperatures.<\/span><\/p>\n<p><span style=\"color: #000000\">Intermolecular forces determine bulk properties such as the melting points of solids and the boiling points of liquids. Liquids boil when the molecules have enough thermal energy to overcome the intermolecular attractive forces that hold them together, thereby forming bubbles of vapor within the liquid. Similarly, solids melt when the molecules acquire enough thermal energy to overcome the intermolecular forces that lock them into place in the solid.<\/span><\/p>\n<p><span style=\"color: #000000\">Intermolecular forces are <strong><em>electrostatic<\/em><\/strong> in nature; that is, they arise from the interaction between positively and negatively charged species. Like covalent and ionic bonds, intermolecular interactions are the sum of both attractive and repulsive components. Because electrostatic interactions fall off rapidly with increasing distance between molecules, intermolecular interactions are most important for solids and liquids, where the molecules are close together. These interactions become important for gases only at very high pressures, where they are responsible for the observed deviations from the ideal gas law at high pressures.<\/span><\/p>\n<p><span style=\"color: #000000\">Substances with the highest melting and boiling points have <em>covalent network bonding<\/em>. This type of interaction is actually a covalent bond. In these substances, all the atoms in a sample are covalently bonded to the other atoms; in effect, the entire sample is essentially one large molecule. Many of these substances are solid over a large temperature range because it takes a lot of energy to disrupt all the covalent bonds at once. One example of a substance that shows covalent network bonding is diamond (Figure 5.10), which is a form of pure carbon. At temperatures over 3,500\u00b0C, diamond finally vaporizes into gas-phase atoms.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/diamond.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1878\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/diamond-1024x446.jpg\" width=\"668\" height=\"291\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/diamond-1024x446.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/diamond-300x131.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/diamond-768x334.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/diamond.jpg 2023w\" sizes=\"(max-width: 668px) 100vw, 668px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.10. Diamond.<\/strong> Diamond, a form of pure carbon, has covalent network bonding. It takes a very high temperature\u2014over 3,500\u00b0C\u2014for diamond to leave the solid state.<\/span><br \/>\n<span style=\"color: #000000\">Source: Photo \u00a9 Thinkstock<\/span><\/p>\n<hr \/>\n<\/div>\n<p><span style=\"color: #000000\">For interactions between different molecules, the strongest force between any two particles is the <em>ionic bond<\/em>, in which two ions of opposing charge are attracted to each other. Thus, ionic interactions between particles are\u00a0an intermolecular interaction. Substances that contain ionic interactions are strongly held together, so these substances typically have high melting and boiling points. Sodium chloride (Figure 5.11) is an example of a substance whose particles experience ionic interactions.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/sodium-chloride.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1899\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/sodium-chloride-1024x458.jpg\" width=\"672\" height=\"301\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/sodium-chloride-1024x458.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/sodium-chloride-300x134.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/sodium-chloride-768x343.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/sodium-chloride.jpg 1676w\" sizes=\"(max-width: 672px) 100vw, 672px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.11 Sodium Chloride.<\/strong> Solid NaCl is held together by ionic intermolecular forces.\u00a0 Source: Photo \u00a9 Thinkstock<\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">Many substances that experience covalent bonding exist as discrete molecules and do not engage in covalent network bonding. Thus, most covalently bonded molecules will also experience intermolecular forces.\u00a0 These intermolecular forces are weaker than those found in ionic interactions and depend on the\u00a0polarity of the covalent bond.\u00a0Recall that in polar covalent bonds, the electrons that are shared in a covalent bond are not shared equally between the two atoms in the bond. Typically, the atom displaying higher electronegativity attracts the electrons more strongly than the other, leading to\u00a0the unequal sharing of electrons in the bond. This sets up a permanent dipole within the molecule, where one end of the molecule has a partial negative charge (\u03b4\u2212) and one end has a partial positive charge (\u03b4+). This idea is illustrated in Figure 5.12, which shows a diagram of the covalent bond in hydrogen fluoride (HF).<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-flouride.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1884\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-flouride-1024x104.jpg\" width=\"680\" height=\"69\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-flouride-1024x104.jpg 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-flouride-300x31.jpg 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-flouride-768x78.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-flouride.jpg 1500w\" sizes=\"(max-width: 680px) 100vw, 680px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.12 Polar Covalent Bonds.\u00a0<\/strong> The electrons in the HF molecule are not equally shared by the two atoms in the bond. Because the fluorine atom has nine protons in its nucleus, it attracts the negatively charged electrons in the bond more than the hydrogen atom does with its one proton in its nucleus. Thus, electrons are more strongly attracted to the fluorine atom, leading to an imbalance in the electron distribution between the atoms. The fluorine side of the bond picks up a partial overall negative charge (represented by the \u03b4\u2212 in the diagram), while the hydrogen side of the bond has an overall partial positive charge (represented by the \u03b4+ in the diagram). Such a bond is called a <strong><em>polar covalent bond<\/em><\/strong>.<\/span><\/p>\n<hr \/>\n<\/div>\n<p><span style=\"color: #000000\">The fluorine atom attracts the electrons in the bond more than the hydrogen atom does. The result is an unequal distribution of electrons in the bond, favoring the fluorine side of the covalent bond. Because of this unequal distribution, the fluorine side of the covalent bond actually takes on a partial negative charge (indicated by the \u03b4\u2212 in Figure 5.12), while the hydrogen side of the bond, being electron deficient, takes on a partial positive charge (indicated by the \u03b4+ in Figure 5.12). A covalent bond that has an unequal sharing of electrons is called a polar covalent bond. (A covalent bond that has an equal sharing of electrons, as in a covalent bond with the same atom on each side, is called a nonpolar covalent bond.) A molecule with a net unequal distribution of electrons in its covalent bonds is a polar molecule. HF is an example of a polar molecule.<\/span><\/p>\n<p><span style=\"color: #000000\">The charge separation in a polar covalent bond is not as extreme as is found in ionic compounds, but there is a related result: oppositely charged ends of different molecules will attract each other. This type of intermolecular interaction is called a <em><strong>dipole-dipole<\/strong> <\/em>interaction. If the structure of a molecule is polar, then the molecule has a net dipole moment. Molecules with net dipole moments tend to align themselves so that the positive end of one dipole is near the negative end of another and vice versa, as shown in part (a) in Figure 5.13. These arrangements are more stable than arrangements in which two positive or two negative ends are adjacent (Figure 5.13, part c). Hence dipole\u2013dipole interactions, such as those in part (b) in Figure 5.13, are attractive intermolecular interactions, whereas those in part (d) in Figure 5.13 are repulsive intermolecular interactions. Because molecules in a liquid move freely and continuously, molecules always experience both attractive and repulsive dipole\u2013dipole interactions simultaneously, as shown in Figure 5.14. On average, however, the attractive interactions dominate.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dipole-dipole-interactions.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1879\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dipole-dipole-interactions-849x1024.jpg\" width=\"674\" height=\"813\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dipole-dipole-interactions-849x1024.jpg 849w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dipole-dipole-interactions-249x300.jpg 249w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dipole-dipole-interactions-768x927.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dipole-dipole-interactions.jpg 1050w\" sizes=\"(max-width: 674px) 100vw, 674px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.13 Attractive and Repulsive Dipole-Dipole Interactions.<\/strong> (a and b) Molecular orientations in which the positive end of one dipole (\u03b4+) is near the negative end of another (\u03b4\u2212) (and vice versa) produce attractive interactions. (c and d) Molecular orientations that juxtapose the positive or negative ends of the dipoles on adjacent molecules produce repulsive interactions.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/both-attractive-and-repulsive.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1873\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/both-attractive-and-repulsive-938x1024.jpg\" width=\"677\" height=\"739\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/both-attractive-and-repulsive-938x1024.jpg 938w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/both-attractive-and-repulsive-275x300.jpg 275w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/both-attractive-and-repulsive-768x838.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/both-attractive-and-repulsive.jpg 1058w\" sizes=\"(max-width: 677px) 100vw, 677px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.14 Both Attractive and Repulsive Dipole-Dipole Interactions Occur in a Liquid Sample with Many Molecules.<\/strong><\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">The H\u2013F, O\u2013H, and N\u2013H bonds are strongly polar; In molecules that have these bonds, particularly strong dipole-dipole interactions (as strong as 10% of a true covalent bond) can occur. Because of this strong interaction, <em><strong>hydrogen bonding<\/strong><\/em> is used to describe this dipole-dipole interaction. The physical properties of water, which has two O\u2013H bonds, are strongly affected by the presence of hydrogen bonding between water molecules. Figure 5.15 shows how molecules experiencing hydrogen bonding can interact in water.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-boinding.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1883\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-boinding-942x1024.jpg\" width=\"684\" height=\"744\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-boinding-942x1024.jpg 942w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-boinding-276x300.jpg 276w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-boinding-768x835.jpg 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hydrogen-boinding.jpg 1069w\" sizes=\"(max-width: 684px) 100vw, 684px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.15 Hydrogen Bonding between Water Molecules.<\/strong> The presence of hydrogen bonding in molecules like water can have a large impact on the physical properties of a substance.<\/span><\/p>\n<hr \/>\n<div>\n<p><span style=\"color: #000000\">Finally, there are forces between all molecules that are caused by electrons being in different places in a molecule at any one time, which sets up a temporary separation of charge that disappears almost as soon as it appears and sets up a momentary &#8216;induced dipole&#8217;. These are very weak intermolecular interactions and are called <strong><i>London dispersion forces<\/i>. <\/strong>Since electrons naturally orbit the nucleus of the atom, there are momentary dipoles that are present in the atom as the electrons are shifting from one side to the other.\u00a0 If other atoms are in close proximity, the electrons of the other atoms will orbit in concert with the neighboring atom, i.e. the electrons of one atom are repulsive to the electrons of the neighboring atoms, such that when they are close to the neighboring atom, the neighboring electrons will shift away to the other side of the atom. Thus, the electon movements between atoms of different molecules will synchronize and orbit in a pattern that maximizes the distance between electrons of a neighboring atom. Note that all substances experience London dispersion forces.\u00a0 However, these are the only intermolecular forces that nonpolar covalent compounds experience. Nonpolar covalent molecules tend to be soft in the solid phase and have relatively low melting points. Butter fat would be a good example of a nonpolar covalent compound.<\/span><\/p>\n<p><span style=\"color: #000000\">Because London dispersion forces are caused by the instantaneous distribution of electrons in a molecule, larger molecules with a large number of electrons can experience\u00a0higher levels of\u00a0London dispersion forces. Examples include waxes, which are long hydrocarbon chains that are solids at room temperature because the molecules have so many electrons. The resulting dispersion forces between these molecules make them assume the solid phase at normal temperatures.<\/span><\/p>\n<hr \/>\n<h4><a href=\"https:\/\/www.youtube.com\/watch?v=1iYKajMsYPY\"><span style=\"color: #ff0000\"><strong>Video Tutorial on London Dispersion Forces By Bozeman Science.<\/strong><\/span><\/a><\/h4>\n<hr \/>\n<p><span style=\"color: #000000\">The phase that a substance adopts depends on the type and magnitude of the intermolecular interactions the particles of a substance experience. If the intermolecular interactions are relatively strong, then a large amount of energy\u2014in terms of temperature\u2014is necessary for a substance to change phases. If the intermolecular interactions are weak, a low temperature is all that is necessary to move a substance out of the solid phase. Overall, Ionic interactions are the strongest intermolecular forces followed by hydrogen bonding, other dipole-dipole interactions, and lastly, induced dipoles (London dispersion forces).\u00a0 Intermolecular force strength is indicated in Table 5.6.<\/span><\/p>\n<h4><span style=\"color: #000000\"><strong>Table 5.6 Strength of Intermolecular Forces<\/strong><\/span><\/h4>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/table_4.3-1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-1947\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/table_4.3-1.png\" width=\"714\" height=\"232\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/table_4.3-1.png 714w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/table_4.3-1-300x97.png 300w\" sizes=\"(max-width: 714px) 100vw, 714px\" \/><\/a><\/p>\n<p><span><span style=\"color: #000000\">Source:<\/span> <a href=\"https:\/\/en.wikipedia.org\/wiki\/Intermolecular_force\">https:\/\/en.wikipedia.org\/wiki\/Intermolecular_force<\/a><\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/example-IMF.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1950\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/example-IMF.jpg\" width=\"684\" height=\"912\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/example-IMF.jpg 720w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/example-IMF-225x300.jpg 225w\" sizes=\"(max-width: 684px) 100vw, 684px\" \/><\/a><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/skillbuilding_IMF.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1951\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/skillbuilding_IMF.png\" width=\"686\" height=\"301\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/skillbuilding_IMF.png 766w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/skillbuilding_IMF-300x132.png 300w\" sizes=\"(max-width: 686px) 100vw, 686px\" \/><\/a><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Exercises-IMF.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1952\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Exercises-IMF.jpg\" width=\"689\" height=\"919\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Exercises-IMF.jpg 720w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/Exercises-IMF-225x300.jpg 225w\" sizes=\"(max-width: 689px) 100vw, 689px\" \/><\/a><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/exercise_IMP_Odd_Answ.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-1953\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/exercise_IMP_Odd_Answ.png\" width=\"680\" height=\"446\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/exercise_IMP_Odd_Answ.png 767w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/exercise_IMP_Odd_Answ-300x197.png 300w\" sizes=\"(max-width: 680px) 100vw, 680px\" \/><\/a><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(BACK TO THE TOP)<\/strong><\/em><\/span><\/a><\/p>\n<\/div>\n<h3 id=\"drawing\"><strong>5.7 Recognizing and Drawing Organic Molecules<br \/>\n<\/strong><\/h3>\n<p><span style=\"color: #000000\">As noted in section 5.1, organic compounds are compounds that contain carbon and hydrogen.\u00a0 Another notable feature of organic molecules is that they are quite complex and contain many atoms of carbon and hydrogen as well as other <strong><em>heteroatoms<\/em><\/strong> (atoms other than carbon or hydrogen) that are held together through covalent bonding. The most common <strong><em>heteroatoms<\/em><\/strong> that will be found in organic molecules include oxygen, nitrogen, sulfur, phosphorous, and occasionally halides (Cl, Br, and I). Since they can be quite complex, it is useful to discuss the many different ways that organic compounds can be represented\/drawn.<\/span><\/p>\n<h4><span style=\"color: #ff0000\"><strong>Molecular Formula<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">A <em><strong>molecular formula<\/strong><\/em> is the simplest way to represent a compound by counting up all of the different types of atoms and listing them\u00a0in order.\u00a0 For example,\u00a0the sugar\u00a0glucose, contains 6 carbons, 12 hydrogens, and 6 oxygens. The molecular formula would then be\u00a0written as C<sub>6<\/sub>H<sub>12<\/sub>O<sub>6<\/sub>. By convention, carbon is listed first, hydrogen second, followed by oxygen, nitrogen, sulfur, phosphorus, and finally any halogens.\u00a0However, for organic chemistry,\u00a0molecular formulae\u00a0don&#8217;t provide much information.\u00a0 They simply\u00a0provide the numbers of each\u00a0type of atom present in the molecule, but they tell\u00a0you nothing about the way the atoms are joined together in space. For example, two molecules might have the same molecular formula, but a different arrangement of the atoms bonded in space, as is the case for the two sugars glucose and fructose. Both sugars have the molecular formula of C<sub>6<\/sub>H<sub>12<\/sub>O<sub>6<\/sub>. However, you can see from Figure 5.16, that they are different molecules with different properties, because the atoms are linked together in a different order. Molecules that share the same molecular formula but have their atoms bonded in a different order are called <em><strong>isomers<\/strong><\/em>. Due to the complexity of isomer structures, molecular formulae not as often used in organic chemistry, because they do not give useful information about the bonding order within the molecule.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2018\/12\/glucose-fructose.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2018\/12\/glucose-fructose.png\" alt=\"\" class=\"alignnone wp-image-4323\" width=\"473\" height=\"386\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2018\/12\/glucose-fructose.png 609w, https:\/\/wou.edu\/chemistry\/files\/2018\/12\/glucose-fructose-300x245.png 300w\" sizes=\"(max-width: 473px) 100vw, 473px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.16 Structural Isomers.<\/strong>\u00a0 When molecules, such as D-Glucose and D-Fructose, share the same molecular formula, but have a different atomic bonding order they are called structural isomers.<\/span><\/p>\n<hr \/>\n<div class=\"mt-section\" id=\"section_2\">\n<h4 id=\"structuralform\"><span><strong>Structural formulae and 3-dimensional models<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">A structural formula shows how the various atoms are bonded, and can be more useful that only writing the molecular formula for a compound. There are various ways of drawing\u00a0structural formulae\u00a0and you will need to be familiar with all of them. They include the <em><strong>displayed formula, condensed formulas<\/strong>,<\/em> and <em><strong>line structures<\/strong>.<\/em><\/span><\/p>\n<\/div>\n<div class=\"mt-section\" id=\"section_3\">\n<h5 class=\"editable\"><span><em>Displayed formulae<\/em><\/span><\/h5>\n<p><span style=\"color: #000000\">A <strong><em>displayed formula<\/em><\/strong> shows all the bonds in the molecule as individual lines with each atom written at the end of each line using its elemental abbreviation from the periodic table. The structures of C<sub>6<\/sub>H<sub>12<\/sub>O<sub>6<\/sub>, above,\u00a0are all written in <strong><em>displayed formulae<\/em>.<\/strong> You need to remember that each line represents a pair of shared electrons. For example,\u00a0figure 5.17 below depicts the displayed formula of methane next to the three-dimensional representations.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/methane.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2035\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/methane-1024x384.png\" width=\"586\" height=\"220\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/methane-1024x384.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/methane-300x113.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/methane-768x288.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/methane.png 1031w\" sizes=\"(max-width: 586px) 100vw, 586px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.17: Three different representations of CH<sub>4<\/sub><\/strong> On the left is the ball and stick model, in the center is the displayed formula, and to the right is the space-filling model.<\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">Notice that the\u00a0displayed formula\u00a0of methane does not represent the 3-D shape of the molecule shown in the space-filling diagram on the right. Methane isn&#8217;t flat with 90\u00b0 bond angles. This mismatch between what you draw and what the molecule actually looks like can lead to problems if you aren&#8217;t careful. Thus, for organic chemistry, it is important to begin thinking about the structures in their 3-D form.\u00a0 The more you practice, the more you will be able to visualize and turn the molecule around in your head.\u00a0 For example, consider the simple molecule with the molecular formula CH<sub>2<\/sub>Cl<sub>2<\/sub>. You might think that there were two different ways of arranging these atoms if you drew a displayed formula.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dichloromethane.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-2041\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dichloromethane.png\" width=\"463\" height=\"217\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dichloromethane.png 463w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dichloromethane-300x141.png 300w\" sizes=\"(max-width: 463px) 100vw, 463px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">But these two structures are actually exactly the same. When atoms are sharing electrons with other atoms, they tend to take on three dimensional spatial relationships that keep the electrons in shared pairs as far away as possible from other electrons in shared pairs.\u00a0 This tendency is called valence shell electron pair repulsion theory or VESPR. Due to this tendency, since carbon forms four bonds, it will take on a tetrahedral confirmation where each bond angle\u00a0is 109<sup><sub>o<\/sub><\/sup>.\u00a0 The molecule is not flat, in the plane of the paper.\u00a0Play the video below to\u00a0see how they appear as rotating\u00a0ball and stick models.<\/span><\/p>\n<div style=\"width: 584px;\" class=\"wp-video\"><video class=\"wp-video-shortcode\" id=\"video-4291-4\" width=\"584\" height=\"468\" preload=\"metadata\" controls=\"controls\"><source type=\"video\/mp4\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dichloromethane-spinning.mp4?_=4\" \/><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dichloromethane-spinning.mp4\">https:\/\/wou.edu\/chemistry\/files\/2017\/01\/dichloromethane-spinning.mp4<\/a><\/video><\/div>\n<p><span style=\"color: #000000\">One structure is in reality a simple rotation of the other one. Consider a slightly more complicated molecule, C<sub>2<\/sub>H<sub>5<\/sub>Cl. The displayed formula could be written as either of these:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chloroethane.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-2046\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chloroethane.png\" width=\"560\" height=\"218\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chloroethane.png 560w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chloroethane-300x117.png 300w\" sizes=\"(max-width: 560px) 100vw, 560px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">But, again these are exactly the same. Look at the models below.<\/span><\/p>\n<div style=\"width: 584px;\" class=\"wp-video\"><video class=\"wp-video-shortcode\" id=\"video-4291-5\" width=\"584\" height=\"468\" preload=\"metadata\" controls=\"controls\"><source type=\"video\/mp4\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chloroethane-spinning.mp4?_=5\" \/><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chloroethane-spinning.mp4\">https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chloroethane-spinning.mp4<\/a><\/video><\/div>\n<p><span style=\"color: #000000\">As you continue to practice drawing out structural formulae, you will become better\u00a0at recognizing and distinguishing between isomers that are truly different from one another, and versions of\u00a0the same molecule written drawn from different 3-dimensional perspectives.<\/span><\/p>\n<\/div>\n<div class=\"mt-section\" id=\"section_4\">\n<h5 class=\"editable\"><span style=\"color: #ff0000\"><em>Condensed formulae<\/em><\/span><\/h5>\n<p><span style=\"color: #000000\">For anything other than the most simple molecules, drawing a fully displayed formula\u00a0can be cumbersome and take up too much space\u00a0&#8211; especially all the carbon-hydrogen bonds. You can simplify &#8211; or <em>condense &#8211;\u00a0<\/em>the formula by writing, for example, CH<sub>3<\/sub> or CH<sub>2<\/sub> instead of showing all the C-H\u00a0bonds. For example, ethanoic (C<sub>2<\/sub>H<sub>4<\/sub>O<sub>2<\/sub>)\u00a0acid\u00a0can\u00a0be shown in a fully displayed form, a partially condensed form and a fully condensed form.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structures.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2052\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structures.png\" width=\"648\" height=\"182\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structures.png 915w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structures-300x84.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structures-768x216.png 768w\" sizes=\"(max-width: 648px) 100vw, 648px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Notice that the partially condensed structure still provides a very clear picture of where each of the atoms is bonded in space. However, with the fully condensed structure, it\u00a0can be challenging to accurately see the bonding patterns.\u00a0 The fully condensed form\u00a0does contain more information about bonding order than\u00a0the molecular formula,\u00a0such that the atoms that are directly bonded to a neighboring atom are placed adjacent to that atom in the condensed form, rather than a\u00a0simple tallying of\u00a0the total atom species as in the molecular formula.<\/span><\/p>\n<\/div>\n<p><span style=\"color: #000000\">By working backwards, we can use the condensed structure\u00a0of ethanoic acid as an example to recreate the partially condensed structure.\u00a0 When looking at the first carbon position, it is apparent\u00a0that there\u00a0are three hydrogens and one carbon bound to the first carbon:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structure-2.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2055\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structure-2.png\" width=\"128\" height=\"89\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Note that this satisfies the octet rule for the first carbon (four bonds\u00a0to other atoms).\u00a0 The three hydrogens are also complete with their single bonds to the first carbon.\u00a0 The second carbon has now been assigned one bond\u00a0to the first carbon.\u00a0 We need to assign the remaining three bonds.<\/span><\/p>\n<p><span style=\"color: #000000\">From the condensed formula, it is clear that the first oxygen is attached to the second carbon, however, after that, we become unsure about the position of the second oxygen.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structure-3.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2056\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-structure-3.png\" width=\"121\" height=\"69\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">We can clearly\u00a0deduce that the last hydrogen atom is bound to the second oxygen, as it is placed in that position.\u00a0 However, because oxygen can form two bonds, we can&#8217;t be sure based on the condensed structure alone, that the second oxygen is bound to the second carbon or to the first oxygen.<\/span><\/p>\n<p><span style=\"color: #000000\">When you are unsure of which atom is bonded to which, it is best to draw out the potential structures and evaluate them for their potential correctness.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-6.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2062\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-6.png\" width=\"669\" height=\"343\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-6.png 727w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/condensed-6-300x154.png 300w\" sizes=\"(max-width: 669px) 100vw, 669px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">From the analysis of the potential structures above, it is clear that neither structure satisfies the octet rule for one or more atoms within the molecule as currently written.\u00a0 However, the lower structure is less satisfactory than the upper structure, as the second carbon is missing 2 covalent bonds while all of the other atoms have satisfied the octet\u00a0bonding requirements.\u00a0 In the upper diagram, both the second carbon and the first oxygen atom are lacking one bond.\u00a0 This structure can easily satisfy the octet rule by placing a double bond between carbon 2 and oxygen 1 within the molecule. Whereas, a solution for the missing two carbon bonds for the second carbon in the lower structure is not easily remedied. Thus, the upper structure is a more probable structure than the lower structure with the addition of the double bond between the carbon and the oxygen.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/acetic-acid.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2345\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/acetic-acid.png\" width=\"222\" height=\"144\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">While condensed structures are easier to write than displayed or partially condensed structures they can prove to be a little more challenging to determine the three dimensional bonding pattern of the atoms.<\/span><\/p>\n<h4 id=\"line\"><span><em><strong>Line or Skeletal\u00a0Formulae<\/strong><\/em><\/span><\/h4>\n<p><span style=\"color: #000000\">In a <strong><em>line or skeletal formula<\/em><\/strong>, all the hydrogen atoms are not shown\u00a0and all the carbons are not labeled but rather are indicated at the end or bend in every line, leaving just a carbon skeleton with functional groups attached to it.\u00a0Any <strong><em>heteroatoms<\/em><\/strong> (any other atom than carbon\u00a0or hydrogen) and hydrogens attached to\u00a0heteroatoms are shown in condensed form.\u00a0For example, the displayed structure, partially condensed structure\u00a0and the\u00a0line formula for 2-butanol (C<sub>4<\/sub>H<sub>10<\/sub>O) look like this:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/displayed-to-line-structure.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2094\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/displayed-to-line-structure-1024x296.png\" width=\"681\" height=\"197\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/displayed-to-line-structure-1024x296.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/displayed-to-line-structure-300x87.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/displayed-to-line-structure-768x222.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/displayed-to-line-structure.png 1038w\" sizes=\"(max-width: 681px) 100vw, 681px\" \/><\/a><\/p>\n<p><span>\u00a0<\/span><\/p>\n<p><span style=\"color: #000000\">In a line or skeletal diagram, the following assumptions can be made:<\/span><\/p>\n<ul>\n<li><span style=\"color: #000000\">there is a carbon atom at each line\u00a0junction and at the end of each\u00a0line.<\/span><\/li>\n<li><span style=\"color: #000000\">there are enough hydrogen atoms attached to each carbon to make the total number of bonds on that carbon equal to 4.<\/span><\/li>\n<li><span style=\"color: #000000\">all heteroatoms (and hydrogens attached to heteroatoms) are shown in condensed format on the skeletal structure.<\/span><\/li>\n<\/ul>\n<p><span style=\"color: #000000\">Within organic chemistry and biochemistry, scientists tend to use a combination of these different formats to represent chemical structures.\u00a0 It is important to become familiar with drawing and interpreting all the different possible representations.<\/span><\/p>\n<h4><a href=\"#CH103top5\"><span style=\"color: #ff0000\"><em><strong>(back to the top)<\/strong><\/em><\/span><\/a><\/h4>\n<hr \/>\n<div class=\"mt-section\" id=\"section_5\">\n<h5 class=\"editable\"><span style=\"color: #ff0000\"><em>How to draw structural formulae in 3-dimensions<\/em><\/span><\/h5>\n<p><span style=\"color: #000000\">There are occasions when it is important to be able to show the precise 3-D arrangement in parts of some molecules when using a structural representation.\u00a0To do this, the bonds are shown using conventional symbols:<\/span><\/p>\n<p><span>\u00a0<a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonds_in_3-D.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2018\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonds_in_3-D.png\" width=\"537\" height=\"97\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonds_in_3-D.png 615w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/bonds_in_3-D-300x54.png 300w\" sizes=\"(max-width: 537px) 100vw, 537px\" \/><\/a><\/span><\/p>\n<p><span style=\"color: #000000\">For example, you might want to show the 3-D arrangement of the groups around the carbon which has the -OH group in 2-butanol.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-4.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2120\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-4-898x1024.png\" width=\"644\" height=\"734\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-4-898x1024.png 898w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-4-263x300.png 263w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-4-768x875.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-4.png 1051w\" sizes=\"(max-width: 644px) 100vw, 644px\" \/><\/a><\/p>\n<p><a href=\"#chapter5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h4 id=\"abbrev\"><span><strong>Drawing abbreviated organic structures<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">Often when drawing organic structures, chemists find it convenient to use the letter &#8216;R&#8217; to designate part of a molecule outside of the region of interest.\u00a0 If we just want to refer in general to a functional group without drawing a specific molecule, for example, we can use &#8216;R groups&#8217; to focus attention on the group of interest:<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63571\/fig1-2-32.png?revision=1\" width=\"612\" height=\"131\" \/><\/p>\n<p><span style=\"color: #000000\">The R group is a convenient way to abbreviate the structures of large biological molecules, especially when we are interested in something that is occurring specifically at one location on the molecule.\u00a0 For example, in chapter 15 when we look at biochemical oxidation-reduction reactions involving the flavin molecule, we will abbreviate a large part of the flavin structure (ie.\u00a0 R = FAD)\u00a0which does not change at all in the reactions of interest:<\/span><\/p>\n<p><span><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63572\/fig1-2-33.png?revision=1\" width=\"688\" height=\"343\" \/><\/span><\/p>\n<p><span style=\"color: #000000\">As an alternative, we can use a &#8216;break&#8217; symbol to indicate that we are looking at a small piece or section of a larger molecule.\u00a0 This is used commonly in the context of drawing groups on large polymers such as proteins or DNA.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63573\/fig1-2-34.png?revision=1\" width=\"573\" height=\"225\" \/><\/p>\n<p><span style=\"color: #000000\">Finally, R groups can be used to concisely illustrate a series of related compounds, such as the family of penicillin-based antibiotics.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63574\/fig1-2-35.png?revision=1\" width=\"655\" height=\"397\" \/><\/p>\n<p><span style=\"color: #000000\">Using abbreviations appropriately is a very important skill to develop when studying organic chemistry in a biological context, because although many biomolecules are very large and complex (and take forever to draw!), usually we are focusing on just one small part of the molecule where a change is taking place.<\/span><\/p>\n<div id=\"note\">\n<p><span style=\"color: #000000\">As a rule, <em>you should never abbreviate any atom involved in a bond-breaking or bond-forming event<\/em> <em>that is being illustrated: <\/em>only abbreviate that part of the molecule which is not involved in the reaction of interest.<\/span><\/p>\n<\/div>\n<p><span style=\"color: #000000\">For example, carbon #2 in the reactant\/product below most definitely is involved in bonding changes, and therefore should not be included in the &#8216;R&#8217; group.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63575\/fig1-2-36.png?revision=1\" width=\"680\" height=\"450\" \/><\/p>\n<p><span style=\"color: #000000\">If you are unsure whether to draw out part of a structure or abbreviate it, the safest thing to do is to draw it out.<\/span><\/p>\n<h4><a href=\"#CH103top5\"><span style=\"color: #ff0000\"><strong><em>(back to the top)<\/em><\/strong><\/span><\/a><\/h4>\n<hr \/>\n<div class=\"mt-section\" id=\"section_6\">\n<div class=\"mt-section\" id=\"section_5\">\n<h3 id=\"chirality\"><strong><span>5.8 Stereoisomers, Enantiomers, and Chirality<\/span><\/strong><\/h3>\n<\/div>\n<div class=\"mt-section\" id=\"section_6\">\n<p><span style=\"color: #000000\">As seen in section 5.7, organic chemistry involves infinitely varied structures arising from how\u00a0the atoms are assembled in\u00a03-dimensional space.\u00a0Providing only\u00a0the\u00a0molecular formula of a compound is often insufficient for defining the compound as many molecular formulas have numerous structural isomers. For example, the\u00a0molecular formula C<sub>2<\/sub>H<sub>6<\/sub>O, a molecule of only 9 atoms, can refer to dimethyl ether or ethanol, depending on whether the oxygen is in the middle of or at the end of the carbon chain.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/ethanol-ether-1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2103\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/ethanol-ether-1.png\" width=\"578\" height=\"159\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/ethanol-ether-1.png 880w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/ethanol-ether-1-300x83.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/ethanol-ether-1-768x211.png 768w\" sizes=\"(max-width: 578px) 100vw, 578px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Remember that <strong><em>structural isomers<\/em> <\/strong>have the same molecular formula, but the order that the atoms are linked together is different, leading to different physical and chemical properties. For example, ethanol is liquid at room temperature, whereas diethyl ether is a gas.<\/span><\/p>\n<p><span style=\"color: #000000\">If the atoms of compounds with the same molecular formula are linked together in the same order, but their 3-dimensional\u00a0arrangement in space differs, they are considered to be a special type of isomer called a <em><strong>stereoisomer<\/strong>.<\/em> The sugar molecules glucose and galactose are stereoisomers.\u00a0 They differ in the spatial position of a single -OH group as indicated in the diagram below:<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/glucose-galactose.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2114\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/glucose-galactose.png\" width=\"500\" height=\"312\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/glucose-galactose.png 813w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/glucose-galactose-300x187.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/glucose-galactose-768x479.png 768w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/><\/a><\/p>\n<\/div>\n<div class=\"mt-section\" id=\"section_6\">\n<p><span style=\"color: #000000\">There is a special\u00a0kind of stereoisomers, called <strong><em>enantiomers<\/em><\/strong>,\u00a0that\u00a0are mirror images of each other, but are not superimposable. This means that no matter how you turn them in space that you can never put them on top of one another and recover the same compound.\u00a0 One example is 2-butanol\u00a0which can be drawn as a pair of enantiomers (Fig. 5.18).<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-5.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2121\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-5.png\" width=\"521\" height=\"622\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-5.png 640w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/enantiomers-5-251x300.png 251w\" sizes=\"(max-width: 521px) 100vw, 521px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.18: The enantiomers of 2-butanol.<\/strong> The enantiomers are shown in the 3-D structural formula displayed\u00a0in the top diagram and the ball and stick model in the lower diagram.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/courses\/online-chemistry-textbooks\/ch103-allied-health-chemistry\/ch103-chapter-5-covalent-bonds-organic-functional-groups-and-biological-molecules\/\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h4 id=\"chiral\"><span><strong>Chirality<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">Enantiomers are said to have the property of <strong>c<em>hirality<\/em>.\u00a0<em>Chirality<\/em><\/strong> is the term that is given to objects that are mirror images but are not superimposable. The term \u2018chiral\u2019 is derived from the Greek word for \u2018handedness\u2019 \u2013 ie. right-handedness or left-handedness.\u00a0 Your hands are chiral: your right hand is a mirror image of your left hand, but if you place one hand on top of the other, both palms down, you see that they are not superimposable. (Fig 5.19). Thus\u00a0chiral\u00a0objects are mirror images of one another, but\u00a0cannot be\u00a0superimposed on top of one another. Carbon becomes chiral when it has four different substituents attached to it. You will notice in the example above that the central carbon has four different groups attached to it:\u00a0 an -OH group, an -H, a\u00a0-CH<sub>3<\/sub>, and a\u00a0-CH<sub>2<\/sub>CH<sub>3 <\/sub>group.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hands.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2118\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hands.png\" width=\"545\" height=\"370\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hands.png 765w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/hands-300x204.png 300w\" sizes=\"(max-width: 545px) 100vw, 545px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.19:\u00a0The Nature of Chirality.\u00a0<\/strong> Carbon becomes chiral when it\u00a0has four different substituents bonded to it. Any way you rotate the molecule on the left, you cannot superimpose it onto the molecule on the right.<\/span><\/p>\n<p><span style=\"color: #000000\">Source:<\/span>\u00a0 <a title=\"File:Chirality with hands.jpg\" href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Chirality_with_hands.jpg\"><span>Chirality with hands.jpg<\/span><\/a>: <span><span style=\"color: #000000\"><span lang=\"en\">Unknown<\/span> derivative work:<\/span> &#8212;<\/span> <a title=\"User:Perhelion\" href=\"https:\/\/commons.wikimedia.org\/wiki\/User:Perhelion\"><i><span>\u03c0\u03f5\u03c1<\/span><\/i><span>\u03ae\u03bb\u03b9\u03bf<\/span><\/a> <a title=\"User talk:Perhelion\" href=\"https:\/\/commons.wikimedia.org\/wiki\/User_talk:Perhelion\"><span>\u2117<\/span><\/a> &#8211; <span class=\"mw-mmv-source\"><a title=\"File:Chirality with hands.jpg\" href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Chirality_with_hands.jpg\"><span>Chirality with hands.jpg<\/span><\/a><\/span><\/p>\n<hr \/>\n<p class=\"mw-mmv-source\"><span style=\"color: #000000\">Stereoisomers that are not enantiomers, such as glucose and galactose shown above,\u00a0<em>do<\/em> have chiral centers and are not superimposable, but they are not mirror images of one another. Only stereoisomers that are also mirror images and not superimposable are termed <strong><em>enantiomers<\/em><\/strong>.\u00a0 <strong><em>Enantiomers<\/em><\/strong> are very hard to separate from one another.\u00a0\u00a0They are nearly identical in their physical and chemical properties. They have the same molecular weight, the same polarity, the same melting and boiling points, etc.\u00a0In fact, enantiomers are\u00a0so alike that they even share the same name! In Figure 5.14 the two enantiomers of 2-butanol are shown.\u00a0 Both of the molecules are 2-butanol.\u00a0 But they are <em>not<\/em>\u00a0exactly the same molecule, in the same way that your left shoe is not <em>exactly<\/em> the same as your right. They are non-superimposable mirror images of each other. How do we communicate this difference?<\/span><\/p>\n<p class=\"mw-mmv-source\"><span style=\"color: #000000\">One small difference between enantiomers is\u00a0the\u00a0direction that\u00a0polarized light will rotate when it hits the molecule. One enantiomer will rotate light in the clockwise direction,\u00a0while the other will rotate it in the counterclockwise direction.\u00a0The clockwise version is termed &#8216;D&#8217; for dextrorotary (or right-handed) and the counterclockwise version is termed &#8216;L&#8217; for levorotary (or left-handed). However,\u00a0light rotation\u00a0cannot be used in a predictive way to determine the absolute stereo-configuration of a molecule\u00a0(i.e. you cannot tell which enantiomer is going to rotate the light to the right or to the left until you actually do the experiment).<\/span><\/p>\n<p class=\"mw-mmv-source\"><span style=\"color: #000000\">Thus, another system is needed to describe the absolute configuration.\u00a0\u00a0The Cahn-Ingold-Prelog (CIP)\u00a0priority system was designed to\u00a0determine the absolute stereo-configuration of\u00a0enantiomers\u00a0as either sinister (S) or rectus (R). In this system, the groups that are attached to the chiral carbon are given priority based on their atomic number (<em>Z<\/em>).\u00a0 Atoms with higher atomic number (more protons) are given higher priority (i.e. S\u00a0 &gt; P &gt; O &gt; N &gt; C &gt; H).<\/span><\/p>\n<p class=\"mw-mmv-source\"><span style=\"color: #000000\">For determining the stereochemistry, place the lowest priority group away from you, so that the other three groups are held\u00a0are facing you. <\/span><span style=\"color: #000000\">Assign priority to the remaining groups.<\/span><\/p>\n<p><span style=\"color: #000000\">The rules for this system of stereochemical nomenclature are, on the surface, fairly simple.\u00a0 We\u2019ll use the simple 3-carbon sugar glyceraldehyde as our first\u00a0example.\u00a0\u00a0Try making a\u00a0model of the stereoisomer of glyceraldehyde\u00a0shown below.\u00a0 If you don&#8217;t have a chemistry modeling kit, an easy alternative is to use toothpicks and gumdrops.\u00a0\u00a0Be sure that you are making the correct enantiomer!<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image096.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4852\/image096.png?revision=1\" width=\"137\" height=\"197\" \/><\/p>\n<p><span style=\"color: #000000\">The first thing that we must do is to assign a <strong>priority<\/strong> to each of the four substituents bound to the <strong>chiral carbon<\/strong>.\u00a0 In this nomenclature system, the priorities are based on atomic number, with higher atomic numbers having a higher priority. We first look at the atoms that are directly bonded to the chiral carbon: these are H, O (in the hydroxyl), C (in the aldehyde), and C (in the CH<sub>2<\/sub>OH group).<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image098.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4854\/image098.png?revision=1\" width=\"697\" height=\"163\" \/><\/p>\n<p><span style=\"color: #000000\">Two priorities are easy: hydrogen, with an atomic number of 1, is the lowest (#4) priority, and the hydroxyl oxygen, with atomic number 8, is priority #1.\u00a0 Carbon has an atomic number of 6.\u00a0 Which of the two \u2018C\u2019 groups is priority #2, the aldehyde (CHO) or the alcohol (CH<sub>2<\/sub>OH)?\u00a0 To determine this, we move one more bond away from the stereocenter: for the aldehyde we have a <em>double<\/em> bond to an oxygen, while on the CH<sub>2<\/sub>OH group we have a <em>single<\/em> bond to an oxygen.\u00a0 If the atom is the same, double bonds have a higher priority than single bonds.\u00a0 Therefore, the aldehyde group is assigned #2 priority and the CH<sub>2<\/sub>OH group the #3 priority.\u00a0 With our priorities assigned, we next make sure that the #4 priority group (the hydrogen) is pointed back away from ourselves, into the plane of the page (it is already).<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image100.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4856\/image100.png?revision=1\" width=\"622\" height=\"228\" \/><\/p>\n<p><span style=\"color: #000000\">Then, we trace a circle defined by the #1, #2, and #3 priority groups, in increasing order.\u00a0 For our glyceraldehyde example, this circle is clockwise, which tells us that this carbon has the \u2018R\u2019 configuration, and that this molecule is (R)-glyceraldehyde. For (S)-glyceraldehyde, the circle described by the #1, #2, and #3 priority groups is counter-clockwise (but first, we\u00a0must flip the molecule over so that the H is pointing into the plane of the page).<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image102.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4858\/image102.png?revision=1\" width=\"501\" height=\"184\" \/><\/p>\n<p class=\"mw-mmv-source\"><span style=\"color: #000000\">In the case of 2-butanol (Fig 5.20), the first priority and the fourth priority are easy to assign.\u00a0 The -OH is first priority and the\u00a0-H is fourth priority.\u00a0 How do you assign 2nd and\u00a03rd priority, since both of those atoms are carbon?\u00a0 If the priority is the same for an attached atom, you need to look out to the next level and evaluate priority there.\u00a0 For 2-butanol,\u00a0one group is -CH<sub>3<\/sub> and one group is -CH<sub>2<\/sub>CH<sub>3<\/sub>.\u00a0 In the first situation, if we look out to the next level, this carbon is bound to three other\u00a0hydrogen atoms (all very low priority).\u00a0 In the second situation, the carbon is bound to two hydrogens and one\u00a0carbon.\u00a0 Since C has a higher priority than H, the -CH<sub>2<\/sub>CH<sub>3<\/sub> group will have higher priority over the -CH<sub>3<\/sub> group. \u00a0Once all of the groups have been assigned priority, you can determine which\u00a0direction the priority is moving. If it is\u00a0in the clockwise direction, the molecule is given the &#8216;R&#8217; designation. Priority moving in the counterclockwise direction is given the &#8216;S&#8217; designation. In our example, the 2-butanol on the left\u00a0shows priority moving in the counterclockwise direction giving the S-enantiomer. The molecule on the right shows the R-enantiomer with priority moving in the clockwise direction.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/stereochemistry-diagram-1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2352\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/stereochemistry-diagram-1-1024x555.png\" width=\"688\" height=\"373\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/stereochemistry-diagram-1.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/stereochemistry-diagram-1-300x163.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/stereochemistry-diagram-1-768x416.png 768w\" sizes=\"(max-width: 688px) 100vw, 688px\" \/><\/a><span><\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 5.20: Stereochemistry of 2-butanol.<\/strong> The CIP priority system can be used to determine the absolute stereo-conformation of enantiomers<\/span><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h4 id=\"thalidomide\"><span><strong>Thalidomide &#8211; A Story of Unintended Consequences<\/strong><\/span><\/h4>\n<p class=\"mw-mmv-source\"><span style=\"color: #000000\">Interestingly, enantiomers\u00a0have the same physical properties and exactly the same chemical properties, <em>except <\/em>when reacting with other chiral molecules. Thus, chiral molecules have potentially drastic differences in physiology and medicine. For example, in the 1960\u2019s, a drug called thalidomide was widely prescribed in\u00a0Western Europe\u00a0to alleviate morning sickness in pregnant women.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default aligncenter\" alt=\"image074.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4830\/image074.png?revision=1\" width=\"208\" height=\"145\" \/><\/p>\n<p><span style=\"color: #000000\">Thalidomide had previously been used in other countries as an antidepressant, and was believed to be safe and effective. It was not long, however, before doctors realized that something had gone horribly wrong: many babies born to women who had taken thalidomide during pregnancy suffered from severe birth defects.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal aligncenter\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/54216\/ThaNCP14053.jpg?revision=1\" width=\"417\" height=\"269\" \/><span style=\"color: #000000\"><strong>Figure 5.21: B<span class=\"mw-mmv-title\">aby born to a mother who had taken thalidomide while pregnant. <\/span><\/strong><em><span class=\"mw-mmv-title\">(<\/span><span class=\"mw-mmv-title\"><span class=\"credit\">OtisArchives3, CC BY 2.0) <\/span><\/span><\/em><strong><span class=\"mw-mmv-title\"><br \/>\n<\/span><\/strong><\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">Researchers later realized the that problem lay in the fact that thalidomide was being provided as a mixture of two different isomeric forms, called a <strong><em>racemic mixture<\/em><\/strong>.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default aligncenter\" alt=\"image076.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4832\/image076.png?revision=1&amp;size=bestfit&amp;width=487&amp;height=163\" width=\"487\" height=\"163\" \/><\/p>\n<p><span style=\"color: #000000\">One of the isomers is an effective medication, while\u00a0the other caused the side effects. Both isomeric forms have the same molecular formula and the same atom-to-atom connectivity, so they are not merely structural isomers.\u00a0 Where they differ is in the arrangement in three-dimensional space about one tetrahedral chiral carbon.\u00a0 Thus, these\u00a0two forms of thalidomide are <strong><em>enantiomers<\/em>.<\/strong><\/span><\/p>\n<p><span style=\"color: #000000\">Note that the carbon in question has <em>four different substituents<\/em> (two of these just happen to be connected by a ring structure). Tetrahedral carbons with four different substituent groups are called <em><strong>stereocenters<\/strong>.<\/em><\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-carbon-practice.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2128\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-carbon-practice-1024x638.png\" width=\"683\" height=\"426\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-carbon-practice-1024x638.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-carbon-practice-300x187.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-carbon-practice-768x478.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-carbon-practice.png 1045w\" sizes=\"(max-width: 683px) 100vw, 683px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Looking at the structures of what we are referring to as the two isomers of thalidomide, you may not be entirely convinced that they are actually two different molecules.\u00a0 In order to convince ourselves that they are indeed different, let\u2019s create a generalized picture of a tetrahedral carbon stereocenter, with the four substituents designated R<sub>1<\/sub>-R<sub>4<\/sub>.\u00a0 The two stereoisomers of our simplified model look like this:<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image080.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4836\/image080.png?revision=1&amp;size=bestfit&amp;width=243&amp;height=187\" width=\"243\" height=\"187\" \/><\/p>\n<p><span style=\"color: #000000\">If you look carefully at the figure above, you will notice that molecule A and molecule B are mirror images of each other (the line labeled &#8216;\u03c3&#8217; represents a mirror plane).\u00a0 Furthermore, <em>they are not superimposable<\/em>: if we pick up molecule A, flip it around, and place it next to molecule B, we see that the two structures cannot be superimposed on each other.\u00a0 They are two\u00a0different molecules!<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image082.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4838\/image082.png?revision=1&amp;size=bestfit&amp;width=217&amp;height=127\" width=\"217\" height=\"127\" \/><\/p>\n<p><span style=\"color: #000000\">If you make models of the two stereoisomers of thalidomide and do the same thing, you will see that they too are mirror images, and cannot be superimposed (it will help to look at a color version of the figure below).<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image084.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4840\/image084.png?revision=1&amp;size=bestfit&amp;width=479&amp;height=287\" width=\"479\" height=\"287\" \/><\/p>\n<p><span style=\"color: #000000\">Thalidomide is a <em>chiral<\/em> molecule.<\/span><\/p>\n<p><span style=\"color: #000000\">Here are some more examples of chiral molecules that exist as pairs of enantiomers.\u00a0 In each of these examples, there is a single stereocenter, indicated with an arrow.\u00a0 (Many molecules have more than one stereocenter, but we will get to that that a little later!)<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image086.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4842\/image086.png?revision=1&amp;size=bestfit&amp;width=674&amp;height=303\" width=\"652\" height=\"293\" \/><\/p>\n<p><span style=\"color: #000000\">Here are some examples of molecules that are <strong><em>achiral<\/em><\/strong> (not chiral). Notice that none of these molecules has a stereocenter (an atom\u00a0that is bound to four different substituents).<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image088.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4844\/image088.png?revision=1&amp;size=bestfit&amp;width=532&amp;height=353\" width=\"532\" height=\"353\" \/><\/p>\n<p><span style=\"color: #000000\">When evaluating a molecule for chirality, it is important to recognize that the use of the dashed\/solid wedge drawing does not necessarily mean that the molecule is chiral.\u00a0Chiral molecules are sometimes drawn without using wedges. Conversely, wedges may be used on carbons that are not stereocenters \u2013 look, for example, at the drawings of glycine and citrate in the figure above.\u00a0 Just because you see dashed and solid wedges in a structure, do not automatically assume that you are looking at a stereocenter.<\/span><\/p>\n<p><span style=\"color: #000000\">Other elements in addition to carbon can be stereocenters.\u00a0 The phosphorus center of phosphate ion and organic phosphate esters, for example, is tetrahedral, and thus is potentially a stereocenter.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image090.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4846\/image090.png?revision=1&amp;size=bestfit&amp;width=520&amp;height=125\" width=\"520\" height=\"125\" \/><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-achiral-practice-1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2134\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-achiral-practice-1-1024x692.png\" width=\"686\" height=\"463\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-achiral-practice-1-1024x692.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-achiral-practice-1-300x203.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-achiral-practice-1-768x519.png 768w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/chiral-achiral-practice-1.png 1048w\" sizes=\"(max-width: 686px) 100vw, 686px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\">Having trouble visualizing chirality and enantiomers?\u00a0 It may be helpful to watch this<\/span><\/p>\n<p><span><a title=\"https:\/\/www.khanacademy.org\/science\/organic-chemistry\/stereochemistry-topic\/chirality-r-s-system\/v\/introduction-to-chirality\" class=\"link-https\" href=\"https:\/\/www.khanacademy.org\/science\/organic-chemistry\/stereochemistry-topic\/chirality-r-s-system\/v\/introduction-to-chirality\" target=\"_blank\" rel=\"external nofollow noopener\">video tutorial<\/a><\/span><\/p>\n<h4><span><em><strong><a href=\"#CH103top5\"><span style=\"color: #ff0000\">(Back to the Top)<\/span><\/a><\/strong><\/em><\/span><\/h4>\n<hr \/>\n<h3 id=\"protein\"><span><strong>5.9 The Importance of Chirality in Protein Interactions<\/strong><\/span><\/h3>\n<p><span style=\"color: #000000\">The thalidomide that was used in the 1960s to treat depression and morning sickness was sold as a 50:50 mixture of both the R and the S enantiomer \u2013 this is referred to as a <strong>racemic mixture<\/strong>. A &#8216;squiggly&#8217; bond in a chemical structure indicates a racemic mixture &#8211; thus racemic (<em>R\/S<\/em>) thalidomide would be drawn as:<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image_108New.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/5029\/image_108New.png?revision=1&amp;size=bestfit&amp;width=279&amp;height=197\" width=\"279\" height=\"197\" \/><\/p>\n<p><span style=\"color: #000000\">The problem with racemic thalidomide, as we learned above,\u00a0is that only the R enantiomer\u00a0is an effective medicine, while the S enantiomer causes mutations in the developing fetus.\u00a0 How does such a seemingly trivial structural variation lead to such a dramatic (and in this case, tragic) difference in biological activity?\u00a0 Virtually all drugs work by interacting in some way with important proteins in our cells: they may bind to pain receptor proteins to block the transmission of pain signals, for instance, or clog up the active site of an enzyme that is involved in the synthesis of cholesterol.\u00a0 Proteins are chiral molecules, and are very sensitive to stereochemistry: just as a right-handed glove won&#8217;t fit on your left hand, a protein that is able to bind tightly to (<em>R<\/em>)-thalidomide may not bind well at all to (<em>S<\/em>)-thalidomide (it will help to view a color version of the figure below).<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image110.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4866\/image110.png?revision=1\" width=\"499\" height=\"212\" \/><\/p>\n<p><span style=\"color: #000000\">Instead, it seems that (<em>S<\/em>)-thalidomide interacts somehow with a protein involved in the development of a growing fetus, eventually causing the observed birth defects.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/receptor-interaction.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-2139\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/receptor-interaction.jpg\" width=\"680\" height=\"334\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/receptor-interaction.jpg 680w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/receptor-interaction-300x147.jpg 300w\" sizes=\"(max-width: 680px) 100vw, 680px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>\u00a0Figure 5.22 Drug binding sites on proteins are stereospecific.<\/strong><\/span><\/p>\n<p><span><span style=\"color: #000000\">Source: <\/span><a href=\"http:\/\/www.kshitij-iitjee.com\/Study\/Chemistry\/Part2\/Chapter3\/109.jpg\">www.kshitij-iitjee.com\/Study\/Chemistry\/Part2\/Chapter3\/109.jpg<\/a><\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">The over-the-counter painkiller ibuprofen is currently sold as a racemic mixture, but only the <em>S<\/em> enantiomer is effective.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image112.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4868\/image112.png?revision=1\" width=\"436\" height=\"150\" \/><\/p>\n<p><span style=\"color: #000000\">Fortunately, the <em>R<\/em> enantiomer does not produce any dangerous side effects, although its presence does seem to increase the amount of time that it takes for (<em>S<\/em>)-ibuprofen to take effect.<\/span><\/p>\n<p><span style=\"color: #000000\">You can, with the assistance your instructor, directly experience the biological importance of stereoisomerism. Carvone is a chiral, plant-derived molecule that smells like spearmint in the <em>R<\/em> form and caraway (a spice) in the <em>S<\/em> form.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"image114.png\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/4870\/image114.png?revision=1\" width=\"229\" height=\"168\" \/><\/p>\n<p><span style=\"color: #000000\">The two enantiomers interact differently with smell receptor proteins in your nose, generating the transmission of different chemical signals to the olfactory center of your brain.<\/span><\/p>\n<h4 style=\"text-align: left\"><a href=\"#CH103top5\"><span style=\"color: #ff0000\"><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/h4>\n<hr \/>\n<\/div>\n<h3 id=\"recog\"><span><strong>5.10 Common Organic Functional Groups<\/strong><\/span><\/h3>\n<p><span style=\"color: #000000\">The number of known organic compounds is a quite large. In fact, there are many times more organic compounds known than all the other (inorganic) compounds discovered so far, about 7 million organic compounds in total. Fortunately, organic chemicals consist of a relatively few similar parts, combined in different ways, that allow us to predict how a compound we have never seen before may react, by comparing how other molecules containing the same types of parts are known to react.<\/span><\/p>\n<\/div>\n<p><span style=\"color: #000000\">These parts of organic molecules are called <strong><em>functional groups<\/em><\/strong> and are made\u00a0up from\u00a0specific bonding\u00a0patterns with the\u00a0atoms most commonly\u00a0found in organic molecules (C, H, O, N, S, and P).\u00a0The identification of functional groups and the ability to predict reactivity based on functional group properties is one of the cornerstones of organic chemistry.<\/span><\/p>\n<p><span style=\"color: #000000\"><strong><em>Functional groups<\/em><\/strong> are specific atoms, ions, or groups of atoms having consistent properties. A functional group makes up part of a larger molecule.<\/span><\/p>\n<p><span style=\"color: #000000\">For example, -OH, the hydroxyl group that characterizes alcohols, is an oxygen with a hydrogen attached. It could be found on any number of different molecules.<\/span><\/p>\n<p><span style=\"color: #000000\">Just as elements have distinctive properties, functional groups have characteristic chemistries. An -OH functional group on one molecule will tend to react similarly, although perhaps not identically, to an -OH on another molecule.<\/span><\/p>\n<p><span style=\"color: #000000\">Organic reactions usually take place at the functional group, so learning about the reactivities of functional groups will prepare you to understand many other things about organic chemistry.<\/span><\/p>\n<p><span style=\"color: #000000\">Functional groups are structural units within organic compounds that are defined by specific bonding arrangements between specific atoms.\u00a0 The structure of capsaicin, the fiery compound found in hot peppers, incorporates several functional groups, labeled in the figure below and explained throughout this section.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63449\/fig1-2-1.png?revision=1\" width=\"497\" height=\"173\" \/><\/p>\n<p><span style=\"color: #000000\">As we progress in our study of organic chemistry, it will become extremely important to be able to quickly recognize the most common functional groups, because <em>they are the key structural elements that define how organic molecules react<\/em>.\u00a0 For now, we will only worry about drawing and recognizing each functional group, as depicted by Lewis and line structures.\u00a0 Much of the remainder of your study of organic chemistry will be taken up with learning about how the different functional groups behave in organic reactions. Below is a brief introduction to the major organic functional groups.<\/span><\/p>\n<h4><span style=\"color: #ff0000\"><a href=\"#CH103top5\" style=\"color: #ff0000\"><em><strong>(Back<\/strong><\/em><\/a><em><strong> to the Top)<\/strong><\/em><\/span><\/h4>\n<hr \/>\n<h4 id=\"alkanes\"><span><strong>Alkanes<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">The &#8216;default&#8217; in organic chemistry (essentially, the <em>lack<\/em> of any functional groups) is given the term <em><strong>alkane<\/strong><\/em>, characterized by single bonds between carbon and carbon, or between carbon and hydrogen.\u00a0 Methane, CH<sub>4<\/sub>, is the natural gas you may burn in your furnace.\u00a0 Octane, C<sub>8<\/sub>H<sub>18<\/sub>, is a component of gasoline.<\/span><\/p>\n<div>\n<div id=\"example\">\n<h4><span>\u00a0<\/span><\/h4>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63450\/fig1-2-2.png?revision=1\" width=\"522\" height=\"242\" \/><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<\/div>\n<\/div>\n<hr \/>\n<h4 id=\"alkenes\"><span><strong>Alkenes and Alkynes<\/strong><\/span><i><\/i><u><\/u><sub><\/sub><sup><\/sup><span><\/span><\/h4>\n<p><span style=\"color: #000000\"><strong><em>Alkenes<\/em> <\/strong>(sometimes called olefins) have carbon-carbon double bonds, and <strong><em>alkynes<\/em> <\/strong>have carbon-carbon triple bonds.\u00a0 Ethene, the simplest alkene example, is a gas that serves as a cellular signal in fruits to stimulate ripening.\u00a0 (If you want bananas to ripen quickly, put them in a paper bag along with an apple &#8211; the apple emits ethene gas (also called ethylene), setting off the ripening process in the bananas). Ethyne, commonly called acetylene, is used as a fuel in welding blow torches.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63452\/fig1-2-3.png?revision=1\" width=\"333\" height=\"168\" \/><\/p>\n<p><span style=\"color: #000000\">Many alkenes can take two geometric forms: <em>cis<\/em> or <em>trans<\/em>. The <em>cis<\/em> and <em>trans<\/em> forms of a given alkene are different\u00a0isomers with different physical properties because there is a very high energy barrier to rotation about a double bond. In the example below, the difference between <em>cis<\/em> and <em>trans<\/em> alkenes is readily apparent.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63453\/fig1-2-4.png?revision=1\" width=\"630\" height=\"273\" \/><\/p>\n<p><span style=\"color: #000000\">Alkanes, alkenes, and alkynes are all classified as <strong><em>hydrocarbons<\/em><\/strong>, because they are composed solely of carbon and hydrogen atoms. Alkanes are said to be <strong><em>saturated hydrocarbons<\/em><\/strong>, because the carbons are bonded to the maximum possible number of hydrogens\u00a0 &#8211; in other words, they are &#8216;<em>saturated&#8217;<\/em> with hydrogen atoms.\u00a0 The double and triple-bonded carbons in alkenes and alkynes have fewer hydrogen atoms bonded to them &#8211; they are thus referred to as <strong><em>unsaturated hydrocarbons<\/em><\/strong>.<br \/>\n<\/span><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h4 id=\"aromatics\"><span><strong>Aromatics<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">The <strong><em>aromatic group<\/em> <\/strong>is exemplified by benzene (which used to be a commonly used solvent on the organic lab, but which was shown to be carcinogenic), and naphthalene, a compound with a distinctive &#8216;mothball&#8217; smell. Aromatic groups are planar (flat) ring structures, and are widespread in nature.<\/span><\/p>\n<div>\n<div id=\"example\">\n<h4><span>\u00a0<\/span><\/h4>\n<div>\n<div>\n<p class=\"boxtitle\"><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63455\/fig1-2-5.png?revision=1\" width=\"528\" height=\"159\" \/><\/p>\n<p class=\"boxtitle\"><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h4 id=\"halides\"><span><strong>Alkyl Halides<\/strong><\/span><\/h4>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><span style=\"color: #000000\">When the carbon of an alkane is bonded to one or more halogens, the group is referred to as an <strong><em>alkyl halide or haloalkane<\/em><\/strong>.\u00a0 Chloroform is a useful solvent in the laboratory, and was one of the earlier anesthetic drugs used in surgery. Chlorodifluoromethane was used as a refrigerant and in aerosol sprays until the late twentieth century, but its use was discontinued after it was found to have harmful effects on the ozone layer. Bromoethane is a simple alkyl halide often used in organic synthesis. Alkyl halides groups are quite rare in biomolecules.<\/span><\/p>\n<div>\n<div>\n<div id=\"example\">\n<h4><span>\u00a0<\/span><\/h4>\n<div><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63456\/fig1-2-6.png?revision=1\" width=\"555\" height=\"169\" \/><\/div>\n<div><\/div>\n<div><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/div>\n<\/div>\n<\/div>\n<hr \/>\n<h4 id=\"alcohols\"><span><strong>Alcohols, Phenols, and Thiols<\/strong><\/span><\/h4>\n<div>\n<p><span style=\"color: #000000\">In the <em><strong>alcohol<\/strong><\/em> functional group, a carbon is single-bonded to an OH group (the OH group, when it is part of a larger molecule, is referred to as a <em><strong>hydroxyl group<\/strong><\/em>). Except for methanol, all alcohols can be classified as primary, secondary, or tertiary.\u00a0 In a primary alcohol, the carbon bonded to the OH group is also bonded to only one other carbon.\u00a0 In a secondary alcohol and tertiary alcohol, the carbon is bonded to two or three other carbons, respectively. When the hydroxyl group is <em>directly<\/em> attached to an aromatic ring, the resulting group is called a <strong><em>phenol.<\/em><\/strong> The sulfur analog of an alcohol is called a thiol (from the Greek <em>thio<\/em>, for sulfur).<\/span><\/p>\n<\/div>\n<div>\n<div>\n<div id=\"example\">\n<h4><b><\/b><\/h4>\n<div><\/div>\n<div><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63457\/fig1-2-7.png?revision=1\" width=\"658\" height=\"298\" \/><\/div>\n<div><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div><\/div>\n<p><span style=\"color: #000000\">Note that the definition of a phenol states that the hydroxyl oxygen must be <em>directly<\/em> attached to one of the carbons of the aromatic ring. The compound below, therefore, is <em>not<\/em> a phenol &#8211; it is a primary alcohol.<\/span><\/p>\n<\/div>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63458\/fig1-2-8.png?revision=1\" width=\"312\" height=\"240\" \/><\/p>\n<p><span style=\"color: #000000\">The distinction is important, because there is a significant difference in the reactivity of alcohols and phenols<\/span><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h4 id=\"ethers\"><span><strong>Ethers and Sulfides<i><\/i><u><\/u><sub><\/sub><sup><\/sup><\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">In an <strong><em>ether<\/em> <\/strong>functional group, an oxygen is bonded to two carbons. Below is the structure of diethyl ether, a common laboratory solvent and also one of the first compounds to be used as an anesthetic during operations. The sulfur analog of an ether is called a <em><strong>thioether or sulfide<\/strong><\/em>.<\/span><\/p>\n<div>\n<div id=\"example\">\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63461\/fig1-2-10.png?revision=1\" width=\"423\" height=\"221\" \/><\/p>\n<\/div>\n<\/div>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h4 id=\"amines\"><span><strong>Amines<i><\/i><u><\/u><sub><\/sub><sup><\/sup><\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\"><strong><em>Amines<\/em><\/strong> are characterized by nitrogen atoms with single bonds to hydrogen and carbon. Just as there are primary, secondary, and tertiary alcohols, there are primary, secondary, and tertiary amines. Ammonia is a special case with no carbon atoms.<\/span><\/p>\n<p><span style=\"color: #000000\">One of the most important properties of amines is that they are basic, and are readily protonated to form ammonium cations. In the case where a nitrogen has four bonds to carbon (which is somewhat unusual in biomolecules), it is called a quaternary ammonium ion.<\/span><\/p>\n<div>\n<div id=\"example\">\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63462\/fig1-2-11.png?revision=1\" width=\"682\" height=\"281\" \/><\/p>\n<\/div>\n<\/div>\n<div id=\"note\">\n<p><span style=\"color: #000000\">Note: Do not be confused by how the terms &#8216;primary&#8217;, &#8216;secondary&#8217;, and &#8216;tertiary&#8217; are applied to alcohols and amines &#8211; the definitions are different.\u00a0 In alcohols, what matters is how many other carbons the alcohol <em>carbon<\/em> is bonded to, while in amines, what matters is how many carbons the <em>nitrogen<\/em> is bonded to.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63463\/fig1-2-12.png?revision=1\" width=\"454\" height=\"188\" \/><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h4 id=\"phosphate\"><span><strong>Organic Phosphates<i><\/i><u><\/u><sub><\/sub><sup><\/sup><\/strong><\/span><\/h4>\n<\/div>\n<p><span style=\"color: #000000\">Phosphate and its derivative functional groups are ubiquitous in biomolecules.\u00a0 Phosphate linked to a single organic group is called a <em><strong>phosphate ester<\/strong><\/em>; when it has two links to organic groups it is called a phosphate diester.\u00a0 A linkage between two phosphates creates a phosphate anhydride.<\/span><\/p>\n<div>\n<div id=\"example\">\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63465\/fig1-2-13.png?revision=1\" width=\"674\" height=\"152\" \/><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<\/div>\n<\/div>\n<h4 id=\"aldehydes\"><strong><span>Aldehydes and\u00a0Ketones<\/span><\/strong><\/h4>\n<p><span style=\"color: #000000\">There are a number of functional groups that contain a carbon-oxygen double bond, which is commonly referred to as a <strong><em>carbonyl<\/em>.<\/strong>\u00a0\u00a0 Ketones and aldehydes are two closely related carbonyl-based functional groups that react in very similar ways.\u00a0 In a <strong><em>ketone<\/em><\/strong>, the carbon atom of a carbonyl is bonded to two other carbons.\u00a0 In an <em><strong>aldehyde,<\/strong><\/em> the carbonyl carbon is bonded on one side to a hydrogen, and on the other side to a carbon.\u00a0 The exception to this definition is formaldehyde, in which the carbonyl carbon has bonds to two hydrogens.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/aldehydes-and-ketones.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2143\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/aldehydes-and-ketones.png\" width=\"466\" height=\"134\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/aldehydes-and-ketones.png 783w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/aldehydes-and-ketones-300x86.png 300w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/aldehydes-and-ketones-768x221.png 768w\" sizes=\"(max-width: 466px) 100vw, 466px\" \/><\/a><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<div>\n<div id=\"example\">\n<div>\n<div id=\"example\">\n<div>\n<h4 id=\"carbox\"><span><strong>Carboxylic Acids and Their\u00a0Derivatives<\/strong><\/span><\/h4>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><span style=\"color: #000000\">When a carbonyl carbon is bonded on one side to a carbon (or hydrogen) and on the other side to an oxygen, nitrogen, or sulfur, the functional group is considered to be one of the \u2018carboxylic acid derivatives\u2019, a designation that describes a set of related functional groups.\u00a0 The\u00a0main member of this family is the <em><strong>carboxylic acid<\/strong><\/em> functional group, in which the carbonyl is bonded to a hydroxyl group.\u00a0\u00a0 The <strong><em>carboxylate ion\u00a0<\/em><\/strong>form has donated the H<sup>+<\/sup> to the solution.\u00a0 Other derivatives are <strong><em>carboxylic esters<\/em> <\/strong>(usually just called &#8216;esters&#8217;), <em><strong>thioesters, amides, acyl phosphates, acid chlorides<\/strong><\/em>, and <em><strong>acid anhydrides<\/strong><\/em>.\u00a0 With the exception of acid chlorides and acid anhydrides, the carboxylic acid derivatives are very common in biological molecules and\/or metabolic pathways and will be discussed in further details in a later chapter.<br \/>\n<\/span><\/p>\n<div>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63467\/fig1-2-15.png?revision=1\" width=\"681\" height=\"279\" \/><\/p>\n<p><a href=\"#CH103top5\"><span><em><strong>(Back to the Top)<\/strong><\/em><\/span><\/a><\/p>\n<div><\/div>\n<\/div>\n<div>\n<div id=\"example\">\n<hr \/>\n<\/div>\n<\/div>\n<h4 id=\"practicefunc\"><span><strong>Practice Recognizing Functional Groups in\u00a0Molecules<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">A single compound often contains several functional groups, particularly in biological organic chemistry.\u00a0 The six-carbon sugar molecules glucose and fructose, for example, contain aldehyde and ketone groups, respectively, and both contain five alcohol groups. A compound with several alcohol groups is often referred to as a <strong><em>\u2018polyol\u2019<\/em><\/strong>.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63519\/fig1-2-17.png?revision=1\" width=\"452\" height=\"170\" \/><\/p>\n<p><span style=\"color: #000000\">The hormone testosterone, the amino acid phenylalanine, and the glycolysis metabolite dihydroxyacetone phosphate all contain multiple functional groups, as labeled below.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63520\/fig1-2-18.png?revision=1\" width=\"592\" height=\"459\" \/><\/p>\n<p><span style=\"color: #000000\">While not in any way a complete list, this section has covered most of the important functional groups that we will encounter in biochemistry. Table\u00a05.7 provides a summary of all of the groups listed in this section. <\/span><\/p>\n<h4><span style=\"color: #000000\"><strong>Table 5.7 Common Organic Functional Groups<\/strong><\/span><\/h4>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/functional_groups_part_1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2359\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/functional_groups_part_1.png\" width=\"684\" height=\"586\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/functional_groups_part_1.png 737w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/functional_groups_part_1-300x257.png 300w\" sizes=\"(max-width: 684px) 100vw, 684px\" \/><\/a><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/functional_groups_part_2.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2360\" alt=\"\" src=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/functional_groups_part_2.png\" width=\"683\" height=\"646\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2017\/01\/functional_groups_part_2.png 740w, https:\/\/wou.edu\/chemistry\/files\/2017\/01\/functional_groups_part_2-300x284.png 300w\" sizes=\"(max-width: 683px) 100vw, 683px\" \/><\/a><\/p>\n<div>\n<div id=\"exercise\">\n<h4 class=\"boxtitle\"><strong><span>Exercise 5.10.1<\/span><\/strong><\/h4>\n<p><span style=\"color: #000000\">Identify the functional groups (other than alkanes) in the following organic compounds. State whether alcohols and amines are primary, secondary, or tertiary.<\/span><\/p>\n<p><span><img loading=\"lazy\" decoding=\"async\" class=\"internal default\" alt=\"\" src=\"http:\/\/chem.libretexts.org\/@api\/deki\/files\/63521\/figE1-2-1.png?revision=1\" width=\"575\" height=\"377\" \/><\/span><\/p>\n<h4 class=\"boxtitle\"><strong><span>Exercise 5.10.2<\/span><\/strong><\/h4>\n<p><span style=\"color: #000000\">Draw one example each of compounds fitting the descriptions below, using line structures.\u00a0 Be sure to designate the location of all non-zero formal charges. All atoms should have complete octets (phosphorus may exceed the octet rule). There are many possible correct answers for these, so be sure to check your structures with your instructor or tutor.<\/span><\/p>\n<p><span style=\"color: #000000\">a) a compound with molecular formula C<sub>6<\/sub>H<sub>11<\/sub>NO that includes alkene, secondary amine, and primary alcohol functional groups<\/span><\/p>\n<p><span style=\"color: #000000\">b) an ion with molecular formula C<sub>3<\/sub>H<sub>5<\/sub>O<sub>6<\/sub>P<sup>2-<\/sup> that\u00a0 includes aldehyde, secondary alcohol, and phosphate functional groups.<\/span><\/p>\n<p><span style=\"color: #000000\">c) A compound with molecular formula C<sub>6<\/sub>H<sub>9<\/sub>NO that has an amide functional group, and does <em>not<\/em> have an alkene group.<\/span><\/p>\n<h4><a href=\"#CH103top5\"><span style=\"color: #ff0000\"><strong><em>(back to the top)<\/em><\/strong><\/span><\/a><\/h4>\n<hr \/>\n<\/div>\n<\/div>\n<\/div>\n<h3 id=\"ch150-4.6\"><span><strong>5.11 Chapter Summary<\/strong><\/span><\/h3>\n<p class=\"para\" id=\"gob-ch04_s07_p02\"><span style=\"color: #000000\">Atoms can share pairs of valence electrons to obtain a valence shell octet. This sharing of electrons is a <strong class=\"emphasis bold\">covalent bond<\/strong>. A species formed from covalently bonded atoms is a <strong class=\"emphasis bold\">molecule<\/strong> and is represented by a <strong class=\"emphasis bold\">molecular formula<\/strong>, which gives the number of atoms of each type in the molecule. The two electrons shared in a covalent bond are called a <strong class=\"emphasis bold\">bonding pair of electrons<\/strong>. The electrons that do not participate in covalent bonds are called <strong class=\"emphasis bold\">nonbonding pairs<\/strong> (or <strong class=\"emphasis bold\">lone pairs<\/strong>) <strong class=\"emphasis bold\">of electrons<\/strong>. A covalent bond consisting of one pair of shared electrons is called a <strong class=\"emphasis bold\">single bond<\/strong>.<\/span><\/p>\n<p class=\"para\" id=\"gob-ch04_s07_p03\"><span style=\"color: #000000\">Covalent bonds occur between nonmetal atoms. Naming simple covalent compounds follows simple rules similar to those for ionic compounds. However, for covalent compounds, numerical prefixes are used as necessary to specify the number of atoms of each element in the compound.<\/span><\/p>\n<p class=\"para\" id=\"gob-ch04_s07_p04\"><span><span style=\"color: #000000\">In some cases, more than one pair of electrons is shared to satisfy the octet rule. Two pairs of electrons are shared by two atoms to make a <strong class=\"emphasis bold\">double bond<\/strong>. Three pairs of atoms are shared to make a <strong class=\"emphasis bold\">triple bond<\/strong>. Single, double, and triple covalent bonds may be represented by one, two, or three dashes, respectively, between the symbols of the atoms. In the case of a <strong>coordinate covalent bond<\/strong>, one atom supplies both of the electrons and the other atom does not supply any of the electrons.<\/span><br \/>\n<\/span><\/p>\n<p class=\"para\"><span style=\"color: #000000\">To judge the relative polarity of a covalent bond, chemists use <strong>electronegativity<\/strong>, which is a relative measure of how strongly an atom attracts electrons when it forms a covalent bond. The greater the electronegativity difference between the atoms involved in the covalent bond, the more polarity the bond displays.<br \/>\n<\/span><\/p>\n<p class=\"para\"><span style=\"color: #000000\">In comparison to ionic compounds, covalent molecules tend to have lower melting and boiling points, are less soluble in water, and are poor conductors of electricity. These major differences are largely due to increased polarity of ionic bonds when compared with covalent bonds.<\/span><\/p>\n<p><span style=\"color: #000000\">Organic molecules can be represented in a number of different ways.\u00a0 You should be able to recognize and draw out organic structures in each of these different structural representations: <strong>molecular formula, a displayed formula, a partially-condensed and fully-condensed structure, and line structures<\/strong> (with wedges and dashes when appropriate). In addition, regions of an organic structure may represented by an <strong>R-group<\/strong>, to save time in structure recreation. This is especially useful when drawing a group of related compounds that only differ in one or two regions. The differing regions of the molecule can be written out as R-groups to avoid having to redraw the entire molecule each time.<\/span><\/p>\n<p><span style=\"color: #000000\">Organic molecules can have isomer structures. <strong>Structural or constitutional isomers<\/strong> share the same molecular formula but the atoms within the structure are bonded together in a different orientation. <strong>Stereoisomers<\/strong> have the same molecular formula and the atoms are also bonded together in the same order, however, the 3-dimentional arrangement of the atoms in space is different. A special type of stereoisomer is called an enantiomer. <strong>Enantiomers<\/strong> are stereoisomers that are mirror images of eachother, but are not superimposable. Enantiomers have most of the same physical and chemical properties, however, since biological interactions depend on the 3-dimensional structure of molecules, enantiomers often have different biological activities. Molecules that are mirror images, but are not superimposable are said to have the property of <strong>chirality<\/strong> or handedness. Carbon displays chirality when it has four different substituents on it.<\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Functional groups<\/strong> are structural units within organic compounds that are defined by specific bonding arrangements between specific atoms. Just as elements have distinctive properties, functional groups have characteristic chemistries. An -OH functional group on one molecule will tend to react similarly, although not identically, to an -OH group on another molecule. Functional groups are the key structural elements that define how organic molecules react, thus it is important to learn how to recognize common organic functional groups.<\/span><\/p>\n<h4 class=\"mt-section\"><a href=\"#CH103top5\"><strong><em><span style=\"color: #ff0000\">(back to the top)<\/span><\/em><\/strong><\/a><\/h4>\n<hr \/>\n<h3 id=\"ch150-4.7\" class=\"mt-section\"><span><strong>5.12 References<\/strong><\/span><\/h3>\n<p><span style=\"color: #000000\">Chapter 5 materials have been adapted from the following creative commons resources unless otherwise noted:<\/span><\/p>\n<p><span style=\"color: #000000\">1. Organic Chemistry Portal. WikiUniversity. Available at:\u00a0<\/span> <a href=\"https:\/\/en.wikiversity.org\/wiki\/Portal:Organic_chemistry\">https:\/\/en.wikiversity.org\/wiki\/Portal:Organic_chemistry<\/a><\/p>\n<p><span><span style=\"color: #000000\">2. Anonymous. (2012) Introduction to Chemistry: General, Organic, and Biological (V1.0). Published under Creative Commons by-nc-sa 3.0. Available at<\/span>:<\/span> <a href=\"http:\/\/2012books.lardbucket.org\/books\/introduction-to-chemistry-general-organic-and-biological\/index.html\">http:\/\/2012books.lardbucket.org\/books\/introduction-to-chemistry-general-organic-and-biological\/index.html<\/a><\/p>\n<p><span style=\"color: #000000\">3. Poulsen, T. (2010) Introduction to Chemistry. Published under Creative Commons by-nc-sa 3.0. Available at:<\/span> <a href=\"http:\/\/openedgroup.org\/books\/Chemistry.pdf\">http:\/\/openedgroup.org\/books\/Chemistry.pdf<\/a><\/p>\n<p><span style=\"color: #000000\">4. Molecules and Molecular Compounds. (2017) Libretexts. Available at:<\/span> <a href=\"https:\/\/chem.libretexts.org\/Textbook_Maps\/General_Chemistry_Textbook_Maps\/Map%3A_Chemistry%3A_The_Central_Science_(Brown_et_al.)\/02._Atoms,_Molecules,_and_Ions\/2.6%3A_Molecules_and_Molecular_Compounds\">https:\/\/chem.libretexts.org\/Textbook_Maps\/General_Chemistry_Textbook_Maps\/Map%3A_Chemistry%3A_The_Central_Science_(Brown_et_al.)\/02._Atoms,_Molecules,_and_Ions\/2.6%3A_Molecules_and_Molecular_Compounds<\/a><\/p>\n<p><span style=\"color: #000000\">5. Clark, J. (2017) &#8216;General Principles of Chemical Bonding&#8217; Published by Libretexts. Available at:<\/span> <a href=\"https:\/\/chem.libretexts.org\/Core\/Physical_and_Theoretical_Chemistry\/Chemical_Bonding\/General_Principles_of_Chemical_Bonding\/Coordinate_(Dative_Covalent)_Bonding\">https:\/\/chem.libretexts.org\/Core\/Physical_and_Theoretical_Chemistry\/Chemical_Bonding\/General_Principles_of_Chemical_Bonding\/Coordinate_(Dative_Covalent)_Bonding<\/a><\/p>\n<p><span style=\"color: #000000\">6. OpenStax (2015) Atoms, Isotopes, Ions, and Molecules: The Building Blocks. OpenStax CNX.Available at:\u00a0<\/span> <a href=\"http:\/\/cnx.org\/contents\/be8818d0-2dba-4bf3-859a-737c25fb2c99@12\">http:\/\/cnx.org\/contents\/be8818d0-2dba-4bf3-859a-737c25fb2c99@12<\/a>.<\/p>\n<p><span style=\"color: #000000\">7.\u00a0 Wikipedia, Ionic Compound. Available at: <\/span><a href=\"https:\/\/en.wikipedia.org\/wiki\/Ionic_compound\">https:\/\/en.wikipedia.org\/wiki\/Ionic_compound<\/a><\/p>\n<p><span style=\"color: #000000\">8. Physical and Theoretical Chemistry (2017) Libretexts. Available at: <\/span><a href=\"https:\/\/chem.libretexts.org\/Core\/Physical_and_Theoretical_Chemistry\/Chemical_Bonding\/General_Principles_of_Chemical_Bonding\/Covalent_Bonds_vs_Ionic_Bonds\">https:\/\/chem.libretexts.org\/Core\/Physical_and_Theoretical_Chemistry\/Chemical_Bonding\/General_Principles_of_Chemical_Bonding\/Covalent_Bonds_vs_Ionic_Bonds<\/a>.<\/p>\n<p><span style=\"color: #000000\">9. Wikibooks. (2015)\u00a0Organic Chemistry. Available at:<\/span> <a href=\"https:\/\/en.wikibooks.org\/wiki\/Organic_Chemistry\">https:\/\/en.wikibooks.org\/wiki\/Organic_Chemistry<\/a>.<\/p>\n<p><span style=\"color: #000000\">10. Clark, J. (2014) How to Draw Organic Molecules. Available at:\u00a0<\/span> <a href=\"http:\/\/chem.libretexts.org\/Core\/Organic_Chemistry\/Fundamentals\/How_to_Draw_Organic_Molecules\">http:\/\/chem.libretexts.org\/Core\/Organic_Chemistry\/Fundamentals\/How_to_Draw_Organic_Molecules<\/a><\/p>\n<p><span style=\"color: #000000\">11.<a title=\"http:\/\/facultypages.morris.umn.edu\/~soderbt\/\" class=\"external\" href=\"http:\/\/facultypages.morris.umn.edu\/%7Esoderbt\/\" target=\"_blank\" rel=\"external nofollow noopener\" style=\"color: #000000\"> Soderberg, T. <\/a>(2016).<\/span> <span><a title=\"http:\/\/chemwiki.ucdavis.edu\/Organic_Chemistry\/Organic_Chemistry_With_a_Biological_Emphasis\" class=\"mt-self-link\" href=\"http:\/\/chem.libretexts.org\/Textbook_Maps\/Organic_Chemistry_Textbook_Maps\/Map%3A_Organic_Chemistry_With_a_Biological_Emphasis_%28Soderberg%29\" rel=\"internal\">Organic Chemistry With a Biological Emphasis . <\/a><span style=\"color: #000000\">Published under Creative Commons by-nc-sa 3.0.<\/span><a title=\"http:\/\/chemwiki.ucdavis.edu\/Organic_Chemistry\/Organic_Chemistry_With_a_Biological_Emphasis\" class=\"mt-self-link\" href=\"http:\/\/chem.libretexts.org\/Textbook_Maps\/Organic_Chemistry_Textbook_Maps\/Map%3A_Organic_Chemistry_With_a_Biological_Emphasis_%28Soderberg%29\" rel=\"internal\"><\/a><\/span><\/p>\n<p><span style=\"color: #000000\">12. Anonymous. (2012) Introduction to Chemistry: General, Organic, and Biological (V1.0). Published under Creative Commons by-nc-sa 3.0. Available at:<\/span> <a href=\"https:\/\/archive.org\/details\/fwk-archive-20121229-2547\">http:\/\/2012books.lardbucket.org\/books\/introduction-to-chemistry-general-organic-and-biological\/index.html<\/a><\/p>\n<p><span style=\"color: #000000\">13. Organic Chemistry Portal. WikiUniversity. Available at:<\/span>\u00a0 <a href=\"https:\/\/en.wikiversity.org\/wiki\/Portal:Organic_chemistry\">https:\/\/en.wikiversity.org\/wiki\/Portal:Organic_chemistry<\/a><\/p>\n<p><span style=\"color: #000000\">14. Anonymous. (2012) Introduction to Chemistry: General, Organic, and Biological (V1.0). Published under Creative Commons by-nc-sa 3.0. Available at:<\/span> <a href=\"https:\/\/archive.org\/details\/fwk-archive-20121229-2547\">http:\/\/2012books.lardbucket.org\/books\/introduction-to-chemistry-general-organic-and-biological\/index.html<\/a><\/p>\n<p><span style=\"color: #000000\">15. Poulsen, T. (2010) Introduction to Chemistry. Published under Creative Commons by-nc-sa 3.0. Available at:<\/span> <a href=\"http:\/\/openedgroup.org\/books\/Chemistry.pdf\">http:\/\/openedgroup.org\/books\/Chemistry.pdf<\/a><\/p>\n<p><span><span style=\"color: #000000\">16. OpenStax (2015) Atoms, Isotopes, Ions, and Molecules: The Building Blocks. OpenStax CNX.Available at:<\/span>\u00a0<\/span> <a href=\"http:\/\/cnx.org\/contents\/be8818d0-2dba-4bf3-859a-737c25fb2c99@12\">http:\/\/cnx.org\/contents\/be8818d0-2dba-4bf3-859a-737c25fb2c99@12<\/a>.<\/p>\n<p><span style=\"color: #000000\">17.\u00a0 Wikipedia, Ionic Compound. Available at:<\/span> <a href=\"https:\/\/en.wikipedia.org\/wiki\/Ionic_compound\">https:\/\/en.wikipedia.org\/wiki\/Ionic_compound<\/a><\/p>\n<h4><a href=\"#CH103top5\"><strong><em><span style=\"color: #ff0000\">(back to the top)<\/span><\/em><\/strong><\/a><\/h4>\n","protected":false},"excerpt":{"rendered":"<p>Chapter 5: Covalent Bonds and Introduction to Organic Molecules This text is published under creative commons licensing, for referencing and adaptation, please click here. \u00a05.1 Introduction to Covalent Molecules and Compounds How to Recognize Covalent Bonds 5.2 Electron Sharing Single Covalent Bonds Between the Same Atoms Single Covalent Bonds Between Different Atoms Multiple Covalent Bonds [&hellip;]<\/p>\n","protected":false},"author":280,"featured_media":0,"parent":4261,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_robots_primary_cat":"","_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","_lmt_disableupdate":"","_lmt_disable":"","_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-4291","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/pages\/4291","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/users\/280"}],"replies":[{"embeddable":true,"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/comments?post=4291"}],"version-history":[{"count":0,"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/pages\/4291\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/pages\/4261"}],"wp:attachment":[{"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/media?parent=4291"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}