{"id":3949,"date":"2018-08-16T14:49:42","date_gmt":"2018-08-16T21:49:42","guid":{"rendered":"http:\/\/www.wou.edu\/chemistry\/?page_id=3949"},"modified":"2023-05-12T13:47:38","modified_gmt":"2023-05-12T20:47:38","slug":"ch104-chapter-4-covalent-bonds-and-molecular-compounds","status":"publish","type":"page","link":"https:\/\/wou.edu\/chemistry\/courses\/online-chemistry-textbooks\/3890-2\/ch104-chapter-4-covalent-bonds-and-molecular-compounds\/","title":{"rendered":"CH104: Chapter 4 &#8211; Covalent Bonds and Molecular Compounds"},"content":{"rendered":"<h2 id=\"ch150top4\"><span><strong>Chapter 4 &#8211; Covalent Bonds and Molecular Compounds<\/strong><\/span><span><a href=\"https:\/\/wou.edu\/chemistry\/courses\/online-chemistry-textbooks\/ch105-consumer-chemistry\/\"><strong><em><\/em><\/strong><\/a><\/span><\/h2>\n<h3><a href=\"#ch150-4.1\"><span><strong>\u00a04.1<\/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>4.2 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>4.3 Electronegativity and Bond Polarity<\/strong><\/a><\/h3>\n<h3><a href=\"#ch150-4.4\"><strong>4.4 Properties of Molecular Compounds<\/strong><\/a><\/h3>\n<h3><a href=\"#ch150-4.5\"><span><strong>4.5 Naming Binary Molecular Compounds<\/strong><\/span><\/a><\/h3>\n<h3><span style=\"color: #ff0000\"><strong><a href=\"#lovecanal\">4.6 Focus on the Environment &#8211; The Love Canal<\/a><br \/>\n<\/strong><\/span><\/h3>\n<h3><a href=\"#ch150-4.6\"><span><strong>4.7 Chapter Summary<\/strong><\/span><\/a><\/h3>\n<h3><a href=\"#ch150-4.7\"><span><strong>4.8 References<\/strong><\/span><\/a><\/h3>\n<hr \/>\n<h2><span style=\"color: #000000\"><strong>Chapter 4 &#8211; Covalent Bonds and Molecular Compounds<\/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>\u00a04.1<\/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 <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\">4.1<\/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 4.1 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\u00a0predominantly\u00a0contain 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 CO<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 3<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 3, 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 4.2 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<hr \/>\n<h3 id=\"4.2sharing\"><span><strong>4.2 Electron Sharing<\/strong><\/span><\/h3>\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 3 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<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 4.3 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 4.3 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<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<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><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><\/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><em><span style=\"color: #000000\">The reaction between ammonia and hydrochloric acid<\/span><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-3949-1\" 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\"><span class=\"math\" id=\"MathJax-Span-1\"><span style=\"color: #000000\"><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><\/span><\/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 4.4 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<hr \/>\n<h3 id=\"ch150-4.3\"><strong>4.3 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 4.5. 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 4.5, is called a <em><strong>polar covalent bond<\/strong><\/em>. A covalent bond that has an equal sharing of electrons (part (a) of Figure 4.5) 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 4.5 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<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 4.6 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 4.6 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 4.7.<\/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 4.7 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 4.8) 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 4.8 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<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=\"#top4\"><span><em><strong>(BACK TO THE TOP)<\/strong><\/em><\/span><\/a><\/p>\n<hr \/>\n<h3 id=\"ch150-4.4\"><strong>4.4 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 4.1 shows common differences between covalent and ionic compounds.<\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Table 4.1 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>4.5 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 <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\">4.9<\/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><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 4.2 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 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\">.3<\/span><span class=\"mn\" id=\"MathJax-Span-164\">.<\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<p><span style=\"color: #000000\"><strong>Table 4.3 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<hr \/>\n<h3 id=\"lovecanal\"><strong>4.6 Focus on the Environment &#8211; The Love Canal<br \/>\n<\/strong><\/h3>\n<h4><span style=\"color: #c40e0e\"><strong>The Environmental Protection Agency<\/strong><\/span><\/h4>\n<p><span style=\"color: #000000\">On December 3rd of 1970 the United States Environmental Protection Agency (EPA) was proposed by President Richard Nixon to be an agency of the federal government charged with protecting human health and the environment. The agency was charged with writing and enforcing regulations based on laws passed by Congress.<\/span><\/p>\n<p><span style=\"color: #000000\">The main focus of the EPA as an agency is to conduct research, make environmental assessments, and provide educational materials for use by Congress and the American people regarding environmental and health concerns. The EPA also enforces national standards under a variety of environmental laws, such as the clean air act, and can levy fines, sanctions, and other measures on violators.\u00a0 Within this\u00a0 section, we will learn about creation of the Comprehensive Environmental Response, Compensation, and Liability Act, that is also known as <strong>&#8216;Superfund<\/strong>&#8216;. The Superfund program was instituted in 1980 and designed to identify and clean up the worst of the hazardous chemical waste sites in the U.S.\u00a0 The first of these sites was the Love Canal described in the next section.<\/span><\/p>\n<h4><span style=\"color: #c40e0e\"><strong>The Love Canal<\/strong><\/span><\/h4>\n<p id=\"x-ck12-YmVhMzhlNTI1OGZkNjEyZjczZTkzNzRjNDhkNzQ5OWQ.-183\"><span style=\"color: #000000\">One of the most famous and important examples of groundwater pollution in the U.S. is the <strong>Love Canal tragedy<\/strong> in Niagara Falls, New York (Figure 4.10). It is important because the pollution disaster at Love Canal, along with similar pollution calamities at that time (Times Beach, Missouri and Valley of Drums, Kentucky), helped to create\u00a0<strong>Superfund<\/strong>.<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Love-canal.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Love-canal-1024x943.png\" alt=\"\" class=\"alignnone wp-image-3959\" width=\"591\" height=\"544\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Love-canal-1024x943.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Love-canal-300x276.png 300w, https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Love-canal-768x707.png 768w, https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Love-canal.png 1085w\" sizes=\"(max-width: 591px) 100vw, 591px\" \/><\/a><\/p>\n<div class=\"wp-caption alignnone\">\n<p>&nbsp;<\/p>\n<p class=\"wp-caption-text\"><span style=\"color: #000000\"><strong>Figure 4.10. Love Canal. Source: US Environmental Protection Agency<\/strong><\/span><\/p>\n<hr \/>\n<\/div>\n<p id=\"x-ck12-MGNkOGFiZGY0ZjcyMmUzZTlmNjgwMTJhMzczMjQ1ZmE.-ykl\"><span style=\"color: #000000\">Love Canal is a neighborhood in Niagara Falls named after a large ditch (approximately 15 m wide, 3\u201312 m deep, and 1600 m long) that was dug in the 1890s for hydroelectric power. The ditch was abandoned before it actually generated any power and went mostly unused for decades, except for swimming by local residents. In the 1920s Niagara Falls began dumping urban waste into Love Canal, and in the 1940s the U.S. Army dumped waste from World War II there, including waste from the frantic effort to build a nuclear bomb. Hooker Chemical Company purchased the land in 1942 and lined it with clay. Then, the company put into Love Canal an estimated 21,000 tons of hazardous chemical waste, including the carcinogens benzene, dioxin, and polychlorobisphenols (PCBs) in large metal barrels and covered them with more clay (Figure 4.11).<\/span><\/p>\n<p><a href=\"https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Carcinogens.png\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Carcinogens-1024x575.png\" alt=\"\" class=\"alignnone wp-image-3956\" width=\"545\" height=\"306\" srcset=\"https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Carcinogens-1024x575.png 1024w, https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Carcinogens-300x168.png 300w, https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Carcinogens-768x431.png 768w, https:\/\/wou.edu\/chemistry\/files\/2018\/08\/Carcinogens.png 1660w\" sizes=\"(max-width: 545px) 100vw, 545px\" \/><\/a><\/p>\n<p><span style=\"color: #000000\"><strong>Figure 4.11 Examples of Carcinogens disposed of in the Love Canal.\u00a0<\/strong> (A) and (B) are representations of Benzene. In (A) all of the atoms in benzene are shown. (B) is a representative line structure of benzene where carbon atoms are indicated at every bend in every line and hydrogen atoms are implied. (C) line structure of dioxin, and (D) is a line diagram of a representative PCB.<\/span><\/p>\n<hr \/>\n<p><span style=\"color: #000000\">In 1953, Hooker sold the land to the Niagara Falls school board for $1, and included a clause in the sales contract that both described the land use (filled with chemical waste) and absolved them from any future damage claims from the buried waste. The school board promptly built a public school on the site and sold the surrounding land for a housing project that built 200 or so homes along the canal banks and another 1,000 in the neighborhood (Figure 4.10). During construction, the canal\u2019s clay cap and walls were breached, damaging some of the metal barrels.<\/span><\/p>\n<div id=\"x-ck12-M2JkMjMzYmEzNzIzZTY3ZjhjY2U3MjQ0ZjEyMTcyZTU.-nqw\" class=\"x-ck12-img-postcard x-ck12-nofloat\">\n<p id=\"x-ck12-NjIwZjVhYTA2NGJjYzk4ZjVlYzU3ZGJjNGYwYmQ4MzY.-jrn\" class=\"indent\"><span style=\"color: #000000\">Eventually, the chemical waste seeped into people\u2019s basements, and the metal barrels worked their way to the surface. Trees and gardens began to die; bicycle tires and the rubber soles of children\u2019s shoes disintegrated in noxious puddles. From the 1950s to the late 1970s, residents repeatedly complained of strange odors and substances that surfaced in their yards.\u00a0 Eckardt Beck, the EPA administrator for the region from 1977-1979 recalled in the EPA Journal, &#8220;I visited the canal area at that time.\u00a0 Corroding waste-disposal drums could be seen breaking up trough the grounds of backyards. Trees and gardens were turning black and dying. One entire swimming pool had been popped up from its foundation, afloat now on a small sea of chemicals. Puddles of noxious substances were pointed out to be by the residents. Some of these puddles were in their yards, some were in their basements, others yet on the school grounds.\u00a0 Everywhere the air had a faint, choking smell. Children returned from play with burns on their hands and faces. And then there were the birth defects. The New York State Health Department is continuing an investigation into a disturbingly high rate of miscarriages, along with five birth-defect cases detected thus far in the area.&#8221;<sup>10<\/sup><\/span><\/p>\n<p class=\"indent\"><span style=\"color: #000000\">In 1978 President Carter declared a state of emergency at Love Canal, making it the first human-caused environmental problem to be designated that way. The Love Canal incident became a symbol of improperly stored chemical waste. Clean up of Love Canal, which was funded by Superfund and completely finished in 2004, involved removing contaminated soil, installing drainage pipes to capture contaminated groundwater for treatment, and covering it with clay and plastic. In 1995, Occidental Chemical (the modern name for Hooker Chemical) paid $102 million to Superfund for cleanup and $27 million to Federal Emergency Management Association for the relocation of more than 1,000 families. New York State paid $98 million to EPA and the US government paid $8 million for pollution by the Army. The total clean up cost was estimated to be $275 million.<\/span><\/p>\n<\/div>\n<p id=\"x-ck12-ODc1ZmU2ZWYxZThmMTIyZDY0MjFiNWM2ZjVmZWIxMWE.-5f2\" class=\"indent\"><span style=\"color: #000000\">The Love Canal tragedy helped to create Superfund, which has analyzed tens of thousands of hazardous waste sites in the U.S. and cleaned up hundreds of the worst ones. Nevertheless, over 1,000 major hazardous waste sites with a significant risk to human health or the environment are still in the process of being cleaned.<\/span><\/p>\n<h5><span style=\"color: #000000\">Suggested Assignment:<\/span><\/h5>\n<p><span style=\"color: #000000\">1. Explore the <a href=\"https:\/\/www.epa.gov\/superfund\" style=\"color: #000000\"><span style=\"color: #ff0000\">EPA Superfund Website.<\/span><\/a><\/span><\/p>\n<p><span style=\"color: #000000\">2. Scroll down to the bottom of the page and select &#8216;Sites Where You Live&#8217;<\/span><\/p>\n<p><span style=\"color: #000000\">3.\u00a0 Select &#8216;Your State&#8217; and Show &#8216;All Sites&#8217;.<\/span><\/p>\n<p><span style=\"color: #000000\">4. Select a Superfund site within your state and write a 500 word summary describing your chosen site. In the first paragraph, describe the type of toxic waste that is found at the site and what the health and environmental impacts are due to the pollution. In a second paragraphs, describe who is responsible for generating the pollution and what has or is currently being done to restore and clean up the site. Be sure to include the monetary cost of the clean up in your response if it is disclosed and what parties are paying for the clean up.<\/span><\/p>\n<h3 id=\"ch150-4.6\"><span><strong>4.7 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 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.<br \/>\n<\/span><\/p>\n<p class=\"para\"><span><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.<\/span><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<h3 class=\"mt-section\"><\/h3>\n<hr \/>\n<h3 id=\"ch150-4.7\" class=\"mt-section\"><span><strong>4.8 References<\/strong><\/span><\/h3>\n<p><span style=\"color: #000000\">Chapter 4 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 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> <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. Lois Gibbs. (1998) Love Canal the story continues. Published by the Center for Health, Environment and Justice.\u00a0 Available at:<\/span>\u00a0<a href=\"http:\/\/chej.org\/wp-content\/uploads\/Love-Canal-PDF-v1.pdf\">http:\/\/chej.org\/wp-content\/uploads\/Love-Canal-PDF-v1.pdf<\/a><\/p>\n<p><span style=\"color: #000000\">10. Beck, E.C. (1979) The Love Canal Tragedy. EPA Journal. Available at:<\/span> <a href=\"https:\/\/archive.epa.gov\/epa\/aboutepa\/love-canal-tragedy.html\">https:\/\/archive.epa.gov\/epa\/aboutepa\/love-canal-tragedy.html<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Chapter 4 &#8211; Covalent Bonds and Molecular Compounds \u00a04.1 Introduction to Covalent Molecules and Compounds How to Recognize Covalent Bonds 4.2 Electron Sharing Single Covalent Bonds Between the Same Atoms Single Covalent Bonds Between Different Atoms Multiple Covalent Bonds Coordinate Covalent Bonds 4.3 Electronegativity and Bond Polarity 4.4 Properties of Molecular Compounds 4.5 Naming Binary [&hellip;]<\/p>\n","protected":false},"author":280,"featured_media":0,"parent":3890,"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":"no","_lmt_disable":"","_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-3949","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/pages\/3949","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=3949"}],"version-history":[{"count":0,"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/pages\/3949\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/pages\/3890"}],"wp:attachment":[{"href":"https:\/\/wou.edu\/chemistry\/wp-json\/wp\/v2\/media?parent=3949"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}