{"id":3098,"date":"2018-06-22T14:05:56","date_gmt":"2018-06-22T14:05:56","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/chapter\/3-1-two-types-of-bonding\/"},"modified":"2018-08-04T21:46:43","modified_gmt":"2018-08-04T21:46:43","slug":"1-3-basics-of-bonding","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/chapter\/1-3-basics-of-bonding\/","title":{"raw":"1.3. Basics of bonding","rendered":"1.3. Basics of bonding"},"content":{"raw":"<div>\r\n<div class=\"section\" xml:lang=\"en\">\r\n<h2 id=\"gob-ch03_s01_p01\" class=\"para editable block\"><a id=\"1.3.1.\"><\/a>1.3.1. How and why atoms bond<\/h2>\r\n<div id=\"navbar-top\" class=\"navbar\">\r\n<div class=\"navbar-part left\">\r\n<div class=\"textbox learning-objectives\">\r\n<h3>Learning Objectives<\/h3>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch03_s01\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch03_s01_n01\" class=\"learning_objectives editable block\">\r\n<ol id=\"gob-ch03_s01_l01\" class=\"orderedlist\">\r\n \t<li>Define the octet rule.<\/li>\r\n \t<li>Describe how ionic bonds are formed.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<p class=\"para editable block\">Atoms can join together by forming a <strong><span class=\"margin_term\"><span class=\"glossterm\">chemical bond<\/span><\/span>,<\/strong> which is a very strong attraction between two atoms. Chemical bonds are formed when electrons in different atoms interact with each other to make an arrangement that is more stable than when the atoms are apart.<\/p>\r\n<p id=\"gob-ch03_s01_p02\" class=\"para editable block\">What causes atoms to make a chemical bond with other atoms, rather than remaining as individual atoms? A clue comes by considering the noble gas elements, the rightmost column of the periodic table. These elements\u2014helium, neon, argon, krypton, xenon, and radon\u2014do not form compounds very easily, which suggests that they are especially stable as lone atoms. What else do the noble gas elements have in common? Except for helium, they all have eight valence electrons. Chemists have concluded that atoms are especially stable if they have eight electrons in their outermost shell. This useful rule of thumb is called the <strong><span class=\"margin_term\"><span class=\"glossterm\">octet rule<\/span><\/span><\/strong>, and it is a key to understanding why compounds form.<\/p>\r\n<p id=\"gob-ch03_s01_p04\" class=\"para editable block\">There are two ways for an atom that does not have an octet of valence electrons to obtain an octet in its outer shell. One way is the transfer of electrons between two atoms until all atoms have octets. Because some atoms will lose electrons and some atoms will gain electrons, there is no overall change in the number of electrons, but individual atoms acquire a nonzero electric charge. Those that lose electrons become positively charged, and those that gain electrons become negatively charged. Charged atoms are called <strong><span class=\"margin_term\"><span class=\"glossterm\">ions<\/span><\/span><\/strong>. Because opposite charges attract (while like charges repel), these oppositely charged ions attract each other, forming <strong><span class=\"margin_term\"><span class=\"glossterm\">ionic bonds<\/span><\/span>.<\/strong> The resulting compounds are called<strong> <span class=\"margin_term\"><span class=\"glossterm\">ionic compounds<\/span><\/span><\/strong>\u00a0and are the primary subject of this chapter.<\/p>\r\n<p id=\"gob-ch03_s01_p05\" class=\"para editable block\">The second way for an atom to obtain an octet of electrons is by sharing electrons with another atom. These shared electrons simultaneously occupy the outermost shell of more than one atom. The bond made by electron sharing is called a <strong class=\"emphasis bold\">covalent bond<\/strong>. Covalent bonding and covalent compounds will be discussed in detail below.<\/p>\r\n\r\n<div id=\"gob-ch03_s01_n03\" class=\"callout editable block\">\r\n<div class=\"textbox\">\r\n<p id=\"gob-ch03_s01_p06\" class=\"para\">NOTE: Despite our focus on the octet rule, we must remember that for small atoms, such as hydrogen, helium, and lithium, the first shell is, or becomes, the outermost shell and hold only two electrons. Therefore, these atoms satisfy a \u201cduet rule\u201d rather than the octet rule.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch03_s01_qs03\" class=\"qandaset block\">\r\n<div class=\"navbar\">\r\n<h2 class=\"navbar-part left\">1.3.2. Characteristics of covalent bonds<\/h2>\r\n<\/div>\r\n<div>\r\n<div id=\"gob-ch04_s04\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch04_s04_n01\" class=\"learning_objectives editable block\">\r\n<div class=\"textbox learning-objectives\">\r\n<h3 class=\"title\">Learning Objective<\/h3>\r\n<ol id=\"gob-ch04_s04_l01\" class=\"orderedlist\">\r\n \t<li>Compare covalent bonds in terms of bond length and bond polarity.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<p id=\"gob-ch04_s04_p01\" class=\"para editable block\">Covalent bonds have certain characteristics that depend on the identities of the atoms participating in the bond. Two characteristics are bond length and bond polarity.<\/p>\r\n\r\n<div id=\"gob-ch04_s04_s01\" class=\"section\">\r\n<h3 class=\"title editable block\">Bond length<\/h3>\r\n<p id=\"gob-ch04_s04_s01_p01\" class=\"para editable block\">The covalent bond in the hydrogen molecule (H<sub class=\"subscript\">2<\/sub>) has a certain length (about 7.4 \u00d7 10<sup class=\"superscript\">\u221211<\/sup> m). Other covalent bonds also have known bond lengths, which are dependent on both the identities of the atoms in the bond and whether the bonds are single, double, or triple bonds. <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1.<\/a> lists the approximate bond lengths for some single covalent bonds. The exact bond length may vary depending on the identity of the molecule but will be close to the value given in the table.<\/p>\r\n\r\n<div id=\"gob-ch04_s04_s01_t01\" class=\"table block\">\r\n<h4 class=\"title\"><strong><span class=\"title-prefix\">Table 1.1.<\/span> Approximate bond lengths of some single bonds<\/strong><\/h4>\r\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\r\n<thead>\r\n<tr>\r\n<th>Bond<\/th>\r\n<th align=\"right\">Length (\u00d7 10<sup class=\"superscript\">\u221212<\/sup> m)<\/th>\r\n<\/tr>\r\n<\/thead>\r\n<tbody>\r\n<tr>\r\n<td>H\u2013H<\/td>\r\n<td align=\"right\">74<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>H\u2013C<\/td>\r\n<td align=\"right\">110<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>H\u2013N<\/td>\r\n<td align=\"right\">100<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>H\u2013O<\/td>\r\n<td align=\"right\">97<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>H\u2013I<\/td>\r\n<td align=\"right\">161<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C\u2013C<\/td>\r\n<td align=\"right\">154<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C\u2013N<\/td>\r\n<td align=\"right\">147<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C\u2013O<\/td>\r\n<td align=\"right\">143<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N\u2013N<\/td>\r\n<td align=\"right\">145<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>O\u2013O<\/td>\r\n<td align=\"right\">145<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<\/div>\r\n<p id=\"gob-ch04_s04_s01_p02\" class=\"para editable block\"><a class=\"xref\" href=\"#gob-ch04_s04_s01_t02\">Table 1.2.<\/a> compares the lengths of single covalent bonds with those of double and triple bonds between the same atoms. Without exception, as the number of covalent bonds between two atoms increases, the bond length decreases. With more electrons between the two nuclei, the nuclei can get closer together before the internuclear repulsion is strong enough to balance the attraction.<\/p>\r\n\r\n<div id=\"gob-ch04_s04_s01_t02\" class=\"table block\">\r\n<h4 class=\"title\"><strong><span class=\"title-prefix\">Table 1.2.<\/span> Comparison of bond lengths for single and multiple bonds<\/strong><\/h4>\r\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\r\n<thead>\r\n<tr>\r\n<th>Bond<\/th>\r\n<th align=\"right\">Length (\u00d7 10<sup class=\"superscript\">\u221212<\/sup> m)<\/th>\r\n<\/tr>\r\n<\/thead>\r\n<tbody>\r\n<tr>\r\n<td>C\u2013C<\/td>\r\n<td align=\"right\">154<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C=C<\/td>\r\n<td align=\"right\">134<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C\u2261C<\/td>\r\n<td align=\"right\">120<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C\u2013N<\/td>\r\n<td align=\"right\">147<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C=N<\/td>\r\n<td align=\"right\">128<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C\u2261N<\/td>\r\n<td align=\"right\">116<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C\u2013O<\/td>\r\n<td align=\"right\">143<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C=O<\/td>\r\n<td align=\"right\">120<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>C\u2261O<\/td>\r\n<td align=\"right\">113<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N\u2013N<\/td>\r\n<td align=\"right\">145<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N=N<\/td>\r\n<td align=\"right\">123<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N\u2261N<\/td>\r\n<td align=\"right\">110<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>O\u2013O<\/td>\r\n<td align=\"right\">145<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>O=O<\/td>\r\n<td align=\"right\">121<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch04_s04_s02\" class=\"section\">\r\n<h3 class=\"title editable block\">Electronegativity and bond polarity<\/h3>\r\n[caption id=\"\" align=\"alignright\" width=\"273\"]<img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3369\/2018\/06\/22140559\/a63736e6eabf6300d625e2438ddfeaa7.jpg\" alt=\"image\" width=\"273\" height=\"468\" \/> <em>Figure 1.6. Polar versus nonpolar covalent bonds. <\/em>(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.[\/caption]\r\n<p id=\"gob-ch04_s04_s02_p01\" class=\"para editable block\">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 <a class=\"xref\" href=\"#gob-ch04_s04_s02_f01\">Figure 1.6. \"Polar versus Nonpolar Covalent Bonds\"<\/a>. 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 <a class=\"xref\" href=\"#gob-ch04_s04_s02_f01\">Figure 1.6.<\/a>, is called a <span class=\"margin_term\"><span class=\"glossterm\"><strong>polar covalent bond<\/strong>. <\/span><\/span>A covalent bond that has an equal sharing of electrons (part (a) is called a <span class=\"margin_term\"><span class=\"glossterm\"><strong>nonpolar covalent bond<\/strong>.<\/span><\/span><\/p>\r\n<p id=\"gob-ch04_s04_s02_p02\" class=\"para editable block\">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 rather than shared. To judge the relative polarity of a covalent bond, chemists use <strong><span class=\"margin_term\"><span class=\"glossterm\">electronegativity<\/span><\/span>,<\/strong> which is a relative measure of how strongly an atom attracts electrons when it forms a covalent bond. There are various numerical scales for rating electronegativity. <a class=\"xref\" href=\"#gob-ch04_s04_s02_f02\">Figure 1.7. \"Electronegativities of Various Elements\"<\/a> shows one of the most popular\u2014the Pauling scale. The polarity of a covalent bond can be judged by determining the difference in the electronegativities of the two atoms making the bond. The greater the difference in electronegativities, the greater the imbalance of electron sharing in the bond. Although there are no hard and fast rules, the general rule is if the difference in electronegativities is less than about 0.4, the bond is considered nonpolar; if the difference is greater than 0.4, the bond is considered polar. If 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.<\/p>\r\nWhen a molecule\u2019s bonds are polar, the substance is usually found to be 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.)\u00a0 This aspect will be discussed in more detail in <a href=\"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/chapter\/1-8-intermolecular-forces\/\">section 1.8. on intermolecular forces<\/a>.\r\n<div id=\"gob-ch04_s04_s02_f02\" class=\"figure large editable block\">\r\n\r\n[caption id=\"\" align=\"alignnone\" width=\"1538\"]<img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3369\/2018\/06\/22140603\/0b3884eacaf2db8be97ff0dc7ccaaae1.jpg\" alt=\"image\" width=\"1538\" height=\"996\" \/> <em>Figure 1.7. Electronegativities of Various Elements.\u00a0<\/em>A popular scale for electronegativities has the value for fluorine atoms set at 4.0, the highest value.[\/caption]\r\n<p class=\"para\"><\/p>\r\n\r\n<\/div>\r\n<div id=\"gob-ch04_s04_s02_n01\" class=\"callout block\">\r\n<div class=\"textbox shaded\">\r\n<h3 class=\"title\">Looking Closer: Linus Pauling<\/h3>\r\n<p id=\"gob-ch04_s04_s02_p03\" class=\"para\">Arguably the most influential chemist of the 20th century, Linus Pauling (1901\u201394) is the only person to have won two individual (that is, unshared) Nobel Prizes. In the 1930s, Pauling used new mathematical theories to enunciate some fundamental principles of the chemical bond. His 1939 book <em class=\"emphasis\">The Nature of the Chemical Bond<\/em> is one of the most significant books ever published in chemistry.<\/p>\r\n<p id=\"gob-ch04_s04_s02_p04\" class=\"para\">By 1935, Pauling\u2019s interest turned to biological molecules, and he was awarded the 1954 Nobel Prize in Chemistry for his work on protein structure. (He was very close to discovering the double helix structure of DNA when James Watson and James Crick announced their own discovery of its structure in 1953.) He was later awarded the 1962 Nobel Peace Prize for his efforts to ban the testing of nuclear weapons.<\/p>\r\n<p id=\"gob-ch04_s04_s02_p05\" class=\"para\">In his later years, Pauling became convinced that large doses of vitamin C would prevent disease, including the common cold. Most clinical research failed to show a connection, but Pauling continued to take large doses daily. He died in 1994, having spent a lifetime establishing a scientific legacy that few will ever equal.<\/p>\r\n\r\n<div class=\"informalfigure medium\">\r\n\r\n[caption id=\"\" align=\"alignright\" width=\"187\"]<img class=\"\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3369\/2018\/06\/22140606\/df9a49acad271a13b8e3a5fd85e30b33.jpg\" alt=\"image\" width=\"187\" height=\"288\" \/> <em>Linus Pauling was one of the most influential chemists of the 20th century.<\/em>[\/caption]\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch04_s04_s02_n02\" class=\"exercises editable block\">\r\n<h3 class=\"title\">Example 2<\/h3>\r\n<p id=\"gob-ch04_s04_s02_p06\" class=\"para\">Describe the electronegativity difference between each pair of atoms and the resulting polarity (or bond type).<\/p>\r\n\r\n<ol id=\"gob-ch04_s04_s02_l01\" class=\"orderedlist\">\r\n \t<li>C and H<\/li>\r\n \t<li>H and H<\/li>\r\n \t<li>Na and Cl<\/li>\r\n \t<li>O and H<\/li>\r\n<\/ol>\r\n<p class=\"simpara\">Solution<\/p>\r\n[reveal-answer q=\"979132\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"979132\"]\r\n<ol>\r\n \t<li>Carbon has an electronegativity of 2.5, while the value for hydrogen is 2.1. The difference is 0.3, which is rather small. The C\u2013H bond is therefore considered nonpolar.<\/li>\r\n \t<li>Both hydrogen atoms have the same electronegativity value\u20142.1. The difference is zero, so the bond is nonpolar.<\/li>\r\n \t<li>Sodium\u2019s electronegativity is 0.9, while chlorine\u2019s is 3.0. The difference is 2.1, which is rather high, and so sodium and chlorine form an ionic compound.<\/li>\r\n \t<li>With 2.1 for hydrogen and 3.5 for oxygen, the electronegativity difference is 1.4. We would expect a very polar bond, but not so polar that the O\u2013H bond is considered ionic.[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch04_s04_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox shaded\">\r\n<h3 class=\"title\">Skill-Building Exercise<\/h3>\r\n<ol id=\"gob-ch04_s04_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch04_s04_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs01_p02\" class=\"para\">C and O<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs01_p04\" class=\"para\">K and Br<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs01_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs01_p06\" class=\"para\">N and N<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs01_qd01_qa04\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs01_p08\" class=\"para\">Cs and F<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch04_s04_qs02\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<ol id=\"gob-ch04_s04_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch04_s04_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs02_p01\" class=\"para\">What is the name for the distance between two atoms in a covalent bond?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs02_p03\" class=\"para\">What does the electronegativity of an atom indicate?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs02_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs02_p05\" class=\"para\">What type of bond is formed between two atoms if the difference in electronegativities is small? Medium? Large?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox exercises\">\r\n<div class=\"qandaset block\">\r\n<h3 class=\"title\">Answers<\/h3>\r\n[reveal-answer q=\"557987\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"557987\"]\r\n<ol>\r\n \t<li>bond length<\/li>\r\n \t<li>Electronegativity is a qualitative measure of how much an atom attracts electrons in a covalent bond.<\/li>\r\n \t<li>nonpolar; polar; ionic[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch04_s04_s02_n05\" class=\"key_takeaways editable block\">\r\n<div class=\"textbox key-takeaways\">\r\n<h3 class=\"title\">Key Takeaways<\/h3>\r\n<ul id=\"gob-ch04_s04_s02_l05\" class=\"itemizedlist\">\r\n \t<li>Covalent bonds between different atoms have different bond lengths.<\/li>\r\n \t<li>Covalent bonds can be polar or nonpolar, depending on the electronegativity difference between the atoms involved.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch04_s04_qs03\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<h3>Exercises<\/h3>\r\n<ol id=\"gob-ch04_s04_qs03_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p01\" class=\"para\">Which is longer\u2014a C\u2013H bond or a C\u2013O bond? (Refer to <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1. \"Approximate Bond Lengths of Some Single Bonds\"<\/a>.)<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p03\" class=\"para\">Which is shorter\u2014an N\u2013H bond or a C\u2013H bond? (Refer to <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1. \"Approximate Bond Lengths of Some Single Bonds\"<\/a>.)<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p05\" class=\"para\">A nanometer is 10<sup class=\"superscript\">\u22129<\/sup> m. Using the data in <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1. \"Approximate Bond Lengths of Some Single Bonds\"<\/a> and <a class=\"xref\" href=\"#gob-ch04_s04_s01_t02\">Table 1.2. \"Comparison of Bond Lengths for Single and Multiple Bonds\"<\/a>, determine the length of each bond in nanometers.<\/p>\r\n\r\n<ol id=\"gob-ch04_s04_qs03_l01\" class=\"orderedlist\">\r\n \t<li>a C\u2013O bond<\/li>\r\n \t<li>a C=O bond<\/li>\r\n \t<li>an H\u2013N bond<\/li>\r\n \t<li>a C\u2261N bond<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa04\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p06\" class=\"para\">An angstrom (\u00c5) is defined as 10<sup class=\"superscript\">\u221210<\/sup> m. Using <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1. \"Approximate Bond Lengths of Some Single Bonds\"<\/a> and <a class=\"xref\" href=\"#gob-ch04_s04_s01_t02\">Table 1.2. \"Comparison of Bond Lengths for Single and Multiple Bonds\"<\/a>, determine the length of each bond in angstroms.<\/p>\r\n\r\n<ol id=\"gob-ch04_s04_qs03_l03\" class=\"orderedlist\">\r\n \t<li>a C\u2013C bond<\/li>\r\n \t<li>a C=C bond<\/li>\r\n \t<li>an N\u2261N bond<\/li>\r\n \t<li>an H\u2013O bond<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa05\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p07\" class=\"para\">Refer to Exercise 3. Why is the nanometer unit useful as a unit for expressing bond lengths?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa06\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p09\" class=\"para\">Refer to Exercise 4. Why is the angstrom unit useful as a unit for expressing bond lengths?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa07\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p11\" class=\"para\">Using <a class=\"xref\" href=\"#gob-ch04_s04_s02_f02\">Figure 1.7. \"Electronegativities of Various Elements\"<\/a>, determine which atom in each pair has the higher electronegativity.<\/p>\r\n\r\n<ol id=\"gob-ch04_s04_qs03_l05\" class=\"orderedlist\">\r\n \t<li>H or C<\/li>\r\n \t<li>O or Br<\/li>\r\n \t<li>Na or Rb<\/li>\r\n \t<li>I or Cl<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa08\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p12\" class=\"para\">Using <a class=\"xref\" href=\"#gob-ch04_s04_s02_f02\">Figure 1.7. \"Electronegativities of Various Elements\"<\/a>, determine which atom in each pair has the lower electronegativity.<\/p>\r\n\r\n<ol id=\"gob-ch04_s04_qs03_l07\" class=\"orderedlist\">\r\n \t<li>Mg or O<\/li>\r\n \t<li>S or F<\/li>\r\n \t<li>Al or Ga<\/li>\r\n \t<li>O or I<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa09\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p13\" class=\"para\">Will the electrons be shared equally or unequally across each covalent bond? If unequally, to which atom are the electrons more strongly drawn?<\/p>\r\n\r\n<ol id=\"gob-ch04_s04_qs03_l09\" class=\"orderedlist\">\r\n \t<li>a C\u2013O bond<\/li>\r\n \t<li>an F\u2013F bond<\/li>\r\n \t<li>an S\u2013N bond<\/li>\r\n \t<li>an I\u2013Cl bond<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch04_s04_qs03_qd01_qa10\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch04_s04_qs03_p14\" class=\"para\">Will the electrons be shared equally or unequally across each covalent bond? If unequally, to which atom are the electrons more strongly drawn?<\/p>\r\n\r\n<ol id=\"gob-ch04_s04_qs03_l11\" class=\"orderedlist\">\r\n \t<li>a C\u2013C bond<\/li>\r\n \t<li>a S\u2013Cl bond<\/li>\r\n \t<li>an O\u2013H bond<\/li>\r\n \t<li>an H\u2013H bond<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch04_s04_qs03_ans\" class=\"qandaset block\">\r\n<div class=\"answer\">\r\n<div class=\"textbox exercises\">\r\n<h3 class=\"title\">Answers<\/h3>\r\n[reveal-answer q=\"165622\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"165622\"]\r\n\r\n1. A C\u2013O bond is longer.\r\n\r\n3. a. 0.143 nm b. 0.120 nm c. 0.100 nm d. 0.116 nm\r\n\r\n5. Actual bond lengths are very small, so the nanometer unit makes the expression of length easier to understand.\r\n\r\n7. a. C b. O c. Na d. Cl\r\n\r\n9. a. unequally toward the O b. equally c. unequally toward the N d. unequally toward the Cl[\/hidden-answer]\r\n\r\n<\/div>\r\n<div class=\"textbox examples\">\r\n<h3>Further REading<\/h3>\r\n<ul>\r\n \t<li><a href=\"https:\/\/chem.libretexts.org\/LibreTexts\/University_of_Arkansas_Little_Rock\/2015_ChemInformatics%3A_Chem_4399%2F%2F5399\/Topics\/4A_Communicating_chemical_structure_with_formulas_and_names\">Communicating chemical structure with formulas and names<\/a><img class=\"size-thumbnail wp-image-4040 alignnone\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3369\/2018\/06\/26144658\/frame-2-150x150.png\" alt=\"\" width=\"150\" height=\"150\" \/><\/li>\r\n<\/ul>\r\n<\/div>\r\n&nbsp;\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>","rendered":"<div>\n<div class=\"section\" xml:lang=\"en\">\n<h2 id=\"gob-ch03_s01_p01\" class=\"para editable block\"><a id=\"1.3.1.\"><\/a>1.3.1. How and why atoms bond<\/h2>\n<div id=\"navbar-top\" class=\"navbar\">\n<div class=\"navbar-part left\">\n<div class=\"textbox learning-objectives\">\n<h3>Learning Objectives<\/h3>\n<div id=\"book-content\">\n<div id=\"gob-ch03_s01\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch03_s01_n01\" class=\"learning_objectives editable block\">\n<ol id=\"gob-ch03_s01_l01\" class=\"orderedlist\">\n<li>Define the octet rule.<\/li>\n<li>Describe how ionic bonds are formed.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p class=\"para editable block\">Atoms can join together by forming a <strong><span class=\"margin_term\"><span class=\"glossterm\">chemical bond<\/span><\/span>,<\/strong> which is a very strong attraction between two atoms. Chemical bonds are formed when electrons in different atoms interact with each other to make an arrangement that is more stable than when the atoms are apart.<\/p>\n<p id=\"gob-ch03_s01_p02\" class=\"para editable block\">What causes atoms to make a chemical bond with other atoms, rather than remaining as individual atoms? A clue comes by considering the noble gas elements, the rightmost column of the periodic table. These elements\u2014helium, neon, argon, krypton, xenon, and radon\u2014do not form compounds very easily, which suggests that they are especially stable as lone atoms. What else do the noble gas elements have in common? Except for helium, they all have eight valence electrons. Chemists have concluded that atoms are especially stable if they have eight electrons in their outermost shell. This useful rule of thumb is called the <strong><span class=\"margin_term\"><span class=\"glossterm\">octet rule<\/span><\/span><\/strong>, and it is a key to understanding why compounds form.<\/p>\n<p id=\"gob-ch03_s01_p04\" class=\"para editable block\">There are two ways for an atom that does not have an octet of valence electrons to obtain an octet in its outer shell. One way is the transfer of electrons between two atoms until all atoms have octets. Because some atoms will lose electrons and some atoms will gain electrons, there is no overall change in the number of electrons, but individual atoms acquire a nonzero electric charge. Those that lose electrons become positively charged, and those that gain electrons become negatively charged. Charged atoms are called <strong><span class=\"margin_term\"><span class=\"glossterm\">ions<\/span><\/span><\/strong>. Because opposite charges attract (while like charges repel), these oppositely charged ions attract each other, forming <strong><span class=\"margin_term\"><span class=\"glossterm\">ionic bonds<\/span><\/span>.<\/strong> The resulting compounds are called<strong> <span class=\"margin_term\"><span class=\"glossterm\">ionic compounds<\/span><\/span><\/strong>\u00a0and are the primary subject of this chapter.<\/p>\n<p id=\"gob-ch03_s01_p05\" class=\"para editable block\">The second way for an atom to obtain an octet of electrons is by sharing electrons with another atom. These shared electrons simultaneously occupy the outermost shell of more than one atom. The bond made by electron sharing is called a <strong class=\"emphasis bold\">covalent bond<\/strong>. Covalent bonding and covalent compounds will be discussed in detail below.<\/p>\n<div id=\"gob-ch03_s01_n03\" class=\"callout editable block\">\n<div class=\"textbox\">\n<p id=\"gob-ch03_s01_p06\" class=\"para\">NOTE: Despite our focus on the octet rule, we must remember that for small atoms, such as hydrogen, helium, and lithium, the first shell is, or becomes, the outermost shell and hold only two electrons. Therefore, these atoms satisfy a \u201cduet rule\u201d rather than the octet rule.<\/p>\n<\/div>\n<\/div>\n<div id=\"gob-ch03_s01_qs03\" class=\"qandaset block\">\n<div class=\"navbar\">\n<h2 class=\"navbar-part left\">1.3.2. Characteristics of covalent bonds<\/h2>\n<\/div>\n<div>\n<div id=\"gob-ch04_s04\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch04_s04_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<h3 class=\"title\">Learning Objective<\/h3>\n<ol id=\"gob-ch04_s04_l01\" class=\"orderedlist\">\n<li>Compare covalent bonds in terms of bond length and bond polarity.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<p id=\"gob-ch04_s04_p01\" class=\"para editable block\">Covalent bonds have certain characteristics that depend on the identities of the atoms participating in the bond. Two characteristics are bond length and bond polarity.<\/p>\n<div id=\"gob-ch04_s04_s01\" class=\"section\">\n<h3 class=\"title editable block\">Bond length<\/h3>\n<p id=\"gob-ch04_s04_s01_p01\" class=\"para editable block\">The covalent bond in the hydrogen molecule (H<sub class=\"subscript\">2<\/sub>) has a certain length (about 7.4 \u00d7 10<sup class=\"superscript\">\u221211<\/sup> m). Other covalent bonds also have known bond lengths, which are dependent on both the identities of the atoms in the bond and whether the bonds are single, double, or triple bonds. <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1.<\/a> lists the approximate bond lengths for some single covalent bonds. The exact bond length may vary depending on the identity of the molecule but will be close to the value given in the table.<\/p>\n<div id=\"gob-ch04_s04_s01_t01\" class=\"table block\">\n<h4 class=\"title\"><strong><span class=\"title-prefix\">Table 1.1.<\/span> Approximate bond lengths of some single bonds<\/strong><\/h4>\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\n<thead>\n<tr>\n<th>Bond<\/th>\n<th align=\"right\">Length (\u00d7 10<sup class=\"superscript\">\u221212<\/sup> m)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>H\u2013H<\/td>\n<td align=\"right\">74<\/td>\n<\/tr>\n<tr>\n<td>H\u2013C<\/td>\n<td align=\"right\">110<\/td>\n<\/tr>\n<tr>\n<td>H\u2013N<\/td>\n<td align=\"right\">100<\/td>\n<\/tr>\n<tr>\n<td>H\u2013O<\/td>\n<td align=\"right\">97<\/td>\n<\/tr>\n<tr>\n<td>H\u2013I<\/td>\n<td align=\"right\">161<\/td>\n<\/tr>\n<tr>\n<td>C\u2013C<\/td>\n<td align=\"right\">154<\/td>\n<\/tr>\n<tr>\n<td>C\u2013N<\/td>\n<td align=\"right\">147<\/td>\n<\/tr>\n<tr>\n<td>C\u2013O<\/td>\n<td align=\"right\">143<\/td>\n<\/tr>\n<tr>\n<td>N\u2013N<\/td>\n<td align=\"right\">145<\/td>\n<\/tr>\n<tr>\n<td>O\u2013O<\/td>\n<td align=\"right\">145<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<p id=\"gob-ch04_s04_s01_p02\" class=\"para editable block\"><a class=\"xref\" href=\"#gob-ch04_s04_s01_t02\">Table 1.2.<\/a> compares the lengths of single covalent bonds with those of double and triple bonds between the same atoms. Without exception, as the number of covalent bonds between two atoms increases, the bond length decreases. With more electrons between the two nuclei, the nuclei can get closer together before the internuclear repulsion is strong enough to balance the attraction.<\/p>\n<div id=\"gob-ch04_s04_s01_t02\" class=\"table block\">\n<h4 class=\"title\"><strong><span class=\"title-prefix\">Table 1.2.<\/span> Comparison of bond lengths for single and multiple bonds<\/strong><\/h4>\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\n<thead>\n<tr>\n<th>Bond<\/th>\n<th align=\"right\">Length (\u00d7 10<sup class=\"superscript\">\u221212<\/sup> m)<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>C\u2013C<\/td>\n<td align=\"right\">154<\/td>\n<\/tr>\n<tr>\n<td>C=C<\/td>\n<td align=\"right\">134<\/td>\n<\/tr>\n<tr>\n<td>C\u2261C<\/td>\n<td align=\"right\">120<\/td>\n<\/tr>\n<tr>\n<td>C\u2013N<\/td>\n<td align=\"right\">147<\/td>\n<\/tr>\n<tr>\n<td>C=N<\/td>\n<td align=\"right\">128<\/td>\n<\/tr>\n<tr>\n<td>C\u2261N<\/td>\n<td align=\"right\">116<\/td>\n<\/tr>\n<tr>\n<td>C\u2013O<\/td>\n<td align=\"right\">143<\/td>\n<\/tr>\n<tr>\n<td>C=O<\/td>\n<td align=\"right\">120<\/td>\n<\/tr>\n<tr>\n<td>C\u2261O<\/td>\n<td align=\"right\">113<\/td>\n<\/tr>\n<tr>\n<td>N\u2013N<\/td>\n<td align=\"right\">145<\/td>\n<\/tr>\n<tr>\n<td>N=N<\/td>\n<td align=\"right\">123<\/td>\n<\/tr>\n<tr>\n<td>N\u2261N<\/td>\n<td align=\"right\">110<\/td>\n<\/tr>\n<tr>\n<td>O\u2013O<\/td>\n<td align=\"right\">145<\/td>\n<\/tr>\n<tr>\n<td>O=O<\/td>\n<td align=\"right\">121<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<\/div>\n<div id=\"gob-ch04_s04_s02\" class=\"section\">\n<h3 class=\"title editable block\">Electronegativity and bond polarity<\/h3>\n<div style=\"width: 283px\" class=\"wp-caption alignright\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3369\/2018\/06\/22140559\/a63736e6eabf6300d625e2438ddfeaa7.jpg\" alt=\"image\" width=\"273\" height=\"468\" \/><\/p>\n<p class=\"wp-caption-text\"><em>Figure 1.6. Polar versus nonpolar covalent bonds. <\/em>(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.<\/p>\n<\/div>\n<p id=\"gob-ch04_s04_s02_p01\" class=\"para editable block\">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 <a class=\"xref\" href=\"#gob-ch04_s04_s02_f01\">Figure 1.6. &#8220;Polar versus Nonpolar Covalent Bonds&#8221;<\/a>. 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 <a class=\"xref\" href=\"#gob-ch04_s04_s02_f01\">Figure 1.6.<\/a>, is called a <span class=\"margin_term\"><span class=\"glossterm\"><strong>polar covalent bond<\/strong>. <\/span><\/span>A covalent bond that has an equal sharing of electrons (part (a) is called a <span class=\"margin_term\"><span class=\"glossterm\"><strong>nonpolar covalent bond<\/strong>.<\/span><\/span><\/p>\n<p id=\"gob-ch04_s04_s02_p02\" class=\"para editable block\">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 rather than shared. To judge the relative polarity of a covalent bond, chemists use <strong><span class=\"margin_term\"><span class=\"glossterm\">electronegativity<\/span><\/span>,<\/strong> which is a relative measure of how strongly an atom attracts electrons when it forms a covalent bond. There are various numerical scales for rating electronegativity. <a class=\"xref\" href=\"#gob-ch04_s04_s02_f02\">Figure 1.7. &#8220;Electronegativities of Various Elements&#8221;<\/a> shows one of the most popular\u2014the Pauling scale. The polarity of a covalent bond can be judged by determining the difference in the electronegativities of the two atoms making the bond. The greater the difference in electronegativities, the greater the imbalance of electron sharing in the bond. Although there are no hard and fast rules, the general rule is if the difference in electronegativities is less than about 0.4, the bond is considered nonpolar; if the difference is greater than 0.4, the bond is considered polar. If 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.<\/p>\n<p>When a molecule\u2019s bonds are polar, the substance is usually found to be 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.)\u00a0 This aspect will be discussed in more detail in <a href=\"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/chapter\/1-8-intermolecular-forces\/\">section 1.8. on intermolecular forces<\/a>.<\/p>\n<div id=\"gob-ch04_s04_s02_f02\" class=\"figure large editable block\">\n<div style=\"width: 1548px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3369\/2018\/06\/22140603\/0b3884eacaf2db8be97ff0dc7ccaaae1.jpg\" alt=\"image\" width=\"1538\" height=\"996\" \/><\/p>\n<p class=\"wp-caption-text\"><em>Figure 1.7. Electronegativities of Various Elements.\u00a0<\/em>A popular scale for electronegativities has the value for fluorine atoms set at 4.0, the highest value.<\/p>\n<\/div>\n<p class=\"para\">\n<\/div>\n<div id=\"gob-ch04_s04_s02_n01\" class=\"callout block\">\n<div class=\"textbox shaded\">\n<h3 class=\"title\">Looking Closer: Linus Pauling<\/h3>\n<p id=\"gob-ch04_s04_s02_p03\" class=\"para\">Arguably the most influential chemist of the 20th century, Linus Pauling (1901\u201394) is the only person to have won two individual (that is, unshared) Nobel Prizes. In the 1930s, Pauling used new mathematical theories to enunciate some fundamental principles of the chemical bond. His 1939 book <em class=\"emphasis\">The Nature of the Chemical Bond<\/em> is one of the most significant books ever published in chemistry.<\/p>\n<p id=\"gob-ch04_s04_s02_p04\" class=\"para\">By 1935, Pauling\u2019s interest turned to biological molecules, and he was awarded the 1954 Nobel Prize in Chemistry for his work on protein structure. (He was very close to discovering the double helix structure of DNA when James Watson and James Crick announced their own discovery of its structure in 1953.) He was later awarded the 1962 Nobel Peace Prize for his efforts to ban the testing of nuclear weapons.<\/p>\n<p id=\"gob-ch04_s04_s02_p05\" class=\"para\">In his later years, Pauling became convinced that large doses of vitamin C would prevent disease, including the common cold. Most clinical research failed to show a connection, but Pauling continued to take large doses daily. He died in 1994, having spent a lifetime establishing a scientific legacy that few will ever equal.<\/p>\n<div class=\"informalfigure medium\">\n<div style=\"width: 197px\" class=\"wp-caption alignright\"><img loading=\"lazy\" decoding=\"async\" class=\"\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3369\/2018\/06\/22140606\/df9a49acad271a13b8e3a5fd85e30b33.jpg\" alt=\"image\" width=\"187\" height=\"288\" \/><\/p>\n<p class=\"wp-caption-text\"><em>Linus Pauling was one of the most influential chemists of the 20th century.<\/em><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch04_s04_s02_n02\" class=\"exercises editable block\">\n<h3 class=\"title\">Example 2<\/h3>\n<p id=\"gob-ch04_s04_s02_p06\" class=\"para\">Describe the electronegativity difference between each pair of atoms and the resulting polarity (or bond type).<\/p>\n<ol id=\"gob-ch04_s04_s02_l01\" class=\"orderedlist\">\n<li>C and H<\/li>\n<li>H and H<\/li>\n<li>Na and Cl<\/li>\n<li>O and H<\/li>\n<\/ol>\n<p class=\"simpara\">Solution<\/p>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q979132\">Show Answer<\/span><\/p>\n<div id=\"q979132\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li>Carbon has an electronegativity of 2.5, while the value for hydrogen is 2.1. The difference is 0.3, which is rather small. The C\u2013H bond is therefore considered nonpolar.<\/li>\n<li>Both hydrogen atoms have the same electronegativity value\u20142.1. The difference is zero, so the bond is nonpolar.<\/li>\n<li>Sodium\u2019s electronegativity is 0.9, while chlorine\u2019s is 3.0. The difference is 2.1, which is rather high, and so sodium and chlorine form an ionic compound.<\/li>\n<li>With 2.1 for hydrogen and 3.5 for oxygen, the electronegativity difference is 1.4. We would expect a very polar bond, but not so polar that the O\u2013H bond is considered ionic.<\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch04_s04_qs01\" class=\"qandaset block\">\n<div class=\"textbox shaded\">\n<h3 class=\"title\">Skill-Building Exercise<\/h3>\n<ol id=\"gob-ch04_s04_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch04_s04_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs01_p02\" class=\"para\">C and O<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs01_p04\" class=\"para\">K and Br<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs01_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs01_p06\" class=\"para\">N and N<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs01_qd01_qa04\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs01_p08\" class=\"para\">Cs and F<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<div id=\"gob-ch04_s04_qs02\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<ol id=\"gob-ch04_s04_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch04_s04_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs02_p01\" class=\"para\">What is the name for the distance between two atoms in a covalent bond?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs02_p03\" class=\"para\">What does the electronegativity of an atom indicate?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs02_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs02_p05\" class=\"para\">What type of bond is formed between two atoms if the difference in electronegativities is small? Medium? Large?<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<div class=\"textbox exercises\">\n<div class=\"qandaset block\">\n<h3 class=\"title\">Answers<\/h3>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q557987\">Show Answer<\/span><\/p>\n<div id=\"q557987\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li>bond length<\/li>\n<li>Electronegativity is a qualitative measure of how much an atom attracts electrons in a covalent bond.<\/li>\n<li>nonpolar; polar; ionic<\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch04_s04_s02_n05\" class=\"key_takeaways editable block\">\n<div class=\"textbox key-takeaways\">\n<h3 class=\"title\">Key Takeaways<\/h3>\n<ul id=\"gob-ch04_s04_s02_l05\" class=\"itemizedlist\">\n<li>Covalent bonds between different atoms have different bond lengths.<\/li>\n<li>Covalent bonds can be polar or nonpolar, depending on the electronegativity difference between the atoms involved.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div id=\"gob-ch04_s04_qs03\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<h3>Exercises<\/h3>\n<ol id=\"gob-ch04_s04_qs03_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch04_s04_qs03_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p01\" class=\"para\">Which is longer\u2014a C\u2013H bond or a C\u2013O bond? (Refer to <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1. &#8220;Approximate Bond Lengths of Some Single Bonds&#8221;<\/a>.)<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p03\" class=\"para\">Which is shorter\u2014an N\u2013H bond or a C\u2013H bond? (Refer to <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1. &#8220;Approximate Bond Lengths of Some Single Bonds&#8221;<\/a>.)<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p05\" class=\"para\">A nanometer is 10<sup class=\"superscript\">\u22129<\/sup> m. Using the data in <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1. &#8220;Approximate Bond Lengths of Some Single Bonds&#8221;<\/a> and <a class=\"xref\" href=\"#gob-ch04_s04_s01_t02\">Table 1.2. &#8220;Comparison of Bond Lengths for Single and Multiple Bonds&#8221;<\/a>, determine the length of each bond in nanometers.<\/p>\n<ol id=\"gob-ch04_s04_qs03_l01\" class=\"orderedlist\">\n<li>a C\u2013O bond<\/li>\n<li>a C=O bond<\/li>\n<li>an H\u2013N bond<\/li>\n<li>a C\u2261N bond<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa04\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p06\" class=\"para\">An angstrom (\u00c5) is defined as 10<sup class=\"superscript\">\u221210<\/sup> m. Using <a class=\"xref\" href=\"#gob-ch04_s04_s01_t01\">Table 1.1. &#8220;Approximate Bond Lengths of Some Single Bonds&#8221;<\/a> and <a class=\"xref\" href=\"#gob-ch04_s04_s01_t02\">Table 1.2. &#8220;Comparison of Bond Lengths for Single and Multiple Bonds&#8221;<\/a>, determine the length of each bond in angstroms.<\/p>\n<ol id=\"gob-ch04_s04_qs03_l03\" class=\"orderedlist\">\n<li>a C\u2013C bond<\/li>\n<li>a C=C bond<\/li>\n<li>an N\u2261N bond<\/li>\n<li>an H\u2013O bond<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa05\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p07\" class=\"para\">Refer to Exercise 3. Why is the nanometer unit useful as a unit for expressing bond lengths?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa06\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p09\" class=\"para\">Refer to Exercise 4. Why is the angstrom unit useful as a unit for expressing bond lengths?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa07\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p11\" class=\"para\">Using <a class=\"xref\" href=\"#gob-ch04_s04_s02_f02\">Figure 1.7. &#8220;Electronegativities of Various Elements&#8221;<\/a>, determine which atom in each pair has the higher electronegativity.<\/p>\n<ol id=\"gob-ch04_s04_qs03_l05\" class=\"orderedlist\">\n<li>H or C<\/li>\n<li>O or Br<\/li>\n<li>Na or Rb<\/li>\n<li>I or Cl<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa08\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p12\" class=\"para\">Using <a class=\"xref\" href=\"#gob-ch04_s04_s02_f02\">Figure 1.7. &#8220;Electronegativities of Various Elements&#8221;<\/a>, determine which atom in each pair has the lower electronegativity.<\/p>\n<ol id=\"gob-ch04_s04_qs03_l07\" class=\"orderedlist\">\n<li>Mg or O<\/li>\n<li>S or F<\/li>\n<li>Al or Ga<\/li>\n<li>O or I<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa09\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p13\" class=\"para\">Will the electrons be shared equally or unequally across each covalent bond? If unequally, to which atom are the electrons more strongly drawn?<\/p>\n<ol id=\"gob-ch04_s04_qs03_l09\" class=\"orderedlist\">\n<li>a C\u2013O bond<\/li>\n<li>an F\u2013F bond<\/li>\n<li>an S\u2013N bond<\/li>\n<li>an I\u2013Cl bond<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch04_s04_qs03_qd01_qa10\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch04_s04_qs03_p14\" class=\"para\">Will the electrons be shared equally or unequally across each covalent bond? If unequally, to which atom are the electrons more strongly drawn?<\/p>\n<ol id=\"gob-ch04_s04_qs03_l11\" class=\"orderedlist\">\n<li>a C\u2013C bond<\/li>\n<li>a S\u2013Cl bond<\/li>\n<li>an O\u2013H bond<\/li>\n<li>an H\u2013H bond<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<div id=\"gob-ch04_s04_qs03_ans\" class=\"qandaset block\">\n<div class=\"answer\">\n<div class=\"textbox exercises\">\n<h3 class=\"title\">Answers<\/h3>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q165622\">Show Answer<\/span><\/p>\n<div id=\"q165622\" class=\"hidden-answer\" style=\"display: none\">\n<p>1. A C\u2013O bond is longer.<\/p>\n<p>3. a. 0.143 nm b. 0.120 nm c. 0.100 nm d. 0.116 nm<\/p>\n<p>5. Actual bond lengths are very small, so the nanometer unit makes the expression of length easier to understand.<\/p>\n<p>7. a. C b. O c. Na d. Cl<\/p>\n<p>9. a. unequally toward the O b. equally c. unequally toward the N d. unequally toward the Cl<\/p><\/div>\n<\/div>\n<\/div>\n<div class=\"textbox examples\">\n<h3>Further REading<\/h3>\n<ul>\n<li><a href=\"https:\/\/chem.libretexts.org\/LibreTexts\/University_of_Arkansas_Little_Rock\/2015_ChemInformatics%3A_Chem_4399%2F%2F5399\/Topics\/4A_Communicating_chemical_structure_with_formulas_and_names\">Communicating chemical structure with formulas and names<\/a><img loading=\"lazy\" decoding=\"async\" class=\"size-thumbnail wp-image-4040 alignnone\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3369\/2018\/06\/26144658\/frame-2-150x150.png\" alt=\"\" width=\"150\" height=\"150\" \/><\/li>\n<\/ul>\n<\/div>\n<p>&nbsp;<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\t\t\t <section class=\"citations-section\" role=\"contentinfo\">\n\t\t\t <h3>Candela Citations<\/h3>\n\t\t\t\t\t <div>\n\t\t\t\t\t\t <div id=\"citation-list-3098\">\n\t\t\t\t\t\t\t <div class=\"licensing\"><div class=\"license-attribution-dropdown-subheading\">CC licensed content, Shared previously<\/div><ul class=\"citation-list\"><li>The Basics of General, Organic, and Biological Chemistry v. 1.0. <strong>Provided by<\/strong>: Saylor Academy. <strong>Located at<\/strong>: <a target=\"_blank\" href=\"https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/\">https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/<\/a>. <strong>License<\/strong>: <em><a target=\"_blank\" rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/\">CC BY-NC: Attribution-NonCommercial<\/a><\/em>. <strong>License Terms<\/strong>: This text was adapted by Saylor Academy under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License without attribution as requested by the work&#039;s original creator or licensor.<\/li><\/ul><\/div>\n\t\t\t\t\t\t <\/div>\n\t\t\t\t\t <\/div>\n\t\t\t <\/section>","protected":false},"author":311,"menu_order":3,"template":"","meta":{"_candela_citation":"[{\"type\":\"cc\",\"description\":\"The Basics of General, Organic, and Biological Chemistry v. 1.0\",\"author\":\"\",\"organization\":\"Saylor Academy\",\"url\":\"https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/\",\"project\":\"\",\"license\":\"cc-by-nc\",\"license_terms\":\"This text was adapted by Saylor Academy under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License without attribution as requested by the work\\'s original creator or licensor.\"}]","CANDELA_OUTCOMES_GUID":"","pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":[],"pb_section_license":""},"chapter-type":[],"contributor":[],"license":[],"class_list":["post-3098","chapter","type-chapter","status-publish","hentry"],"part":2222,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/pressbooks\/v2\/chapters\/3098","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/wp\/v2\/users\/311"}],"version-history":[{"count":22,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/pressbooks\/v2\/chapters\/3098\/revisions"}],"predecessor-version":[{"id":4730,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/pressbooks\/v2\/chapters\/3098\/revisions\/4730"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/pressbooks\/v2\/parts\/2222"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/pressbooks\/v2\/chapters\/3098\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/wp\/v2\/media?parent=3098"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=3098"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/wp\/v2\/contributor?post=3098"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry\/wp-json\/wp\/v2\/license?post=3098"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}