{"id":957,"date":"2018-03-20T16:48:30","date_gmt":"2018-03-20T16:48:30","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/?post_type=chapter&#038;p=957"},"modified":"2018-10-22T20:37:19","modified_gmt":"2018-10-22T20:37:19","slug":"12-2-structures-and-names-of-alkanes","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/12-2-structures-and-names-of-alkanes\/","title":{"raw":"12.2 Structures and Names of Alkanes","rendered":"12.2 Structures and Names of Alkanes"},"content":{"raw":"<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-ch12_s02\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch12_s02_n01\" class=\"learning_objectives editable block\">\r\n<ol id=\"gob-ch12_s02_l01\" class=\"orderedlist\">\r\n \t<li>Identify and name simple (straight-chain) alkanes given formulas and write formulas for straight-chain alkanes given their names.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n&nbsp;\r\n\r\n<\/div>\r\n<\/div>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch12_s02\" class=\"section\" xml:lang=\"en\">\r\n<p id=\"gob-ch12_s02_p01\" class=\"para editable block\">We began our study of organic chemistry in <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-4\">Chapter 4 \"Covalent Bonding and Simple Molecular Compounds\"<\/a> with the <span class=\"margin_term\"><strong><span class=\"glossterm\">hydrocarbons<\/span><\/strong><\/span>, the simplest organic compounds, which are composed of carbon and hydrogen atoms only. As we noted, there are several different kinds of hydrocarbons. They are distinguished by the types of bonding between carbon atoms and the properties that result from that bonding. Hydrocarbons with only carbon-to-carbon single bonds (C\u2013C) and existing as a continuous chain of carbon atoms also bonded to hydrogen atoms are called <span class=\"margin_term\"><strong><span class=\"glossterm\">alkanes (or saturated hydrocarbons)<\/span><\/strong><\/span>. <em class=\"emphasis\">Saturated<\/em>, in this case, means that each carbon atom is bonded to four other atoms (hydrogen or carbon)\u2014the most possible; there are no double or triple bonds in the molecules.<\/p>\r\n\r\n<div id=\"gob-ch12_s02_n02\" class=\"callout editable block\">\r\n<div class=\"textbox\">\r\n<h3 class=\"title\">Note<\/h3>\r\n<p id=\"gob-ch12_s02_p02\" class=\"para\">The word <em class=\"emphasis\">saturated<\/em> has the same meaning for hydrocarbons as it does for the dietary fats and oils: the molecule has no carbon-to-carbon double bonds (C=C). (For more information about fats and oils, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-17\">Chapter 17 \"Lipids\"<\/a>, <a class=\"xref\" href=\"gob-ch17_s01#gob-ch17_s01\">Section 17.1 \"Fatty Acids\"<\/a> and <a class=\"xref\" href=\"gob-ch17_s02#gob-ch17_s02\">Section 17.2 \"Fats and Oils\"<\/a>.)<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<p id=\"gob-ch12_s02_p03\" class=\"para editable block\">We introduced the three simplest alkanes\u2014methane (CH<sub class=\"subscript\">4<\/sub>), ethane (C<sub class=\"subscript\">2<\/sub>H<sub class=\"subscript\">6<\/sub>), and propane (C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub>)\u2014in <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-4\">Chapter 4 \"Covalent Bonding and Simple Molecular Compounds\"<\/a>, <a class=\"xref\" href=\"gob-ch04_s06#gob-ch04_s06\">Section 4.6 \"Introduction to Organic Chemistry\"<\/a>. They are shown again in <a class=\"xref\" href=\"#gob-ch12_s02_f01\">Figure 12.1 \"The Three Simplest Alkanes\"<\/a>. The flat representations shown do not accurately portray bond angles or molecular geometry. Methane has a tetrahedral shape that chemists often portray with wedges indicating bonds coming out toward you and dashed lines indicating bonds that go back away from you. (For more information about the shape of molecules, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-4\">Chapter 4 \"Covalent Bonding and Simple Molecular Compounds\"<\/a>, <a class=\"xref\" href=\"gob-ch04_s05#gob-ch04_s05\">Section 4.5 \"Characteristics of Molecules\"<\/a>.) An ordinary solid line indicates a bond in the plane of the page.<\/p>\r\n\r\n<div id=\"gob-ch12_s02_f01\" class=\"figure large editable block\">\r\n\r\n[caption id=\"\" align=\"aligncenter\" width=\"1504\"]<img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/20164757\/ceb9608ec0b972189e25b54fb971bb57.jpg\" alt=\"image\" width=\"1504\" height=\"420\" \/> <em>Figure 12.1 The Three Simplest Alkanes<\/em>[\/caption]\r\n\r\n<\/div>\r\n<p id=\"gob-ch12_s02_p04\" class=\"para editable block\">Recall from <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-4\">Chapter 4 \"Covalent Bonding and Simple Molecular Compounds\"<\/a>, <a class=\"xref\" href=\"gob-ch04_s05#gob-ch04_s05\">Section 4.5 \"Characteristics of Molecules\"<\/a> that the VSEPR theory correctly predicts a tetrahedral shape for the methane molecule (<a class=\"xref\" href=\"#gob-ch12_s02_f02\">Figure 12.2 \"The Tetrahedral Methane Molecule\"<\/a>).<\/p>\r\n\r\n<div id=\"gob-ch12_s02_f02\" class=\"figure large editable block\">\r\n\r\n[caption id=\"\" align=\"aligncenter\" width=\"1504\"]<img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/20164800\/74e55c16576f4ef795c2e985c1ca20d1.jpg\" alt=\"image\" width=\"1504\" height=\"519\" \/> <em>Figure 12.2 The Tetrahedral Methane Molecule<\/em>[\/caption]\r\n\r\n<\/div>\r\n<p id=\"gob-ch12_s02_p05\" class=\"para editable block\">Methane (CH<sub class=\"subscript\">4<\/sub>), ethane (C<sub class=\"subscript\">2<\/sub>H<sub class=\"subscript\">6<\/sub>), and propane (C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub>) are the beginning of a series of compounds in which any two members in a sequence differ by one carbon atom and two hydrogen atoms\u2014namely, a CH<sub class=\"subscript\">2<\/sub> unit. The first 10 members of this series are given in <a class=\"xref\" href=\"#gob-ch12_s02_t01\">Table 12.2 \"The First 10 Straight-Chain Alkanes\"<\/a>.<\/p>\r\n\r\n<div id=\"gob-ch12_s02_t01\" class=\"table block\">\r\n<h5 class=\"title\"><strong><span class=\"title-prefix\">Table 12.2<\/span> The First 10 Straight-Chain Alkanes<\/strong><\/h5>\r\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\r\n<thead>\r\n<tr>\r\n<th style=\"width: 62px\">Name<\/th>\r\n<th style=\"width: 195px\">Molecular Formula (C<sub class=\"subscript\"><em class=\"emphasis\">n<\/em><\/sub>H<sub class=\"subscript\">2<\/sub><sub class=\"subscript\"><em class=\"emphasis\">n<\/em><\/sub> <sub class=\"subscript\">+ 2<\/sub>)<\/th>\r\n<th style=\"width: 256px\">Condensed Structural Formula for Continuous Chain<\/th>\r\n<th style=\"width: 185px\" align=\"right\">Number of Possible Isomers<\/th>\r\n<\/tr>\r\n<\/thead>\r\n<tbody>\r\n<tr>\r\n<td style=\"width: 62px\">methane<\/td>\r\n<td style=\"width: 195px\">CH<sub class=\"subscript\">4<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">4<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">\u2014<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">ethane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">2<\/sub>H<sub class=\"subscript\">6<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">\u2014<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">propane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">\u2014<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">butane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">4<\/sub>H<sub class=\"subscript\">10<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">2<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">pentane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">5<\/sub>H<sub class=\"subscript\">12<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">3<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">hexane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">6<\/sub>H<sub class=\"subscript\">14<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">5<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">heptane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">7<\/sub>H<sub class=\"subscript\">16<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">9<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">octane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">8<\/sub>H<sub class=\"subscript\">18<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">18<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">nonane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">9<\/sub>H<sub class=\"subscript\">20<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">35<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 62px\">decane<\/td>\r\n<td style=\"width: 195px\">C<sub class=\"subscript\">10<\/sub>H<sub class=\"subscript\">22<\/sub><\/td>\r\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\r\n<td style=\"width: 185px\" align=\"right\">75<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<\/div>\r\n<p id=\"gob-ch12_s02_p06\" class=\"para editable block\">Consider the series in <a class=\"xref\" href=\"#gob-ch12_s02_f03\">Figure 12.3 \"Members of a Homologous Series\"<\/a>. The sequence starts with C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub>, and a CH<sub class=\"subscript\">2<\/sub> unit is added in each step moving up the series. Any family of compounds in which adjacent members differ from each other by a definite factor (here a CH<sub class=\"subscript\">2<\/sub> group) is called a <span class=\"margin_term\"><strong><span class=\"glossterm\">homologous series<\/span><\/strong><\/span>. The members of such a series, called <em class=\"emphasis\">homologs<\/em>, have properties that vary in a regular and predictable manner. The principle of <em class=\"emphasis\">homology<\/em> gives organization to organic chemistry in much the same way that the periodic table gives organization to inorganic chemistry. Instead of a bewildering array of individual carbon compounds, we can study a few members of a homologous series and from them deduce some of the properties of other compounds in the series.<\/p>\r\n\r\n<div id=\"gob-ch12_s02_f03\" class=\"figure large editable block\">\r\n\r\n[caption id=\"\" align=\"aligncenter\" width=\"1759\"]<img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/20164802\/1e8b019bfe6949342d49dc98e9c1335f.jpg\" alt=\"image\" width=\"1759\" height=\"807\" \/> <em>Figure 12.3 Members of a Homologous Series.\u00a0<\/em>Each succeeding formula incorporates one carbon atom and two hydrogen atoms more than the previous formula.[\/caption]\r\n\r\n<\/div>\r\n<p id=\"gob-ch12_s02_p07\" class=\"para editable block\">The principle of homology allows us to write a general formula for alkanes: C<sub class=\"subscript\"><em class=\"emphasis\">n<\/em><\/sub>H<sub class=\"subscript\">2<\/sub><sub class=\"subscript\"><em class=\"emphasis\">n<\/em><\/sub> <sub class=\"subscript\">+ 2<\/sub>. Using this formula, we can write a molecular formula for any alkane with a given number of carbon atoms. For example, an alkane with eight carbon atoms has the molecular formula C<sub class=\"subscript\">8<\/sub>H<sub class=\"subscript\">(2 \u00d7 8) + 2<\/sub> = C<sub class=\"subscript\">8<\/sub>H<sub class=\"subscript\">18<\/sub>.<\/p>\r\n\r\n<div id=\"gob-ch12_s02_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch12_s02_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<ol id=\"gob-ch12_s02_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch12_s02_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s02_qs01_p01\" class=\"para\">In the homologous series of alkanes, what is the molecular formula for the member just above C<sub class=\"subscript\">8<\/sub>H<sub class=\"subscript\">18<\/sub>?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch12_s02_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s02_qs01_p03\" class=\"para\">Use the general formula for alkanes to write the molecular formula of the alkane with 12 carbon atoms.<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch12_s02_qs01_ans\" class=\"qandaset block\">\r\n<h3 class=\"title\">Answers<\/h3>\r\n[reveal-answer q=\"872574\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"872574\"]\r\n<ol>\r\n \t<li>C<sub>9<\/sub>H<sub>20<\/sub><\/li>\r\n \t<li>C<sub>12<\/sub>H<sub>26<\/sub>\u00a0[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox key-takeaways\">\r\n<div id=\"gob-ch12_s02_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Key Takeaway<\/h3>\r\n<\/div>\r\n<div id=\"gob-ch12_s02_n04\" class=\"key_takeaways editable block\">\r\n<ul id=\"gob-ch12_s02_l03\" class=\"itemizedlist\">\r\n \t<li>Simple alkanes exist as a homologous series, in which adjacent members differ by a CH<sub class=\"subscript\">2<\/sub> unit.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch12_s02_qs02\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<h3>Exercises<\/h3>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch12_s02\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch12_s02_qs02\" class=\"qandaset block\">\r\n<h3 class=\"title\">Exercises<\/h3>\r\n<ol id=\"gob-ch12_s02_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch12_s02_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s02_qs02_p01\" class=\"para\">What compounds contain fewer carbon atoms than C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub> and are its homologs?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch12_s02_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s02_qs02_p03\" class=\"para\">What compounds contain five to eight carbon atoms and are homologs of C<sub class=\"subscript\">4<\/sub>H<sub class=\"subscript\">10<\/sub>?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch12_s02_qs02_ans\" class=\"qandaset block\">\r\n<h3 class=\"title\">Answer<\/h3>\r\n[reveal-answer q=\"679453\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"679453\"]1. CH<sub>4<\/sub> and C<sub>2<\/sub>H<sub>6<\/sub> \u00a0[\/hidden-answer]\r\n<div class=\"answer\"><\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n&nbsp;\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>","rendered":"<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-ch12_s02\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch12_s02_n01\" class=\"learning_objectives editable block\">\n<ol id=\"gob-ch12_s02_l01\" class=\"orderedlist\">\n<li>Identify and name simple (straight-chain) alkanes given formulas and write formulas for straight-chain alkanes given their names.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p>&nbsp;<\/p>\n<\/div>\n<\/div>\n<div id=\"book-content\">\n<div id=\"gob-ch12_s02\" class=\"section\" xml:lang=\"en\">\n<p id=\"gob-ch12_s02_p01\" class=\"para editable block\">We began our study of organic chemistry in <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-4\">Chapter 4 &#8220;Covalent Bonding and Simple Molecular Compounds&#8221;<\/a> with the <span class=\"margin_term\"><strong><span class=\"glossterm\">hydrocarbons<\/span><\/strong><\/span>, the simplest organic compounds, which are composed of carbon and hydrogen atoms only. As we noted, there are several different kinds of hydrocarbons. They are distinguished by the types of bonding between carbon atoms and the properties that result from that bonding. Hydrocarbons with only carbon-to-carbon single bonds (C\u2013C) and existing as a continuous chain of carbon atoms also bonded to hydrogen atoms are called <span class=\"margin_term\"><strong><span class=\"glossterm\">alkanes (or saturated hydrocarbons)<\/span><\/strong><\/span>. <em class=\"emphasis\">Saturated<\/em>, in this case, means that each carbon atom is bonded to four other atoms (hydrogen or carbon)\u2014the most possible; there are no double or triple bonds in the molecules.<\/p>\n<div id=\"gob-ch12_s02_n02\" class=\"callout editable block\">\n<div class=\"textbox\">\n<h3 class=\"title\">Note<\/h3>\n<p id=\"gob-ch12_s02_p02\" class=\"para\">The word <em class=\"emphasis\">saturated<\/em> has the same meaning for hydrocarbons as it does for the dietary fats and oils: the molecule has no carbon-to-carbon double bonds (C=C). (For more information about fats and oils, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-17\">Chapter 17 &#8220;Lipids&#8221;<\/a>, <a class=\"xref\" href=\"gob-ch17_s01#gob-ch17_s01\">Section 17.1 &#8220;Fatty Acids&#8221;<\/a> and <a class=\"xref\" href=\"gob-ch17_s02#gob-ch17_s02\">Section 17.2 &#8220;Fats and Oils&#8221;<\/a>.)<\/p>\n<\/div>\n<\/div>\n<p id=\"gob-ch12_s02_p03\" class=\"para editable block\">We introduced the three simplest alkanes\u2014methane (CH<sub class=\"subscript\">4<\/sub>), ethane (C<sub class=\"subscript\">2<\/sub>H<sub class=\"subscript\">6<\/sub>), and propane (C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub>)\u2014in <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-4\">Chapter 4 &#8220;Covalent Bonding and Simple Molecular Compounds&#8221;<\/a>, <a class=\"xref\" href=\"gob-ch04_s06#gob-ch04_s06\">Section 4.6 &#8220;Introduction to Organic Chemistry&#8221;<\/a>. They are shown again in <a class=\"xref\" href=\"#gob-ch12_s02_f01\">Figure 12.1 &#8220;The Three Simplest Alkanes&#8221;<\/a>. The flat representations shown do not accurately portray bond angles or molecular geometry. Methane has a tetrahedral shape that chemists often portray with wedges indicating bonds coming out toward you and dashed lines indicating bonds that go back away from you. (For more information about the shape of molecules, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-4\">Chapter 4 &#8220;Covalent Bonding and Simple Molecular Compounds&#8221;<\/a>, <a class=\"xref\" href=\"gob-ch04_s05#gob-ch04_s05\">Section 4.5 &#8220;Characteristics of Molecules&#8221;<\/a>.) An ordinary solid line indicates a bond in the plane of the page.<\/p>\n<div id=\"gob-ch12_s02_f01\" class=\"figure large editable block\">\n<div style=\"width: 1514px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/20164757\/ceb9608ec0b972189e25b54fb971bb57.jpg\" alt=\"image\" width=\"1504\" height=\"420\" \/><\/p>\n<p class=\"wp-caption-text\"><em>Figure 12.1 The Three Simplest Alkanes<\/em><\/p>\n<\/div>\n<\/div>\n<p id=\"gob-ch12_s02_p04\" class=\"para editable block\">Recall from <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-4\">Chapter 4 &#8220;Covalent Bonding and Simple Molecular Compounds&#8221;<\/a>, <a class=\"xref\" href=\"gob-ch04_s05#gob-ch04_s05\">Section 4.5 &#8220;Characteristics of Molecules&#8221;<\/a> that the VSEPR theory correctly predicts a tetrahedral shape for the methane molecule (<a class=\"xref\" href=\"#gob-ch12_s02_f02\">Figure 12.2 &#8220;The Tetrahedral Methane Molecule&#8221;<\/a>).<\/p>\n<div id=\"gob-ch12_s02_f02\" class=\"figure large editable block\">\n<div style=\"width: 1514px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/20164800\/74e55c16576f4ef795c2e985c1ca20d1.jpg\" alt=\"image\" width=\"1504\" height=\"519\" \/><\/p>\n<p class=\"wp-caption-text\"><em>Figure 12.2 The Tetrahedral Methane Molecule<\/em><\/p>\n<\/div>\n<\/div>\n<p id=\"gob-ch12_s02_p05\" class=\"para editable block\">Methane (CH<sub class=\"subscript\">4<\/sub>), ethane (C<sub class=\"subscript\">2<\/sub>H<sub class=\"subscript\">6<\/sub>), and propane (C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub>) are the beginning of a series of compounds in which any two members in a sequence differ by one carbon atom and two hydrogen atoms\u2014namely, a CH<sub class=\"subscript\">2<\/sub> unit. The first 10 members of this series are given in <a class=\"xref\" href=\"#gob-ch12_s02_t01\">Table 12.2 &#8220;The First 10 Straight-Chain Alkanes&#8221;<\/a>.<\/p>\n<div id=\"gob-ch12_s02_t01\" class=\"table block\">\n<h5 class=\"title\"><strong><span class=\"title-prefix\">Table 12.2<\/span> The First 10 Straight-Chain Alkanes<\/strong><\/h5>\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\n<thead>\n<tr>\n<th style=\"width: 62px\">Name<\/th>\n<th style=\"width: 195px\">Molecular Formula (C<sub class=\"subscript\"><em class=\"emphasis\">n<\/em><\/sub>H<sub class=\"subscript\">2<\/sub><sub class=\"subscript\"><em class=\"emphasis\">n<\/em><\/sub> <sub class=\"subscript\">+ 2<\/sub>)<\/th>\n<th style=\"width: 256px\">Condensed Structural Formula for Continuous Chain<\/th>\n<th style=\"width: 185px\" align=\"right\">Number of Possible Isomers<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td style=\"width: 62px\">methane<\/td>\n<td style=\"width: 195px\">CH<sub class=\"subscript\">4<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">4<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">\u2014<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">ethane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">2<\/sub>H<sub class=\"subscript\">6<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">\u2014<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">propane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">\u2014<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">butane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">4<\/sub>H<sub class=\"subscript\">10<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">2<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">pentane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">5<\/sub>H<sub class=\"subscript\">12<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">3<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">hexane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">6<\/sub>H<sub class=\"subscript\">14<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">5<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">heptane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">7<\/sub>H<sub class=\"subscript\">16<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">9<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">octane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">8<\/sub>H<sub class=\"subscript\">18<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">18<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">nonane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">9<\/sub>H<sub class=\"subscript\">20<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">35<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 62px\">decane<\/td>\n<td style=\"width: 195px\">C<sub class=\"subscript\">10<\/sub>H<sub class=\"subscript\">22<\/sub><\/td>\n<td style=\"width: 256px\">CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub><\/td>\n<td style=\"width: 185px\" align=\"right\">75<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<p id=\"gob-ch12_s02_p06\" class=\"para editable block\">Consider the series in <a class=\"xref\" href=\"#gob-ch12_s02_f03\">Figure 12.3 &#8220;Members of a Homologous Series&#8221;<\/a>. The sequence starts with C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub>, and a CH<sub class=\"subscript\">2<\/sub> unit is added in each step moving up the series. Any family of compounds in which adjacent members differ from each other by a definite factor (here a CH<sub class=\"subscript\">2<\/sub> group) is called a <span class=\"margin_term\"><strong><span class=\"glossterm\">homologous series<\/span><\/strong><\/span>. The members of such a series, called <em class=\"emphasis\">homologs<\/em>, have properties that vary in a regular and predictable manner. The principle of <em class=\"emphasis\">homology<\/em> gives organization to organic chemistry in much the same way that the periodic table gives organization to inorganic chemistry. Instead of a bewildering array of individual carbon compounds, we can study a few members of a homologous series and from them deduce some of the properties of other compounds in the series.<\/p>\n<div id=\"gob-ch12_s02_f03\" class=\"figure large editable block\">\n<div style=\"width: 1769px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/20164802\/1e8b019bfe6949342d49dc98e9c1335f.jpg\" alt=\"image\" width=\"1759\" height=\"807\" \/><\/p>\n<p class=\"wp-caption-text\"><em>Figure 12.3 Members of a Homologous Series.\u00a0<\/em>Each succeeding formula incorporates one carbon atom and two hydrogen atoms more than the previous formula.<\/p>\n<\/div>\n<\/div>\n<p id=\"gob-ch12_s02_p07\" class=\"para editable block\">The principle of homology allows us to write a general formula for alkanes: C<sub class=\"subscript\"><em class=\"emphasis\">n<\/em><\/sub>H<sub class=\"subscript\">2<\/sub><sub class=\"subscript\"><em class=\"emphasis\">n<\/em><\/sub> <sub class=\"subscript\">+ 2<\/sub>. Using this formula, we can write a molecular formula for any alkane with a given number of carbon atoms. For example, an alkane with eight carbon atoms has the molecular formula C<sub class=\"subscript\">8<\/sub>H<sub class=\"subscript\">(2 \u00d7 8) + 2<\/sub> = C<sub class=\"subscript\">8<\/sub>H<sub class=\"subscript\">18<\/sub>.<\/p>\n<div id=\"gob-ch12_s02_qs01\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch12_s02_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<ol id=\"gob-ch12_s02_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch12_s02_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s02_qs01_p01\" class=\"para\">In the homologous series of alkanes, what is the molecular formula for the member just above C<sub class=\"subscript\">8<\/sub>H<sub class=\"subscript\">18<\/sub>?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch12_s02_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s02_qs01_p03\" class=\"para\">Use the general formula for alkanes to write the molecular formula of the alkane with 12 carbon atoms.<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch12_s02_qs01_ans\" 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=\"q872574\">Show Answer<\/span><\/p>\n<div id=\"q872574\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li>C<sub>9<\/sub>H<sub>20<\/sub><\/li>\n<li>C<sub>12<\/sub>H<sub>26<\/sub>\u00a0<\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<div class=\"textbox key-takeaways\">\n<div id=\"gob-ch12_s02_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Key Takeaway<\/h3>\n<\/div>\n<div id=\"gob-ch12_s02_n04\" class=\"key_takeaways editable block\">\n<ul id=\"gob-ch12_s02_l03\" class=\"itemizedlist\">\n<li>Simple alkanes exist as a homologous series, in which adjacent members differ by a CH<sub class=\"subscript\">2<\/sub> unit.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch12_s02_qs02\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<h3>Exercises<\/h3>\n<div id=\"book-content\">\n<div id=\"gob-ch12_s02\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch12_s02_qs02\" class=\"qandaset block\">\n<h3 class=\"title\">Exercises<\/h3>\n<ol id=\"gob-ch12_s02_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch12_s02_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s02_qs02_p01\" class=\"para\">What compounds contain fewer carbon atoms than C<sub class=\"subscript\">3<\/sub>H<sub class=\"subscript\">8<\/sub> and are its homologs?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch12_s02_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s02_qs02_p03\" class=\"para\">What compounds contain five to eight carbon atoms and are homologs of C<sub class=\"subscript\">4<\/sub>H<sub class=\"subscript\">10<\/sub>?<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch12_s02_qs02_ans\" class=\"qandaset block\">\n<h3 class=\"title\">Answer<\/h3>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q679453\">Show Answer<\/span><\/p>\n<div id=\"q679453\" class=\"hidden-answer\" style=\"display: none\">1. CH<sub>4<\/sub> and C<sub>2<\/sub>H<sub>6<\/sub> \u00a0<\/div>\n<\/div>\n<div class=\"answer\"><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p>&nbsp;<\/p>\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-957\">\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":44985,"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-957","chapter","type-chapter","status-publish","hentry"],"part":941,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/957","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/users\/44985"}],"version-history":[{"count":6,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/957\/revisions"}],"predecessor-version":[{"id":3461,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/957\/revisions\/3461"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/parts\/941"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/957\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/media?parent=957"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=957"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/contributor?post=957"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/license?post=957"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}