{"id":1301,"date":"2018-03-21T14:57:27","date_gmt":"2018-03-21T14:57:27","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/organic-compounds-with-functional-groups\/"},"modified":"2018-10-30T15:48:15","modified_gmt":"2018-10-30T15:48:15","slug":"organic-compounds-with-functional-groups","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/organic-compounds-with-functional-groups\/","title":{"raw":"14.1 Organic Compounds with Functional Groups","rendered":"14.1 Organic Compounds with Functional Groups"},"content":{"raw":"<div id=\"navbar-top\" class=\"navbar\"><\/div>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch14_s01\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch14_s01_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-ch14_s01_l01\" class=\"orderedlist\">\r\n \t<li>Describe functional groups and explain why they are useful in the study of organic chemistry.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<p id=\"gob-ch14_s01_p01\" class=\"para editable block\"><a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-12\">Chapter 12 \"Organic Chemistry: Alkanes and Halogenated Hydrocarbons\"<\/a> and <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-13\">Chapter 13 \"Unsaturated and Aromatic Hydrocarbons\"\u00a0<\/a>considered several kinds of hydrocarbons, but many organic compounds contain atoms other than carbon and hydrogen in their functional groups. A <strong><span class=\"margin_term\"><span class=\"glossterm\">functional group is<\/span><\/span> a specific structural arrangement of atoms or bonds that imparts a characteristic chemical reactivity<\/strong> to the molecule.\u00a0 Understanding the behavior of a particular functional group allows prediction of chemical and physical properties of a variety of molecules, including biomolecules, that contain that particular functional group.\u00a0 In this chapter and <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-15\">Chapter 15 \"Organic Acids and Bases and Some of Their Derivatives\"<\/a>, we make a brief yet systematic study of some of organic compound families. Each family is based on a common, simple functional group that contains an oxygen atom or a nitrogen atom. Some common functional groups are listed in <a class=\"xref\" href=\"#gob-ch14_s01_t01\">Table 14.1 \"Selected Organic Functional Groups\"<\/a>.<\/p>\r\n\r\n<div id=\"gob-ch14_s01_t01\" class=\"table block\">\r\n<p class=\"title\"><span class=\"title-prefix\">Table 14.1<\/span> Selected Organic Functional Groups.\u00a0 Note that R is usually a hydrocarbon chain.\u00a0 Cases where R can be an H atom are noted.<\/p>\r\n\r\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\r\n<thead>\r\n<tr>\r\n<th>Name of Family<\/th>\r\n<th align=\"center\">General Formula<\/th>\r\n<th>Functional Group<\/th>\r\n<th>Suffix*<\/th>\r\n<\/tr>\r\n<\/thead>\r\n<tbody>\r\n<tr>\r\n<td>alkane<\/td>\r\n<td align=\"center\">RH<\/td>\r\n<td>none<\/td>\r\n<td>-<em class=\"emphasis\">ane<\/em><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>alkene<\/td>\r\n<td align=\"center\">R<sub class=\"subscript\">2<\/sub>C=CR<sub class=\"subscript\">2<\/sub>\r\n\r\nThe R groups can be Hs.<\/td>\r\n<td>\r\n<div class=\"informalfigure small\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145720\/ba65a60cebc7f5b56c0196b97a8faf04.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>-<em class=\"emphasis\">ene<\/em><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>alkyne<\/td>\r\n<td align=\"center\">RC\u2261CR\u00a0 The R groups can be Hs.<\/td>\r\n<td>\u2013C\u2261C\u2013<\/td>\r\n<td>-<em class=\"emphasis\">yne<\/em><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>alcohol<\/td>\r\n<td align=\"center\">ROH<\/td>\r\n<td>\u2013OH<\/td>\r\n<td>-<em class=\"emphasis\">ol<\/em><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>thiol<\/td>\r\n<td align=\"center\">RSH<\/td>\r\n<td>\u2013SH<\/td>\r\n<td>-<em class=\"emphasis\">thiol<\/em><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>ether<\/td>\r\n<td align=\"center\">ROR<\/td>\r\n<td>\u2013O\u2013<\/td>\r\n<td>ether<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>aldehyde<\/td>\r\n<td align=\"center\">\r\n<div class=\"informalfigure small\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145721\/6edd11b9ad9b08fe020e2622891f4a5f.jpg\" alt=\"image\" \/><\/div>\r\n<div>The R group can be H.<\/div><\/td>\r\n<td>\r\n<div class=\"informalfigure small\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145722\/05915cbbe7f39cea621c1cc3e14c6f47.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>-<em class=\"emphasis\">al<\/em><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>ketone<\/td>\r\n<td align=\"center\">\r\n<div class=\"informalfigure small\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145723\/ca175216dec283789054fea218b7f6c3.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>\r\n<div class=\"informalfigure small\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145724\/4d28b4516f31978c40f6d2de8bbf3c37.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>-<em class=\"emphasis\">one<\/em><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>carboxylic acid<\/td>\r\n<td align=\"center\">\r\n<div class=\"informalfigure small\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145725\/eb986810d5a353b5887ff8f9023caa0e.jpg\" alt=\"image\" \/><\/div>\r\n<div>The R group can be H.<\/div><\/td>\r\n<td>\r\n<div class=\"informalfigure small\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145726\/651a5e6e4014608f38132c82112717f3.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>-<em class=\"emphasis\">oic acid<\/em><\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<tfoot>\r\n<tr>\r\n<th colspan=\"4\">*Ethers do not have a suffix in their common name; all ethers end with the word <em class=\"emphasis\">ether<\/em>.<\/th>\r\n<\/tr>\r\n<\/tfoot>\r\n<\/table>\r\n<\/div>\r\n<div id=\"gob-ch14_s01_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch14_s01_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<ol id=\"gob-ch14_s01_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch14_s01_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s01_qs01_p01\" class=\"para\">What is the functional group of an alkene? An alkyne?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch14_s01_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s01_qs01_p03\" class=\"para\">Does 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\">2<\/sub>CH<sub class=\"subscript\">3<\/sub> have a functional group? Explain.<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n[reveal-answer q=\"971552\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"971552\"]\r\n<ol>\r\n \t<li>carbon-to-carbon double bond; carbon-to-carbon triple bond<\/li>\r\n \t<li>No; it has nothing but carbon and hydrogen atoms and all single bonds.[\/hidden-answer]\r\n<div class=\"answer\">\r\n<p id=\"gob-ch14_s01_qs01_p04_ans\" class=\"para\"><\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox key-takeaways\">\r\n<div id=\"gob-ch14_s01_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Key Takeaway<\/h3>\r\n<\/div>\r\n<div id=\"gob-ch14_s01_n03\" class=\"key_takeaways editable block\">\r\n<ul id=\"gob-ch14_s01_l03\" class=\"itemizedlist\">\r\n \t<li>The functional group, a structural arrangement of atoms and\/or bonds, is largely responsible for the properties of organic compound families.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch14_s01_qs02\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<h3>Exercises<\/h3>\r\n<div id=\"gob-ch14_s01_qs02\" class=\"qandaset block\">\r\n<ol id=\"gob-ch14_s01_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch14_s01_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s01_qs02_p01\" class=\"para\">What is the functional group of 1-butanol (CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>OH)?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch14_s01_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s01_qs02_p03\" class=\"para\">What is the functional group of butyl bromide, CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>Br?<\/p>\r\n<p class=\"para\">[reveal-answer q=\"257935\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"257935\"]1. OH\u00a0[\/hidden-answer]<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch14_s01_qs02_ans\" class=\"qandaset block\"><\/div>\r\n<\/div>\r\n<\/div>","rendered":"<div id=\"navbar-top\" class=\"navbar\"><\/div>\n<div id=\"book-content\">\n<div id=\"gob-ch14_s01\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch14_s01_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<h3 class=\"title\">Learning Objective<\/h3>\n<ol id=\"gob-ch14_s01_l01\" class=\"orderedlist\">\n<li>Describe functional groups and explain why they are useful in the study of organic chemistry.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<p id=\"gob-ch14_s01_p01\" class=\"para editable block\"><a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-12\">Chapter 12 &#8220;Organic Chemistry: Alkanes and Halogenated Hydrocarbons&#8221;<\/a> and <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-13\">Chapter 13 &#8220;Unsaturated and Aromatic Hydrocarbons&#8221;\u00a0<\/a>considered several kinds of hydrocarbons, but many organic compounds contain atoms other than carbon and hydrogen in their functional groups. A <strong><span class=\"margin_term\"><span class=\"glossterm\">functional group is<\/span><\/span> a specific structural arrangement of atoms or bonds that imparts a characteristic chemical reactivity<\/strong> to the molecule.\u00a0 Understanding the behavior of a particular functional group allows prediction of chemical and physical properties of a variety of molecules, including biomolecules, that contain that particular functional group.\u00a0 In this chapter and <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-15\">Chapter 15 &#8220;Organic Acids and Bases and Some of Their Derivatives&#8221;<\/a>, we make a brief yet systematic study of some of organic compound families. Each family is based on a common, simple functional group that contains an oxygen atom or a nitrogen atom. Some common functional groups are listed in <a class=\"xref\" href=\"#gob-ch14_s01_t01\">Table 14.1 &#8220;Selected Organic Functional Groups&#8221;<\/a>.<\/p>\n<div id=\"gob-ch14_s01_t01\" class=\"table block\">\n<p class=\"title\"><span class=\"title-prefix\">Table 14.1<\/span> Selected Organic Functional Groups.\u00a0 Note that R is usually a hydrocarbon chain.\u00a0 Cases where R can be an H atom are noted.<\/p>\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\n<thead>\n<tr>\n<th>Name of Family<\/th>\n<th align=\"center\">General Formula<\/th>\n<th>Functional Group<\/th>\n<th>Suffix*<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>alkane<\/td>\n<td align=\"center\">RH<\/td>\n<td>none<\/td>\n<td>&#8211;<em class=\"emphasis\">ane<\/em><\/td>\n<\/tr>\n<tr>\n<td>alkene<\/td>\n<td align=\"center\">R<sub class=\"subscript\">2<\/sub>C=CR<sub class=\"subscript\">2<\/sub><\/p>\n<p>The R groups can be Hs.<\/td>\n<td>\n<div class=\"informalfigure small\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145720\/ba65a60cebc7f5b56c0196b97a8faf04.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>&#8211;<em class=\"emphasis\">ene<\/em><\/td>\n<\/tr>\n<tr>\n<td>alkyne<\/td>\n<td align=\"center\">RC\u2261CR\u00a0 The R groups can be Hs.<\/td>\n<td>\u2013C\u2261C\u2013<\/td>\n<td>&#8211;<em class=\"emphasis\">yne<\/em><\/td>\n<\/tr>\n<tr>\n<td>alcohol<\/td>\n<td align=\"center\">ROH<\/td>\n<td>\u2013OH<\/td>\n<td>&#8211;<em class=\"emphasis\">ol<\/em><\/td>\n<\/tr>\n<tr>\n<td>thiol<\/td>\n<td align=\"center\">RSH<\/td>\n<td>\u2013SH<\/td>\n<td>&#8211;<em class=\"emphasis\">thiol<\/em><\/td>\n<\/tr>\n<tr>\n<td>ether<\/td>\n<td align=\"center\">ROR<\/td>\n<td>\u2013O\u2013<\/td>\n<td>ether<\/td>\n<\/tr>\n<tr>\n<td>aldehyde<\/td>\n<td align=\"center\">\n<div class=\"informalfigure small\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145721\/6edd11b9ad9b08fe020e2622891f4a5f.jpg\" alt=\"image\" \/><\/div>\n<div>The R group can be H.<\/div>\n<\/td>\n<td>\n<div class=\"informalfigure small\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145722\/05915cbbe7f39cea621c1cc3e14c6f47.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>&#8211;<em class=\"emphasis\">al<\/em><\/td>\n<\/tr>\n<tr>\n<td>ketone<\/td>\n<td align=\"center\">\n<div class=\"informalfigure small\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145723\/ca175216dec283789054fea218b7f6c3.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>\n<div class=\"informalfigure small\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145724\/4d28b4516f31978c40f6d2de8bbf3c37.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>&#8211;<em class=\"emphasis\">one<\/em><\/td>\n<\/tr>\n<tr>\n<td>carboxylic acid<\/td>\n<td align=\"center\">\n<div class=\"informalfigure small\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145725\/eb986810d5a353b5887ff8f9023caa0e.jpg\" alt=\"image\" \/><\/div>\n<div>The R group can be H.<\/div>\n<\/td>\n<td>\n<div class=\"informalfigure small\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21145726\/651a5e6e4014608f38132c82112717f3.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>&#8211;<em class=\"emphasis\">oic acid<\/em><\/td>\n<\/tr>\n<\/tbody>\n<tfoot>\n<tr>\n<th colspan=\"4\">*Ethers do not have a suffix in their common name; all ethers end with the word <em class=\"emphasis\">ether<\/em>.<\/th>\n<\/tr>\n<\/tfoot>\n<\/table>\n<\/div>\n<div id=\"gob-ch14_s01_qs01\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch14_s01_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<ol id=\"gob-ch14_s01_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch14_s01_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s01_qs01_p01\" class=\"para\">What is the functional group of an alkene? An alkyne?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch14_s01_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s01_qs01_p03\" class=\"para\">Does 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\">2<\/sub>CH<sub class=\"subscript\">3<\/sub> have a functional group? Explain.<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q971552\">Show Answer<\/span><\/p>\n<div id=\"q971552\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li>carbon-to-carbon double bond; carbon-to-carbon triple bond<\/li>\n<li>No; it has nothing but carbon and hydrogen atoms and all single bonds.<\/div>\n<\/div>\n<div class=\"answer\">\n<p id=\"gob-ch14_s01_qs01_p04_ans\" class=\"para\">\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<div class=\"textbox key-takeaways\">\n<div id=\"gob-ch14_s01_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Key Takeaway<\/h3>\n<\/div>\n<div id=\"gob-ch14_s01_n03\" class=\"key_takeaways editable block\">\n<ul id=\"gob-ch14_s01_l03\" class=\"itemizedlist\">\n<li>The functional group, a structural arrangement of atoms and\/or bonds, is largely responsible for the properties of organic compound families.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch14_s01_qs02\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<h3>Exercises<\/h3>\n<div id=\"gob-ch14_s01_qs02\" class=\"qandaset block\">\n<ol id=\"gob-ch14_s01_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch14_s01_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s01_qs02_p01\" class=\"para\">What is the functional group of 1-butanol (CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>OH)?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch14_s01_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s01_qs02_p03\" class=\"para\">What is the functional group of butyl bromide, CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>Br?<\/p>\n<p class=\"para\">\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q257935\">Show Answer<\/span><\/p>\n<div id=\"q257935\" class=\"hidden-answer\" style=\"display: none\">1. OH\u00a0<\/div>\n<\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch14_s01_qs02_ans\" class=\"qandaset block\"><\/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-1301\">\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":53384,"menu_order":2,"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-1301","chapter","type-chapter","status-publish","hentry"],"part":1285,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1301","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\/53384"}],"version-history":[{"count":11,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1301\/revisions"}],"predecessor-version":[{"id":3507,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1301\/revisions\/3507"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/parts\/1285"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1301\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/media?parent=1301"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=1301"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/contributor?post=1301"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/license?post=1301"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}