{"id":1526,"date":"2018-03-21T15:23:00","date_gmt":"2018-03-21T15:23:00","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/functional-groups-of-the-carboxylic-acids-and-their-derivatives\/"},"modified":"2018-05-09T16:33:12","modified_gmt":"2018-05-09T16:33:12","slug":"functional-groups-of-the-carboxylic-acids-and-their-derivatives","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/functional-groups-of-the-carboxylic-acids-and-their-derivatives\/","title":{"raw":"15.1 Functional Groups of the Carboxylic Acids and Their Derivatives","rendered":"15.1 Functional Groups of the Carboxylic Acids and Their Derivatives"},"content":{"raw":"<div id=\"book-content\">\r\n<div id=\"gob-ch15_s01\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch15_s01_n01\" class=\"learning_objectives editable block\">\r\n<div class=\"textbox learning-objectives\">\r\n<div id=\"gob-ch15_s01_n01\" class=\"learning_objectives editable block\">\r\n<h3 class=\"title\">Learning Objectives<\/h3>\r\n<ol id=\"gob-ch15_s01_l01\" class=\"orderedlist\">\r\n \t<li>Identify the general structure for a carboxylic acid, an ester, an amine, and an amide.<\/li>\r\n \t<li>Identify the functional group for a carboxylic acid, an ester, an amine, and an amide.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<p class=\"title\">We introduced the carbonyl group (C=O)\u2014the functional group of aldehydes and ketones\u2014in <a class=\"xref\" style=\"font-size: 1rem;font-weight: normal;text-align: initial\" href=\"gob-ch14#gob-ch14\">Chapter 14 \"Organic Compounds of Oxygen\"<\/a><span style=\"font-size: 1rem;font-weight: normal;text-align: initial;color: #373d3f\">. The carbonyl group is also found in carboxylic acids, esters, and amides. However, in these compounds, the carbonyl group is only <\/span><em class=\"emphasis\" style=\"font-size: 1rem;font-weight: normal;text-align: initial;color: #373d3f\">part<\/em><span style=\"font-size: 1rem;font-weight: normal;text-align: initial;color: #373d3f\"> of the functional group.<\/span><\/p>\r\n\r\n<\/div>\r\n<p id=\"gob-ch15_s01_p02\" class=\"para editable block\">A <span class=\"margin_term\"><span class=\"glossterm\">carboxylic acid<\/span><\/span>\u00a0is an organic compound that has a <span class=\"margin_term\"><span class=\"glossterm\">carboxyl group<\/span><\/span>. The carboxyl group is a functional group that contains a carbon\u2013oxygen double bond and an OH group also attached to the same carbon atom, but it has characteristic properties of its own. As with aldehydes and ketones, carboxylic acid formulas can be written to show the carbon-to-oxygen double bond explicitly, or the carboxyl group can be written in condensed form on one line. In general, carboxylic acids are represented by the formula RCOOH, where R is a hydrocarbon group.<\/p>\r\n\r\n<div class=\"informalfigure large block\"><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152232\/18e9bed0889ba0a247f38f8014c609ba.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch15_s01_p03\" class=\"para editable block\">Esters are represented by the formula RCOOR\u2019, where R and R\u2019 are hydrocarbon groups. The <span class=\"margin_term\"><span class=\"glossterm\">ester<\/span><\/span>, which is organic compound derived from a carboxylic acid and an alcohol in which the OH of the acid is replaced by an OR group, looks somewhat like an ether and also somewhat like a carboxylic acid. Even so, compounds in this group react <em class=\"emphasis\">neither<\/em> like carboxylic acids nor like ethers; they make up a distinctive family. Unlike ethers, esters have a carbonyl group. Unlike carboxylic acids, esters have no acidic hydrogen atom; they have a hydrocarbon group in its place.<\/p>\r\n\r\n<div class=\"informalfigure large block\"><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152234\/1e1a1ee745274c6d2d68c7ac20a76166.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch15_s01_p04\" class=\"para editable block\">An <span class=\"margin_term\"><span class=\"glossterm\">amine<\/span><\/span>\u00a0is a compound derived from ammonia (NH<sub class=\"subscript\">3<\/sub>); it has one, two, or all three of the hydrogen atoms of NH<sub class=\"subscript\">3<\/sub> replaced by an alkyl (or an aryl) group. Like NH<sub class=\"subscript\">3<\/sub>, amines are weak bases. The functional group of an amine is a nitrogen atom with a lone pair of electrons and with one, two, or three alkyl or aryl groups attached.<\/p>\r\n\r\n<div class=\"informalfigure large block\"><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152236\/a286001933563022095113e5ed7f83a0.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch15_s01_p05\" class=\"para editable block\">The <span class=\"margin_term\"><span class=\"glossterm\">amide<\/span><\/span>\u00a0functional group has a carbonyl group joined to a nitrogen atom from ammonia or an amine. The properties of the amide functional group differ from those of the simple carbonyl group, NH<sub class=\"subscript\">3<\/sub>, and amines.<\/p>\r\n\r\n<div class=\"informalfigure large block\"><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152239\/ba9c89c2d3358eb3e595f41540de1e1b.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch15_s01_p06\" class=\"para editable block\">Esters and amides are considered to be <em class=\"emphasis\">derivatives<\/em> of carboxylic acids because the OH in the carboxyl group is replaced with another group. These functional groups are listed in <a class=\"xref\" href=\"#gob-ch15_s01_t01\">Table 15.1 \"Organic Acids, Bases, and Acid Derivatives\"<\/a>, along with an example (identified by common and International Union of Pure and Applied Chemistry [IUPAC] names) for each type of compound.<\/p>\r\n\r\n<div id=\"gob-ch15_s01_n02\" class=\"callout editable block\">\r\n<div class=\"textbox\">\r\n<h3 class=\"title\">Note<\/h3>\r\n<p id=\"gob-ch15_s01_p07\" class=\"para\">Most familiar carboxylic acids have an even number of carbon atoms. As we shall see in <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-17\">Chapter 17 \"Lipids\"<\/a>, these acids\u2014called fatty acids\u2014are synthesized in nature by adding two carbon atoms at a time.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s01_t01\" class=\"table block\">\r\n<p class=\"title\"><span class=\"title-prefix\">Table 15.1<\/span> Organic Acids, Bases, and Acid Derivatives<\/p>\r\n\r\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\r\n<thead>\r\n<tr>\r\n<th>Family<\/th>\r\n<th>Functional Group<\/th>\r\n<th>Example<\/th>\r\n<th>Common Name<\/th>\r\n<th>IUPAC Name<\/th>\r\n<\/tr>\r\n<\/thead>\r\n<tbody>\r\n<tr>\r\n<td>carboxylic acid<\/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\/21152241\/67bbe588a84302f514a2f5e5ed88df39.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\/21152242\/9d99bc7b85fc7046eec82c8ce03086eb.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>acetic acid<\/td>\r\n<td>ethanoic acid<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>amine<\/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\/21152243\/31310f3476f37e026179d109ec047e17.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>CH<sub class=\"subscript\">3<\/sub>NH<sub class=\"subscript\">2<\/sub><\/td>\r\n<td>methylamine<\/td>\r\n<td>methanamine (aminomethane)<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>amide<\/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\/21152244\/1f32646ac4568c84e214c5ec01404f19.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\/21152245\/57d07c472b003362bb4c6a84a36dc959.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>acetamide<\/td>\r\n<td>ethanamide<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>ester<\/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\/21152246\/ad9e569f534cb5fc015d52c4931522e4.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\/21152248\/602d23be738ad503008c8e24f764af05.jpg\" alt=\"image\" \/><\/div><\/td>\r\n<td>methyl acetate<\/td>\r\n<td>methyl ethanoate<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<\/div>\r\n<div id=\"gob-ch15_s01_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch15_s01_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<ol id=\"gob-ch15_s01_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s01_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s01_qs01_p01\" class=\"para\">How is the carboxyl group related to the carbonyl group and the OH group?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s01_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s01_qs01_p03\" class=\"para\">How is the amide group related to the carboxyl group and amines?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n[reveal-answer q=\"975693\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"975693\"]\r\n<ol>\r\n \t<li>The carboxyl group has a carbonyl group joined to an OH group.<\/li>\r\n \t<li>The amide group has a carboxyl group joined to an amino group.[\/hidden-answer]\r\n<div class=\"answer\">\r\n<p id=\"gob-ch15_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>\r\n<div id=\"gob-ch15_s01_n04\" class=\"key_takeaways editable block\">\r\n<div class=\"textbox key-takeaways\">\r\n<h3 class=\"title\">Key Takeaway<\/h3>\r\n<ul id=\"gob-ch15_s01_l03\" class=\"itemizedlist\">\r\n \t<li>Knowledge of carboxylic acids, esters, amines, and amides underlies an understanding of biologically important molecules.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s01_qs02\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<h3 class=\"title\">Exercises<\/h3>\r\n<ol id=\"gob-ch15_s01_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s01_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s01_qs02_p01\" class=\"para\">Draw the functional group in each class of compounds.<\/p>\r\n\r\n<ol id=\"gob-ch15_s01_qs02_l01\" class=\"orderedlist\">\r\n \t<li>aldehydes<\/li>\r\n \t<li>esters<\/li>\r\n \t<li>carboxylic acids<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s01_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s01_qs02_p02\" class=\"para\">How are the functional groups in Exercise 1 alike and different?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s01_qs02_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s01_qs02_p04\" class=\"para\">Draw the functional group in each class of compounds.<\/p>\r\n\r\n<ol id=\"gob-ch15_s01_qs02_l03\" class=\"orderedlist\">\r\n \t<li>amides<\/li>\r\n \t<li>ketones<\/li>\r\n \t<li>ethers<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s01_qs02_qd01_qa04\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s01_qs02_p05\" class=\"para\">How are the functional groups in Exercise 2 alike and different?<\/p>\r\n\r\n<\/div>\r\n&nbsp;<\/li>\r\n<\/ol>\r\n[reveal-answer q=\"908562\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"908562\"]\r\n\r\n1. a.\u00a0<img class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152249\/6d6c9d41fee112242f0f1f64f373bd92.jpg\" alt=\"image\" \/>\r\n\r\n<span style=\"font-size: 1rem;text-align: initial\">b.<\/span><img class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152252\/c177d59d39eb776860f80faba6772de5.jpg\" alt=\"image\" \/><span style=\"font-size: 1rem;text-align: initial\">\u00a0<\/span>\r\n\r\n<span style=\"font-size: 1rem;text-align: initial\">c.\u00a0<\/span><img class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152253\/4796386907606a68d89cd111336a8cbf.jpg\" alt=\"image\" \/>\r\n\r\n<span style=\"font-size: 1rem;text-align: initial\">3. a.<\/span><img class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152255\/d144310dcd84a993d90d1ec38aeaf6ef.jpg\" alt=\"image\" \/><span style=\"font-size: 1rem;text-align: initial\">\u00a0<\/span>\r\n\r\n<span style=\"font-size: 1rem;text-align: initial\">b.<\/span><img class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152257\/03b5d6293c878f08317d7ce97f1284be.jpg\" alt=\"image\" \/>\r\n\r\n<span style=\"font-size: 1rem;text-align: initial\">c.\u00a0<\/span><img class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152259\/86ac829885c431af1db5e32e6c60005c.jpg\" alt=\"image\" \/><span style=\"font-size: 1rem;text-align: initial\">\u00a0[\/hidden-answer]<\/span>\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>","rendered":"<div id=\"book-content\">\n<div id=\"gob-ch15_s01\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch15_s01_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<div id=\"gob-ch15_s01_n01\" class=\"learning_objectives editable block\">\n<h3 class=\"title\">Learning Objectives<\/h3>\n<ol id=\"gob-ch15_s01_l01\" class=\"orderedlist\">\n<li>Identify the general structure for a carboxylic acid, an ester, an amine, and an amide.<\/li>\n<li>Identify the functional group for a carboxylic acid, an ester, an amine, and an amide.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<p class=\"title\">We introduced the carbonyl group (C=O)\u2014the functional group of aldehydes and ketones\u2014in <a class=\"xref\" style=\"font-size: 1rem;font-weight: normal;text-align: initial\" href=\"gob-ch14#gob-ch14\">Chapter 14 &#8220;Organic Compounds of Oxygen&#8221;<\/a><span style=\"font-size: 1rem;font-weight: normal;text-align: initial;color: #373d3f\">. The carbonyl group is also found in carboxylic acids, esters, and amides. However, in these compounds, the carbonyl group is only <\/span><em class=\"emphasis\" style=\"font-size: 1rem;font-weight: normal;text-align: initial;color: #373d3f\">part<\/em><span style=\"font-size: 1rem;font-weight: normal;text-align: initial;color: #373d3f\"> of the functional group.<\/span><\/p>\n<\/div>\n<p id=\"gob-ch15_s01_p02\" class=\"para editable block\">A <span class=\"margin_term\"><span class=\"glossterm\">carboxylic acid<\/span><\/span>\u00a0is an organic compound that has a <span class=\"margin_term\"><span class=\"glossterm\">carboxyl group<\/span><\/span>. The carboxyl group is a functional group that contains a carbon\u2013oxygen double bond and an OH group also attached to the same carbon atom, but it has characteristic properties of its own. As with aldehydes and ketones, carboxylic acid formulas can be written to show the carbon-to-oxygen double bond explicitly, or the carboxyl group can be written in condensed form on one line. In general, carboxylic acids are represented by the formula RCOOH, where R is a hydrocarbon group.<\/p>\n<div class=\"informalfigure large block\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152232\/18e9bed0889ba0a247f38f8014c609ba.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch15_s01_p03\" class=\"para editable block\">Esters are represented by the formula RCOOR\u2019, where R and R\u2019 are hydrocarbon groups. The <span class=\"margin_term\"><span class=\"glossterm\">ester<\/span><\/span>, which is organic compound derived from a carboxylic acid and an alcohol in which the OH of the acid is replaced by an OR group, looks somewhat like an ether and also somewhat like a carboxylic acid. Even so, compounds in this group react <em class=\"emphasis\">neither<\/em> like carboxylic acids nor like ethers; they make up a distinctive family. Unlike ethers, esters have a carbonyl group. Unlike carboxylic acids, esters have no acidic hydrogen atom; they have a hydrocarbon group in its place.<\/p>\n<div class=\"informalfigure large block\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152234\/1e1a1ee745274c6d2d68c7ac20a76166.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch15_s01_p04\" class=\"para editable block\">An <span class=\"margin_term\"><span class=\"glossterm\">amine<\/span><\/span>\u00a0is a compound derived from ammonia (NH<sub class=\"subscript\">3<\/sub>); it has one, two, or all three of the hydrogen atoms of NH<sub class=\"subscript\">3<\/sub> replaced by an alkyl (or an aryl) group. Like NH<sub class=\"subscript\">3<\/sub>, amines are weak bases. The functional group of an amine is a nitrogen atom with a lone pair of electrons and with one, two, or three alkyl or aryl groups attached.<\/p>\n<div class=\"informalfigure large block\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152236\/a286001933563022095113e5ed7f83a0.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch15_s01_p05\" class=\"para editable block\">The <span class=\"margin_term\"><span class=\"glossterm\">amide<\/span><\/span>\u00a0functional group has a carbonyl group joined to a nitrogen atom from ammonia or an amine. The properties of the amide functional group differ from those of the simple carbonyl group, NH<sub class=\"subscript\">3<\/sub>, and amines.<\/p>\n<div class=\"informalfigure large block\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152239\/ba9c89c2d3358eb3e595f41540de1e1b.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch15_s01_p06\" class=\"para editable block\">Esters and amides are considered to be <em class=\"emphasis\">derivatives<\/em> of carboxylic acids because the OH in the carboxyl group is replaced with another group. These functional groups are listed in <a class=\"xref\" href=\"#gob-ch15_s01_t01\">Table 15.1 &#8220;Organic Acids, Bases, and Acid Derivatives&#8221;<\/a>, along with an example (identified by common and International Union of Pure and Applied Chemistry [IUPAC] names) for each type of compound.<\/p>\n<div id=\"gob-ch15_s01_n02\" class=\"callout editable block\">\n<div class=\"textbox\">\n<h3 class=\"title\">Note<\/h3>\n<p id=\"gob-ch15_s01_p07\" class=\"para\">Most familiar carboxylic acids have an even number of carbon atoms. As we shall see in <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-17\">Chapter 17 &#8220;Lipids&#8221;<\/a>, these acids\u2014called fatty acids\u2014are synthesized in nature by adding two carbon atoms at a time.<\/p>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s01_t01\" class=\"table block\">\n<p class=\"title\"><span class=\"title-prefix\">Table 15.1<\/span> Organic Acids, Bases, and Acid Derivatives<\/p>\n<table style=\"border-spacing: 0px\" cellpadding=\"0\">\n<thead>\n<tr>\n<th>Family<\/th>\n<th>Functional Group<\/th>\n<th>Example<\/th>\n<th>Common Name<\/th>\n<th>IUPAC Name<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>carboxylic acid<\/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\/21152241\/67bbe588a84302f514a2f5e5ed88df39.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\/21152242\/9d99bc7b85fc7046eec82c8ce03086eb.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>acetic acid<\/td>\n<td>ethanoic acid<\/td>\n<\/tr>\n<tr>\n<td>amine<\/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\/21152243\/31310f3476f37e026179d109ec047e17.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>CH<sub class=\"subscript\">3<\/sub>NH<sub class=\"subscript\">2<\/sub><\/td>\n<td>methylamine<\/td>\n<td>methanamine (aminomethane)<\/td>\n<\/tr>\n<tr>\n<td>amide<\/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\/21152244\/1f32646ac4568c84e214c5ec01404f19.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\/21152245\/57d07c472b003362bb4c6a84a36dc959.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>acetamide<\/td>\n<td>ethanamide<\/td>\n<\/tr>\n<tr>\n<td>ester<\/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\/21152246\/ad9e569f534cb5fc015d52c4931522e4.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\/21152248\/602d23be738ad503008c8e24f764af05.jpg\" alt=\"image\" \/><\/div>\n<\/td>\n<td>methyl acetate<\/td>\n<td>methyl ethanoate<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<div id=\"gob-ch15_s01_qs01\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch15_s01_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<ol id=\"gob-ch15_s01_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s01_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s01_qs01_p01\" class=\"para\">How is the carboxyl group related to the carbonyl group and the OH group?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s01_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s01_qs01_p03\" class=\"para\">How is the amide group related to the carboxyl group and amines?<\/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=\"q975693\">Show Answer<\/span><\/p>\n<div id=\"q975693\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li>The carboxyl group has a carbonyl group joined to an OH group.<\/li>\n<li>The amide group has a carboxyl group joined to an amino group.<\/div>\n<\/div>\n<div class=\"answer\">\n<p id=\"gob-ch15_s01_qs01_p04_ans\" class=\"para\">\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s01_n04\" class=\"key_takeaways editable block\">\n<div class=\"textbox key-takeaways\">\n<h3 class=\"title\">Key Takeaway<\/h3>\n<ul id=\"gob-ch15_s01_l03\" class=\"itemizedlist\">\n<li>Knowledge of carboxylic acids, esters, amines, and amides underlies an understanding of biologically important molecules.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s01_qs02\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<h3 class=\"title\">Exercises<\/h3>\n<ol id=\"gob-ch15_s01_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s01_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s01_qs02_p01\" class=\"para\">Draw the functional group in each class of compounds.<\/p>\n<ol id=\"gob-ch15_s01_qs02_l01\" class=\"orderedlist\">\n<li>aldehydes<\/li>\n<li>esters<\/li>\n<li>carboxylic acids<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s01_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s01_qs02_p02\" class=\"para\">How are the functional groups in Exercise 1 alike and different?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s01_qs02_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s01_qs02_p04\" class=\"para\">Draw the functional group in each class of compounds.<\/p>\n<ol id=\"gob-ch15_s01_qs02_l03\" class=\"orderedlist\">\n<li>amides<\/li>\n<li>ketones<\/li>\n<li>ethers<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s01_qs02_qd01_qa04\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s01_qs02_p05\" class=\"para\">How are the functional groups in Exercise 2 alike and different?<\/p>\n<\/div>\n<p>&nbsp;<\/li>\n<\/ol>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q908562\">Show Answer<\/span><\/p>\n<div id=\"q908562\" class=\"hidden-answer\" style=\"display: none\">\n<p>1. a.\u00a0<img decoding=\"async\" class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152249\/6d6c9d41fee112242f0f1f64f373bd92.jpg\" alt=\"image\" \/><\/p>\n<p><span style=\"font-size: 1rem;text-align: initial\">b.<\/span><img decoding=\"async\" class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152252\/c177d59d39eb776860f80faba6772de5.jpg\" alt=\"image\" \/><span style=\"font-size: 1rem;text-align: initial\">\u00a0<\/span><\/p>\n<p><span style=\"font-size: 1rem;text-align: initial\">c.\u00a0<\/span><img decoding=\"async\" class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152253\/4796386907606a68d89cd111336a8cbf.jpg\" alt=\"image\" \/><\/p>\n<p><span style=\"font-size: 1rem;text-align: initial\">3. a.<\/span><img decoding=\"async\" class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152255\/d144310dcd84a993d90d1ec38aeaf6ef.jpg\" alt=\"image\" \/><span style=\"font-size: 1rem;text-align: initial\">\u00a0<\/span><\/p>\n<p><span style=\"font-size: 1rem;text-align: initial\">b.<\/span><img decoding=\"async\" class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152257\/03b5d6293c878f08317d7ce97f1284be.jpg\" alt=\"image\" \/><\/p>\n<p><span style=\"font-size: 1rem;text-align: initial\">c.\u00a0<\/span><img decoding=\"async\" class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21152259\/86ac829885c431af1db5e32e6c60005c.jpg\" alt=\"image\" \/><span style=\"font-size: 1rem;text-align: initial\">\u00a0<\/div>\n<\/div>\n<p><\/span><\/p>\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-1526\">\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 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