{"id":1719,"date":"2018-03-21T15:43:22","date_gmt":"2018-03-21T15:43:22","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/chemical-properties-of-amides-hydrolysis\/"},"modified":"2018-05-09T17:33:23","modified_gmt":"2018-05-09T17:33:23","slug":"chemical-properties-of-amides-hydrolysis","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/chemical-properties-of-amides-hydrolysis\/","title":{"raw":"15.17 Chemical Properties of Amides: Hydrolysis","rendered":"15.17 Chemical Properties of Amides: Hydrolysis"},"content":{"raw":"<div id=\"navbar-top\" class=\"navbar\"><\/div>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch15_s17\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch15_s17_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-ch15_s17_l01\" class=\"orderedlist\">\r\n \t<li>Identify the typical reaction that amides undergo.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<p id=\"gob-ch15_s17_p01\" class=\"para editable block\">Generally, amides resist hydrolysis in plain water, even after prolonged heating. In the presence of added acid or base, however, hydrolysis proceeds at a moderate rate. In living cells, amide hydrolysis is catalyzed by enzymes. Amide hydrolysis is illustrated in the following example:<\/p>\r\n\r\n<div id=\"fwk-gob-eq15_019\" class=\"informalfigure large block\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154302\/ba9627963c4fe3d4a529c33bcae6d2aa.jpg\" alt=\"image\" \/><\/div>\r\n<div id=\"gob-ch15_s17_n02\" class=\"callout editable block\">\r\n<div class=\"textbox\">\r\n<h3 class=\"title\">Note<\/h3>\r\n<p id=\"gob-ch15_s17_p02\" class=\"para\">Hydrolysis of an amide in acid solution actually gives a carboxylic acid and the <em class=\"emphasis\">salt<\/em> of ammonia or an amine (the ammonia or amine initially formed is neutralized by the acid). Basic hydrolysis gives a salt of the carboxylic acid and ammonia or an amine.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s17_n03\" class=\"exercises editable block\">\r\n<h3 class=\"title\">Example 17<\/h3>\r\n<p id=\"gob-ch15_s17_p03\" class=\"para\">Write the equation for the hydrolysis of each compound.<\/p>\r\n\r\n<ol id=\"gob-ch15_s17_l02\" class=\"orderedlist\">\r\n \t<li>butyramide<\/li>\r\n \t<li>benzamide<\/li>\r\n<\/ol>\r\n<p class=\"simpara\">Solution<\/p>\r\n\r\n<ol id=\"gob-ch15_s17_l03\" class=\"orderedlist\">\r\n \t<li>\r\n<p class=\"para\">The hydrolysis of a simple amide produces an organic acid and ammonia. Butyramide thus yields butyric acid and ammonia.<\/p>\r\n\r\n<div id=\"fwk-gob-eq15_020\" class=\"informalfigure large\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154305\/b20818d2d3033aa37d88b53737611b5a.jpg\" alt=\"image\" \/><\/div><\/li>\r\n \t<li>\r\n<p class=\"para\">The hydrolysis of an amide produces an organic acid and ammonia. Benzamide thus yields benzoic acid and ammonia.<\/p>\r\n\r\n<div id=\"fwk-gob-eq15_021\" class=\"informalfigure large\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154307\/a70b6c833854402870368eddfd67eea6.jpg\" alt=\"image\" \/><\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch15_s17_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<h3 class=\"title\">Skill-Building Exercise<\/h3>\r\n<p class=\"title\">Write the equation for the hydrolysis of each compound.<\/p>\r\n\r\n<ol id=\"gob-ch15_s17_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s17_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s17_qs01_p02\" class=\"para\">propionamide (propanamide)<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s17_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s17_qs01_p03\" class=\"para\">hexanamide<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s17_n05\" class=\"callout editable block\">\r\n<div class=\"textbox shaded\">\r\n<div id=\"gob-ch15_s17_n05\" class=\"callout editable block\">\r\n<h3 class=\"title\">Career Focus: Athletic Trainer<\/h3>\r\n<p id=\"gob-ch15_s17_p07\" class=\"para\">Athletic training is an allied health-care profession recognized by the American Medical Association. The athletic trainer\u2019s role is to recognize, evaluate, and provide immediate care for athletic injuries; prevent athletic injuries by taping, bandaging, and bracing vulnerable body parts; make referrals to medical doctors when necessary; and rehabilitate injured athletes. Athletic trainers work in high schools, colleges, and other organizations where athletics programs are found. Athletic trainers usually have a degree from an accredited athletic training program whose curriculum includes such basic science courses as biology, chemistry, and physics. These studies provide the necessary background for more applied courses, such as anatomy and physiology, exercise physiology, kinesiology, and nutrition. Knowledge of chemistry is necessary for understanding pharmacological and medical terminology. For example, athletic trainers must understand the action of numerous drugs, many of which are esters, amines, or amides like those mentioned in this chapter.<\/p>\r\n<p id=\"gob-ch15_s17_p08\" class=\"para\">Athletic trainers may have administrative duties, such as the responsibility for ordering supplies. They also need to be able to evaluate nutritional supplements because providing the wrong one can get an athlete banned from competition and may bring sanctions against a school. In short, the athletic trainer is responsible for the overall health and well-being of the athletes in his or her charge.<span style=\"color: #6c64ad;font-size: 1.2em;font-weight: 600\">\u00a0<\/span><\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch15_s17_n05\" class=\"callout editable block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<\/div>\r\n<div id=\"gob-ch15_s17_qs02\" class=\"qandaset block\">\r\n<ol id=\"gob-ch15_s17_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s17_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s17_qs02_p01\" class=\"para\">What are the products of the hydrolysis of an amide?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s17_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s17_qs02_p03\" class=\"para\">When the amide CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CONH<sub class=\"subscript\">2<\/sub> is hydrolyzed in an NaOH solution, the products are CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>COO<sup class=\"superscript\">\u2212<\/sup>Na<sup class=\"superscript\">+<\/sup> and NH<sub class=\"subscript\">3<\/sub>. What products are obtained when CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CONH<sub class=\"subscript\">2<\/sub> is hydrolyzed in an hydrochloric acid solution?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch15_s17_qs02_ans\" class=\"qandaset block\">\r\n\r\n[reveal-answer q=\"815818\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"815818\"]\r\n\r\n1. a carboxylic acid and ammonia or an amine\r\n\r\n2.CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>COOH and NH<sub>4<\/sub>Cl[\/hidden-answer]\r\n<div class=\"answer\"><\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s17_n07\" 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_s17_l06\" class=\"itemizedlist\">\r\n \t<li>The hydrolysis of an amide produces a carboxylic acid and ammonia or an amine.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s17_qs03_ans\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch15_s17_qs03\" class=\"qandaset block\">\r\n<h3 class=\"title\">Exercises<\/h3>\r\n<ol id=\"gob-ch15_s17_qs03_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s17_qs03_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s17_qs03_p01\" class=\"para\">Complete each equation.<\/p>\r\n\r\n<ol id=\"gob-ch15_s17_qs03_l01\" class=\"orderedlist\">\r\n \t<li>\r\n<div class=\"informalfigure large\"><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154310\/714f7fa7cbba7338309c7665a767ba22.jpg\" alt=\"image\" \/><\/div><\/li>\r\n \t<li>\r\n<div class=\"informalfigure large\"><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154312\/a992e05f2b956c3d0ba2fffb837dd7b1.jpg\" alt=\"image\" \/><\/div><\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s17_qs03_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s17_qs03_p02\" class=\"para\">Complete each equation.<\/p>\r\n\r\n<ol id=\"gob-ch15_s17_qs03_l03\" class=\"orderedlist\">\r\n \t<li>\r\n<div class=\"informalfigure large\"><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154315\/736d760b1c447a0377d4a2d582b90ff5.jpg\" alt=\"image\" \/><\/div><\/li>\r\n \t<li>\r\n<div class=\"informalfigure large\"><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154317\/eb5de9c8fb4df878487a87731b9b9ddd.jpg\" alt=\"image\" \/><\/div><\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch15_s17_qs03_ans\" class=\"qandaset block\">\r\n\r\n[reveal-answer q=\"692\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"692\"]\r\n\r\n1.\r\n<ol>\r\n \t<li style=\"list-style-type: none\">\r\n<ol>\r\n \t<li>CH<sub class=\"subscript\">3<\/sub>COOH + NH<sub class=\"subscript\">3<\/sub><\/li>\r\n \t<li><img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154320\/2d3591656e05634ba3254aede60544c7.jpg\" alt=\"image\" \/>[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"navbar-bottom\" class=\"navbar\"><\/div>","rendered":"<div id=\"navbar-top\" class=\"navbar\"><\/div>\n<div id=\"book-content\">\n<div id=\"gob-ch15_s17\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch15_s17_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<h3 class=\"title\">Learning Objective<\/h3>\n<ol id=\"gob-ch15_s17_l01\" class=\"orderedlist\">\n<li>Identify the typical reaction that amides undergo.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<p id=\"gob-ch15_s17_p01\" class=\"para editable block\">Generally, amides resist hydrolysis in plain water, even after prolonged heating. In the presence of added acid or base, however, hydrolysis proceeds at a moderate rate. In living cells, amide hydrolysis is catalyzed by enzymes. Amide hydrolysis is illustrated in the following example:<\/p>\n<div id=\"fwk-gob-eq15_019\" class=\"informalfigure large block\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154302\/ba9627963c4fe3d4a529c33bcae6d2aa.jpg\" alt=\"image\" \/><\/div>\n<div id=\"gob-ch15_s17_n02\" class=\"callout editable block\">\n<div class=\"textbox\">\n<h3 class=\"title\">Note<\/h3>\n<p id=\"gob-ch15_s17_p02\" class=\"para\">Hydrolysis of an amide in acid solution actually gives a carboxylic acid and the <em class=\"emphasis\">salt<\/em> of ammonia or an amine (the ammonia or amine initially formed is neutralized by the acid). Basic hydrolysis gives a salt of the carboxylic acid and ammonia or an amine.<\/p>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s17_n03\" class=\"exercises editable block\">\n<h3 class=\"title\">Example 17<\/h3>\n<p id=\"gob-ch15_s17_p03\" class=\"para\">Write the equation for the hydrolysis of each compound.<\/p>\n<ol id=\"gob-ch15_s17_l02\" class=\"orderedlist\">\n<li>butyramide<\/li>\n<li>benzamide<\/li>\n<\/ol>\n<p class=\"simpara\">Solution<\/p>\n<ol id=\"gob-ch15_s17_l03\" class=\"orderedlist\">\n<li>\n<p class=\"para\">The hydrolysis of a simple amide produces an organic acid and ammonia. Butyramide thus yields butyric acid and ammonia.<\/p>\n<div id=\"fwk-gob-eq15_020\" class=\"informalfigure large\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154305\/b20818d2d3033aa37d88b53737611b5a.jpg\" alt=\"image\" \/><\/div>\n<\/li>\n<li>\n<p class=\"para\">The hydrolysis of an amide produces an organic acid and ammonia. Benzamide thus yields benzoic acid and ammonia.<\/p>\n<div id=\"fwk-gob-eq15_021\" class=\"informalfigure large\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154307\/a70b6c833854402870368eddfd67eea6.jpg\" alt=\"image\" \/><\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch15_s17_qs01\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<h3 class=\"title\">Skill-Building Exercise<\/h3>\n<p class=\"title\">Write the equation for the hydrolysis of each compound.<\/p>\n<ol id=\"gob-ch15_s17_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s17_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s17_qs01_p02\" class=\"para\">propionamide (propanamide)<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s17_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s17_qs01_p03\" class=\"para\">hexanamide<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s17_n05\" class=\"callout editable block\">\n<div class=\"textbox shaded\">\n<div id=\"gob-ch15_s17_n05\" class=\"callout editable block\">\n<h3 class=\"title\">Career Focus: Athletic Trainer<\/h3>\n<p id=\"gob-ch15_s17_p07\" class=\"para\">Athletic training is an allied health-care profession recognized by the American Medical Association. The athletic trainer\u2019s role is to recognize, evaluate, and provide immediate care for athletic injuries; prevent athletic injuries by taping, bandaging, and bracing vulnerable body parts; make referrals to medical doctors when necessary; and rehabilitate injured athletes. Athletic trainers work in high schools, colleges, and other organizations where athletics programs are found. Athletic trainers usually have a degree from an accredited athletic training program whose curriculum includes such basic science courses as biology, chemistry, and physics. These studies provide the necessary background for more applied courses, such as anatomy and physiology, exercise physiology, kinesiology, and nutrition. Knowledge of chemistry is necessary for understanding pharmacological and medical terminology. For example, athletic trainers must understand the action of numerous drugs, many of which are esters, amines, or amides like those mentioned in this chapter.<\/p>\n<p id=\"gob-ch15_s17_p08\" class=\"para\">Athletic trainers may have administrative duties, such as the responsibility for ordering supplies. They also need to be able to evaluate nutritional supplements because providing the wrong one can get an athlete banned from competition and may bring sanctions against a school. In short, the athletic trainer is responsible for the overall health and well-being of the athletes in his or her charge.<span style=\"color: #6c64ad;font-size: 1.2em;font-weight: 600\">\u00a0<\/span><\/p>\n<\/div>\n<\/div>\n<div class=\"textbox exercises\">\n<div id=\"gob-ch15_s17_n05\" class=\"callout editable block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<\/div>\n<div id=\"gob-ch15_s17_qs02\" class=\"qandaset block\">\n<ol id=\"gob-ch15_s17_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s17_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s17_qs02_p01\" class=\"para\">What are the products of the hydrolysis of an amide?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s17_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s17_qs02_p03\" class=\"para\">When the amide CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CONH<sub class=\"subscript\">2<\/sub> is hydrolyzed in an NaOH solution, the products are CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>COO<sup class=\"superscript\">\u2212<\/sup>Na<sup class=\"superscript\">+<\/sup> and NH<sub class=\"subscript\">3<\/sub>. What products are obtained when CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CONH<sub class=\"subscript\">2<\/sub> is hydrolyzed in an hydrochloric acid solution?<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch15_s17_qs02_ans\" class=\"qandaset block\">\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q815818\">Show Answer<\/span><\/p>\n<div id=\"q815818\" class=\"hidden-answer\" style=\"display: none\">\n<p>1. a carboxylic acid and ammonia or an amine<\/p>\n<p>2.CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>COOH and NH<sub>4<\/sub>Cl<\/div>\n<\/div>\n<div class=\"answer\"><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s17_n07\" class=\"key_takeaways editable block\">\n<div class=\"textbox key-takeaways\">\n<h3 class=\"title\">Key Takeaway<\/h3>\n<ul id=\"gob-ch15_s17_l06\" class=\"itemizedlist\">\n<li>The hydrolysis of an amide produces a carboxylic acid and ammonia or an amine.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s17_qs03_ans\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch15_s17_qs03\" class=\"qandaset block\">\n<h3 class=\"title\">Exercises<\/h3>\n<ol id=\"gob-ch15_s17_qs03_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s17_qs03_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s17_qs03_p01\" class=\"para\">Complete each equation.<\/p>\n<ol id=\"gob-ch15_s17_qs03_l01\" class=\"orderedlist\">\n<li>\n<div class=\"informalfigure large\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154310\/714f7fa7cbba7338309c7665a767ba22.jpg\" alt=\"image\" \/><\/div>\n<\/li>\n<li>\n<div class=\"informalfigure large\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154312\/a992e05f2b956c3d0ba2fffb837dd7b1.jpg\" alt=\"image\" \/><\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s17_qs03_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s17_qs03_p02\" class=\"para\">Complete each equation.<\/p>\n<ol id=\"gob-ch15_s17_qs03_l03\" class=\"orderedlist\">\n<li>\n<div class=\"informalfigure large\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154315\/736d760b1c447a0377d4a2d582b90ff5.jpg\" alt=\"image\" \/><\/div>\n<\/li>\n<li>\n<div class=\"informalfigure large\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154317\/eb5de9c8fb4df878487a87731b9b9ddd.jpg\" alt=\"image\" \/><\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch15_s17_qs03_ans\" class=\"qandaset block\">\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q692\">Show Answer<\/span><\/p>\n<div id=\"q692\" class=\"hidden-answer\" style=\"display: none\">\n<p>1.<\/p>\n<ol>\n<li style=\"list-style-type: none\">\n<ol>\n<li>CH<sub class=\"subscript\">3<\/sub>COOH + NH<sub class=\"subscript\">3<\/sub><\/li>\n<li><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154320\/2d3591656e05634ba3254aede60544c7.jpg\" alt=\"image\" \/><\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"navbar-bottom\" class=\"navbar\"><\/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-1719\">\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":18,"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 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