{"id":1706,"date":"2018-03-21T15:42:32","date_gmt":"2018-03-21T15:42:32","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/formation-of-amides\/"},"modified":"2018-11-09T15:43:54","modified_gmt":"2018-11-09T15:43:54","slug":"formation-of-amides","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/formation-of-amides\/","title":{"raw":"15.16 Formation of Amides","rendered":"15.16 Formation of Amides"},"content":{"raw":"<div id=\"book-content\">\r\n<div id=\"gob-ch15_s16\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch15_s16_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_s16_l01\" class=\"orderedlist\">\r\n \t<li>Describe the preparation procedure for amides.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<p id=\"gob-ch15_s16_p01\" class=\"para editable block\">The addition of ammonia (NH<sub class=\"subscript\">3<\/sub>) to a carboxylic acid forms an amide, but the reaction is very slow in the laboratory at room temperature. Water molecules are split out, and a bond is formed between the nitrogen atom and the carbonyl carbon atom.<\/p>\r\n\r\n<div id=\"fwk-gob-eq15_017\" class=\"informalfigure large block\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154228\/f5f09fde9efc3a0ede813d5ff6ddb03e.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch15_s16_p02\" class=\"para editable block\">In living cells, amide formation is catalyzed by enzymes. Proteins are polyamides; they are formed by joining amino acids into long chains. In proteins, the amide functional group is called a <em class=\"emphasis\">peptide bond<\/em>. (For more information about proteins, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-18\">Chapter 18 \"Amino Acids, Proteins, and Enzymes\"<\/a>, <a class=\"xref\" href=\"gob-ch18_s04#gob-ch18_s04\">Section 18.4 \"Proteins\"<\/a>.)<\/p>\r\n\r\n<div id=\"gob-ch15_s16_s01\" class=\"section\">\r\n<h2 class=\"title editable block\">Polyamides<\/h2>\r\n<p id=\"gob-ch15_s16_s01_p01\" class=\"para editable block\">Just as the reaction of a diol and a diacid forms a polyester (<a class=\"xref\" href=\"gob-ch15_s08#gob-ch15_s08\">Section 15.8 \"Preparation of Esters\"<\/a>), the reaction of a diacid and a diamine yields a <span class=\"margin_term\"><strong><span class=\"glossterm\">polyamide<\/span><\/strong><\/span>. The two difunctional monomers often employed are adipic acid and 1,6-hexanediamine. The monomers condense by splitting out water to form a new product, which is still difunctional and thus can react further to yield a polyamide polymer.<\/p>\r\n\r\n<div id=\"fwk-gob-eq15_018\" class=\"informalfigure large block\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154230\/2bff39f54849ff7ebee7ef01eef12fbb.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch15_s16_s01_p02\" class=\"para editable block\">Some polyamides are known as <em class=\"emphasis\">nylons<\/em>. Nylons are among the most widely used synthetic fibers\u2014for example, they are used in ropes, sails, carpets, clothing, tires, brushes, and parachutes. They also can be molded into blocks for use in electrical equipment, gears, bearings, and valves.<\/p>\r\n\r\n<div id=\"gob-ch15_s16_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch15_s16_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<ol id=\"gob-ch15_s16_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s16_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s16_qs01_p01\" class=\"para\">Write the condensed structural formulas and give names of the two compounds from which butanamide (CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CONH<sub class=\"subscript\">2<\/sub>) is formed.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s16_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s16_qs01_p03\" class=\"para\">Write the condensed structural formulas and names of the two compounds from which 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>CONHCH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub> is formed.<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch15_s16_qs01_ans\" class=\"qandaset block\">\r\n\r\n[reveal-answer q=\"77552\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"77552\"]\r\n\r\n1.CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>COOH (butanoic acid) and\u00a0NH<sub class=\"subscript\">3<\/sub>(ammonia)\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>CH<sub class=\"subscript\">2<\/sub>COOH (hexanoic acid) andCH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>NH<sub class=\"subscript\">2\u00a0<\/sub>(propylamine)\u00a0[\/hidden-answer]\r\n<div class=\"answer\"><\/div>\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox key-takeaways\">\r\n<div id=\"gob-ch15_s16_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Key Takeaway<\/h3>\r\n<\/div>\r\n<div id=\"gob-ch15_s16_s01_n02\" class=\"key_takeaways editable block\">\r\n<ul id=\"gob-ch15_s16_s01_l02\" class=\"itemizedlist\">\r\n \t<li>Amides are prepared by the reaction of a carboxylic acid with ammonia or an amine.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s16_qs02_ans\" class=\"qandaset block\">\r\n<div class=\"answer\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch15_s16_qs02\" class=\"qandaset block\">\r\n<h3 class=\"title\">Exercises<\/h3>\r\n<ol id=\"gob-ch15_s16_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s16_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s16_qs02_p01\" class=\"para\">Write the condensed structural formulas and names of the two compounds from which pentanamide (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 formed.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s16_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s16_qs02_p03\" class=\"para\">Write the condensed structural formulas and names of the two compounds from which CH<sub class=\"subscript\">3<\/sub>CONHCH<sub class=\"subscript\">3<\/sub> is formed.<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch15_s16_qs02_ans\" class=\"qandaset block\">\r\n\r\n[reveal-answer q=\"561337\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"561337\"]\r\n\r\n1.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(pentanoic acid) and NH<sub>3<\/sub> (ammonia)[\/hidden-answer]\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>","rendered":"<div id=\"book-content\">\n<div id=\"gob-ch15_s16\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch15_s16_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<h3 class=\"title\">Learning Objective<\/h3>\n<ol id=\"gob-ch15_s16_l01\" class=\"orderedlist\">\n<li>Describe the preparation procedure for amides.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<p id=\"gob-ch15_s16_p01\" class=\"para editable block\">The addition of ammonia (NH<sub class=\"subscript\">3<\/sub>) to a carboxylic acid forms an amide, but the reaction is very slow in the laboratory at room temperature. Water molecules are split out, and a bond is formed between the nitrogen atom and the carbonyl carbon atom.<\/p>\n<div id=\"fwk-gob-eq15_017\" class=\"informalfigure large block\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154228\/f5f09fde9efc3a0ede813d5ff6ddb03e.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch15_s16_p02\" class=\"para editable block\">In living cells, amide formation is catalyzed by enzymes. Proteins are polyamides; they are formed by joining amino acids into long chains. In proteins, the amide functional group is called a <em class=\"emphasis\">peptide bond<\/em>. (For more information about proteins, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-18\">Chapter 18 &#8220;Amino Acids, Proteins, and Enzymes&#8221;<\/a>, <a class=\"xref\" href=\"gob-ch18_s04#gob-ch18_s04\">Section 18.4 &#8220;Proteins&#8221;<\/a>.)<\/p>\n<div id=\"gob-ch15_s16_s01\" class=\"section\">\n<h2 class=\"title editable block\">Polyamides<\/h2>\n<p id=\"gob-ch15_s16_s01_p01\" class=\"para editable block\">Just as the reaction of a diol and a diacid forms a polyester (<a class=\"xref\" href=\"gob-ch15_s08#gob-ch15_s08\">Section 15.8 &#8220;Preparation of Esters&#8221;<\/a>), the reaction of a diacid and a diamine yields a <span class=\"margin_term\"><strong><span class=\"glossterm\">polyamide<\/span><\/strong><\/span>. The two difunctional monomers often employed are adipic acid and 1,6-hexanediamine. The monomers condense by splitting out water to form a new product, which is still difunctional and thus can react further to yield a polyamide polymer.<\/p>\n<div id=\"fwk-gob-eq15_018\" class=\"informalfigure large block\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21154230\/2bff39f54849ff7ebee7ef01eef12fbb.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch15_s16_s01_p02\" class=\"para editable block\">Some polyamides are known as <em class=\"emphasis\">nylons<\/em>. Nylons are among the most widely used synthetic fibers\u2014for example, they are used in ropes, sails, carpets, clothing, tires, brushes, and parachutes. They also can be molded into blocks for use in electrical equipment, gears, bearings, and valves.<\/p>\n<div id=\"gob-ch15_s16_qs01\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch15_s16_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<ol id=\"gob-ch15_s16_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s16_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s16_qs01_p01\" class=\"para\">Write the condensed structural formulas and give names of the two compounds from which butanamide (CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CONH<sub class=\"subscript\">2<\/sub>) is formed.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s16_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s16_qs01_p03\" class=\"para\">Write the condensed structural formulas and names of the two compounds from which 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>CONHCH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">3<\/sub> is formed.<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch15_s16_qs01_ans\" class=\"qandaset block\">\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q77552\">Show Answer<\/span><\/p>\n<div id=\"q77552\" class=\"hidden-answer\" style=\"display: none\">\n<p>1.CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>COOH (butanoic acid) and\u00a0NH<sub class=\"subscript\">3<\/sub>(ammonia)<\/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>CH<sub class=\"subscript\">2<\/sub>COOH (hexanoic acid) andCH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>NH<sub class=\"subscript\">2\u00a0<\/sub>(propylamine)\u00a0<\/div>\n<\/div>\n<div class=\"answer\"><\/div>\n<\/div>\n<\/div>\n<div class=\"textbox key-takeaways\">\n<div id=\"gob-ch15_s16_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Key Takeaway<\/h3>\n<\/div>\n<div id=\"gob-ch15_s16_s01_n02\" class=\"key_takeaways editable block\">\n<ul id=\"gob-ch15_s16_s01_l02\" class=\"itemizedlist\">\n<li>Amides are prepared by the reaction of a carboxylic acid with ammonia or an amine.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s16_qs02_ans\" class=\"qandaset block\">\n<div class=\"answer\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch15_s16_qs02\" class=\"qandaset block\">\n<h3 class=\"title\">Exercises<\/h3>\n<ol id=\"gob-ch15_s16_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s16_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s16_qs02_p01\" class=\"para\">Write the condensed structural formulas and names of the two compounds from which pentanamide (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 formed.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s16_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s16_qs02_p03\" class=\"para\">Write the condensed structural formulas and names of the two compounds from which CH<sub class=\"subscript\">3<\/sub>CONHCH<sub class=\"subscript\">3<\/sub> is formed.<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch15_s16_qs02_ans\" class=\"qandaset block\">\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q561337\">Show Answer<\/span><\/p>\n<div id=\"q561337\" class=\"hidden-answer\" style=\"display: none\">\n<p>1.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(pentanoic acid) and NH<sub>3<\/sub> (ammonia)<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\t\t\t <section class=\"citations-section\" role=\"contentinfo\">\n\t\t\t <h3>Candela Citations<\/h3>\n\t\t\t\t\t <div>\n\t\t\t\t\t\t <div id=\"citation-list-1706\">\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":17,"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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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-1706","chapter","type-chapter","status-publish","hentry"],"part":1500,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1706","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":8,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1706\/revisions"}],"predecessor-version":[{"id":3561,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1706\/revisions\/3561"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/parts\/1500"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1706\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/media?parent=1706"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=1706"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/contributor?post=1706"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/license?post=1706"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}