{"id":1197,"date":"2018-03-21T14:41:25","date_gmt":"2018-03-21T14:41:25","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/alkynes\/"},"modified":"2018-10-30T14:50:16","modified_gmt":"2018-10-30T14:50:16","slug":"alkynes","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/alkynes\/","title":{"raw":"13.6 Alkynes","rendered":"13.6 Alkynes"},"content":{"raw":"<div id=\"navbar-top\" class=\"navbar\">\r\n<div class=\"navbar-part left\"><\/div>\r\n<\/div>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch13_s06\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch13_s06_n01\" class=\"learning_objectives editable block\">\r\n<div class=\"textbox learning-objectives\">\r\n<h3 class=\"title\">Learning Objectives<\/h3>\r\n<ol id=\"gob-ch13_s06_l01\" class=\"orderedlist\">\r\n \t<li>Describe the general physical and chemical properties of alkynes.<\/li>\r\n \t<li>Name alkynes given formulas and write formulas for alkynes given names.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<p id=\"gob-ch13_s06_p01\" class=\"para editable block\">The simplest alkyne\u2014a hydrocarbon with carbon-to-carbon triple bond\u2014has the molecular formula C<sub class=\"subscript\">2<\/sub>H<sub class=\"subscript\">2<\/sub> and is known by its common name\u2014acetylene (<a class=\"xref\" href=\"#gob-ch13_s06_f01\">Figure 13.5 \"Ball-and-Spring Model of Acetylene\"<\/a>). Its structure is H\u2013C\u2261C\u2013H.<\/p>\r\n\r\n<div id=\"gob-ch13_s06_f01\" class=\"figure large editable block\">\r\n\r\n[caption id=\"\" align=\"aligncenter\" width=\"1545\"]<img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21144121\/a8fcc4af9afa9709d403b0501fc769f4.jpg\" alt=\"image\" width=\"1545\" height=\"465\" \/> Figure 13.5 Ball-and-Spring Model of Acetylene.\u00a0Acetylene (ethyne) is the simplest member of the alkyne family.[\/caption]\r\n<p class=\"para\"><span style=\"color: #6c64ad;font-size: 1em;font-weight: 600\">Note<\/span><\/p>\r\n\r\n<\/div>\r\n<div id=\"gob-ch13_s06_n02\" class=\"callout editable block\">\r\n<p id=\"gob-ch13_s06_p02\" class=\"para\">Acetylene is used in oxyacetylene torches for cutting and welding metals. The flame from such a torch can be very hot. Most acetylene, however, is converted to chemical intermediates that are used to make vinyl and acrylic plastics, fibers, resins, and a variety of other products.<\/p>\r\n\r\n<\/div>\r\n<p id=\"gob-ch13_s06_p03\" class=\"para editable block\">Alkynes are similar to alkenes in both physical and chemical properties. For example, alkynes undergo many of the typical addition reactions of alkenes. The International Union of Pure and Applied Chemistry (IUPAC) names for alkynes parallel those of alkenes, except that the family ending is -<em class=\"emphasis\">yne<\/em> rather than -<em class=\"emphasis\">ene<\/em>. The IUPAC name for acetylene is ethyne. The names of other alkynes are illustrated in the following exercises.<\/p>\r\n\r\n<div id=\"gob-ch13_s06_qs01_ans\" class=\"qandaset block\">\r\n<div class=\"answer\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch13_s06_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<ol id=\"gob-ch13_s06_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch13_s06_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch13_s06_qs01_p01\" class=\"para\">Briefly identify the important differences between an alkene and an alkyne. How are they similar?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch13_s06_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch13_s06_qs01_p03\" class=\"para\">The alkene (CH<sub class=\"subscript\">3<\/sub>)<sub class=\"subscript\">2<\/sub>CHCH<sub class=\"subscript\">2<\/sub>CH=CH<sub class=\"subscript\">2<\/sub> is named 4-methyl-1-pentene. What is the name of (CH<sub class=\"subscript\">3<\/sub>)<sub class=\"subscript\">2<\/sub>CHCH<sub class=\"subscript\">2<\/sub>C\u2261CH?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch13_s06_qs01_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch13_s06_qs01_p05\" class=\"para\">Do alkynes show cis-trans isomerism? Explain.<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch13_s06_qs01_ans\" class=\"qandaset block\">\r\n<div class=\"answer\">\r\n<p id=\"gob-ch13_s06_qs01_p02_ans\" class=\"para\">[reveal-answer q=\"724386\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"724386\"]<\/p>\r\n\r\n<ol>\r\n \t<li class=\"para\">Alkenes have double bonds; alkynes have triple bonds. Both undergo addition reactions.<\/li>\r\n \t<li class=\"para\">4-methyl-1-pentyne<\/li>\r\n \t<li class=\"para\">No; a triply bonded carbon atom can form only one other bond. It would have to have two groups attached to show cis-trans isomerism [\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch13_s06_n04\" class=\"key_takeaways editable block\">\r\n<div class=\"textbox key-takeaways\">\r\n<div id=\"gob-ch13_s06_n04\" class=\"key_takeaways editable block\">\r\n<h3 class=\"title\">Key Takeaway<\/h3>\r\n<ul id=\"gob-ch13_s06_l03\" class=\"itemizedlist\">\r\n \t<li>Alkynes are hydrocarbons with carbon-to-carbon triple bonds and properties much like those of alkenes.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox exercises\">\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch13_s06\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch13_s06_n04\" class=\"key_takeaways editable block\">\r\n<h3 class=\"title\">Exercises<\/h3>\r\n<\/div>\r\n<div id=\"gob-ch13_s06_qs02\" class=\"qandaset block\">\r\n<ol id=\"gob-ch13_s06_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch13_s06_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch13_s06_qs02_p01\" class=\"para\">Draw the structure for each compound.<\/p>\r\n\r\n<ol id=\"gob-ch13_s06_qs02_l01\" class=\"orderedlist\">\r\n \t<li>ethyne<\/li>\r\n \t<li>3-methyl-1-hexyne<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch13_s06_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch13_s06_qs02_p02\" class=\"para\">Draw the structure for each compound.<\/p>\r\n\r\n<ol id=\"gob-ch13_s06_qs02_l03\" class=\"orderedlist\">\r\n \t<li>4-methyl-2-hexyne<\/li>\r\n \t<li>3-octyne<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch13_s06_qs02_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch13_s06_qs02_p03\" class=\"para\">Name each alkyne.<\/p>\r\n\r\n<ol id=\"gob-ch13_s06_qs02_l05\" class=\"orderedlist\">\r\n \t<li>CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>C\u2261CH<\/li>\r\n \t<li>CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>C\u2261CCH<sub class=\"subscript\">3<\/sub><\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch13_s06_qs02_ans\" class=\"qandaset block\">\r\n\r\n[reveal-answer q=\"860158\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"860158\"]1. a. H\u2013C\u2261C\u2013H\r\n<div class=\"informalfigure large\">b.\u00a0<img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21144123\/6ab58f652a7b6776043950c2c2cfdb34.jpg\" alt=\"image\" \/><\/div>\r\n<div class=\"answer\"><\/div>\r\n<div class=\"answer\">\r\n\r\n3. a. 1-pentyne\r\n\r\nb. 2-hexyne\u00a0[\/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>\r\n<\/div>","rendered":"<div id=\"navbar-top\" class=\"navbar\">\n<div class=\"navbar-part left\"><\/div>\n<\/div>\n<div id=\"book-content\">\n<div id=\"gob-ch13_s06\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch13_s06_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<h3 class=\"title\">Learning Objectives<\/h3>\n<ol id=\"gob-ch13_s06_l01\" class=\"orderedlist\">\n<li>Describe the general physical and chemical properties of alkynes.<\/li>\n<li>Name alkynes given formulas and write formulas for alkynes given names.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<p id=\"gob-ch13_s06_p01\" class=\"para editable block\">The simplest alkyne\u2014a hydrocarbon with carbon-to-carbon triple bond\u2014has the molecular formula C<sub class=\"subscript\">2<\/sub>H<sub class=\"subscript\">2<\/sub> and is known by its common name\u2014acetylene (<a class=\"xref\" href=\"#gob-ch13_s06_f01\">Figure 13.5 &#8220;Ball-and-Spring Model of Acetylene&#8221;<\/a>). Its structure is H\u2013C\u2261C\u2013H.<\/p>\n<div id=\"gob-ch13_s06_f01\" class=\"figure large editable block\">\n<div style=\"width: 1555px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21144121\/a8fcc4af9afa9709d403b0501fc769f4.jpg\" alt=\"image\" width=\"1545\" height=\"465\" \/><\/p>\n<p class=\"wp-caption-text\">Figure 13.5 Ball-and-Spring Model of Acetylene.\u00a0Acetylene (ethyne) is the simplest member of the alkyne family.<\/p>\n<\/div>\n<p class=\"para\"><span style=\"color: #6c64ad;font-size: 1em;font-weight: 600\">Note<\/span><\/p>\n<\/div>\n<div id=\"gob-ch13_s06_n02\" class=\"callout editable block\">\n<p id=\"gob-ch13_s06_p02\" class=\"para\">Acetylene is used in oxyacetylene torches for cutting and welding metals. The flame from such a torch can be very hot. Most acetylene, however, is converted to chemical intermediates that are used to make vinyl and acrylic plastics, fibers, resins, and a variety of other products.<\/p>\n<\/div>\n<p id=\"gob-ch13_s06_p03\" class=\"para editable block\">Alkynes are similar to alkenes in both physical and chemical properties. For example, alkynes undergo many of the typical addition reactions of alkenes. The International Union of Pure and Applied Chemistry (IUPAC) names for alkynes parallel those of alkenes, except that the family ending is &#8211;<em class=\"emphasis\">yne<\/em> rather than &#8211;<em class=\"emphasis\">ene<\/em>. The IUPAC name for acetylene is ethyne. The names of other alkynes are illustrated in the following exercises.<\/p>\n<div id=\"gob-ch13_s06_qs01_ans\" class=\"qandaset block\">\n<div class=\"answer\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch13_s06_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<ol id=\"gob-ch13_s06_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch13_s06_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch13_s06_qs01_p01\" class=\"para\">Briefly identify the important differences between an alkene and an alkyne. How are they similar?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch13_s06_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch13_s06_qs01_p03\" class=\"para\">The alkene (CH<sub class=\"subscript\">3<\/sub>)<sub class=\"subscript\">2<\/sub>CHCH<sub class=\"subscript\">2<\/sub>CH=CH<sub class=\"subscript\">2<\/sub> is named 4-methyl-1-pentene. What is the name of (CH<sub class=\"subscript\">3<\/sub>)<sub class=\"subscript\">2<\/sub>CHCH<sub class=\"subscript\">2<\/sub>C\u2261CH?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch13_s06_qs01_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch13_s06_qs01_p05\" class=\"para\">Do alkynes show cis-trans isomerism? Explain.<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch13_s06_qs01_ans\" class=\"qandaset block\">\n<div class=\"answer\">\n<p id=\"gob-ch13_s06_qs01_p02_ans\" class=\"para\">\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q724386\">Show Answer<\/span><\/p>\n<div id=\"q724386\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li class=\"para\">Alkenes have double bonds; alkynes have triple bonds. Both undergo addition reactions.<\/li>\n<li class=\"para\">4-methyl-1-pentyne<\/li>\n<li class=\"para\">No; a triply bonded carbon atom can form only one other bond. It would have to have two groups attached to show cis-trans isomerism <\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch13_s06_n04\" class=\"key_takeaways editable block\">\n<div class=\"textbox key-takeaways\">\n<div id=\"gob-ch13_s06_n04\" class=\"key_takeaways editable block\">\n<h3 class=\"title\">Key Takeaway<\/h3>\n<ul id=\"gob-ch13_s06_l03\" class=\"itemizedlist\">\n<li>Alkynes are hydrocarbons with carbon-to-carbon triple bonds and properties much like those of alkenes.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div class=\"textbox exercises\">\n<div id=\"book-content\">\n<div id=\"gob-ch13_s06\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch13_s06_n04\" class=\"key_takeaways editable block\">\n<h3 class=\"title\">Exercises<\/h3>\n<\/div>\n<div id=\"gob-ch13_s06_qs02\" class=\"qandaset block\">\n<ol id=\"gob-ch13_s06_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch13_s06_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch13_s06_qs02_p01\" class=\"para\">Draw the structure for each compound.<\/p>\n<ol id=\"gob-ch13_s06_qs02_l01\" class=\"orderedlist\">\n<li>ethyne<\/li>\n<li>3-methyl-1-hexyne<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch13_s06_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch13_s06_qs02_p02\" class=\"para\">Draw the structure for each compound.<\/p>\n<ol id=\"gob-ch13_s06_qs02_l03\" class=\"orderedlist\">\n<li>4-methyl-2-hexyne<\/li>\n<li>3-octyne<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch13_s06_qs02_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch13_s06_qs02_p03\" class=\"para\">Name each alkyne.<\/p>\n<ol id=\"gob-ch13_s06_qs02_l05\" class=\"orderedlist\">\n<li>CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>C\u2261CH<\/li>\n<li>CH<sub class=\"subscript\">3<\/sub>CH<sub class=\"subscript\">2<\/sub>CH<sub class=\"subscript\">2<\/sub>C\u2261CCH<sub class=\"subscript\">3<\/sub><\/li>\n<\/ol>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch13_s06_qs02_ans\" class=\"qandaset block\">\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q860158\">Show Answer<\/span><\/p>\n<div id=\"q860158\" class=\"hidden-answer\" style=\"display: none\">1. a. H\u2013C\u2261C\u2013H<\/p>\n<div class=\"informalfigure large\">b.\u00a0<img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21144123\/6ab58f652a7b6776043950c2c2cfdb34.jpg\" alt=\"image\" \/><\/div>\n<div class=\"answer\"><\/div>\n<div class=\"answer\">\n<p>3. a. 1-pentyne<\/p>\n<p>b. 2-hexyne\u00a0<\/p><\/div>\n<\/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-1197\">\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":7,"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-1197","chapter","type-chapter","status-publish","hentry"],"part":1084,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1197","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":6,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1197\/revisions"}],"predecessor-version":[{"id":3500,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1197\/revisions\/3500"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/parts\/1084"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1197\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/media?parent=1197"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=1197"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/contributor?post=1197"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/license?post=1197"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}