{"id":1035,"date":"2018-03-20T16:55:55","date_gmt":"2018-03-20T16:55:55","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/?post_type=chapter&#038;p=1035"},"modified":"2018-03-29T16:29:43","modified_gmt":"2018-03-29T16:29:43","slug":"12-7-chemical-properties-of-alkanes","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/12-7-chemical-properties-of-alkanes\/","title":{"raw":"12.7 Chemical Properties of Alkanes","rendered":"12.7 Chemical Properties of Alkanes"},"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-ch12_s07\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch12_s07_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-ch12_s07_l01\" class=\"orderedlist\">\r\n \t<li>Identify the main chemical properties of alkanes.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<span style=\"font-size: 1rem;text-align: initial\">Alkane molecules are nonpolar and therefore generally do not react with ionic compounds such as most laboratory acids, bases, oxidizing agents, or reducing agents. Consider butane as an example:<\/span>\r\n\r\n<\/div>\r\n<div id=\"fwk-gob-eq12_001\" class=\"informalfigure large block\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/20165524\/66dc60cbec61ff3a93f93302145b5a72.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch12_s07_p02\" class=\"para editable block\">Neither positive ions nor negative ions are attracted to a nonpolar molecule. In fact, the alkanes undergo so few reactions that they are sometimes called <em class=\"emphasis\">paraffins<\/em>, from the Latin <em class=\"emphasis\">parum affinis<\/em>, meaning \u201clittle affinity.\u201d<\/p>\r\n<p id=\"gob-ch12_s07_p03\" class=\"para editable block\">Two important reactions that the alkanes do undergo are combustion and halogenation. Nothing happens when alkanes are merely mixed with oxygen (O<sub class=\"subscript\">2<\/sub>) at room temperature, but when a flame or spark provides the activation energy, a highly exothermic <span class=\"margin_term\"><strong><span class=\"glossterm\">combustion reaction<\/span><\/strong><\/span>\u00a0proceeds vigorously. For methane (CH<sub class=\"subscript\">4<\/sub>), the reaction is as follows:<\/p>\r\n<span class=\"informalequation block\"><span class=\"mathphrase\">CH<sub class=\"subscript\">4<\/sub> + 2O<sub class=\"subscript\">2<\/sub> \u2192 CO<sub class=\"subscript\">2<\/sub> + 2H<sub class=\"subscript\">2<\/sub>O + heat<\/span><\/span>\r\n<p id=\"gob-ch12_s07_p04\" class=\"para editable block\">If the reactants are adequately mixed and there is sufficient oxygen, the only products are carbon dioxide (CO<sub class=\"subscript\">2<\/sub>), water (H<sub class=\"subscript\">2<\/sub>O), and heat\u2014heat for cooking foods, heating homes, and drying clothes. Because conditions are rarely ideal, however, other products are frequently formed. When the oxygen supply is limited, carbon monoxide (CO) is a by-product:<\/p>\r\n<span class=\"informalequation block\"><span class=\"mathphrase\">2CH<sub class=\"subscript\">4<\/sub> + 3O<sub class=\"subscript\">2<\/sub> \u2192 2CO + 4H<sub class=\"subscript\">2<\/sub>O<\/span><\/span>\r\n<p id=\"gob-ch12_s07_p05\" class=\"para editable block\">This reaction is responsible for dozens of deaths each year from unventilated or improperly adjusted gas heaters. (Similar reactions with similar results occur with kerosene heaters.)<\/p>\r\n<p id=\"gob-ch12_s07_p06\" class=\"para editable block\">Alkanes also react with the halogens chlorine (Cl<sub class=\"subscript\">2<\/sub>) and bromine (Br<sub class=\"subscript\">2<\/sub>) in the presence of ultraviolet light or at high temperatures to yield chlorinated and brominated alkanes. For example, chlorine reacts with excess methane (CH<sub class=\"subscript\">4<\/sub>) to give methyl chloride (CH<sub class=\"subscript\">3<\/sub>Cl).<\/p>\r\n<span class=\"informalequation block\"><span class=\"mathphrase\">CH<sub class=\"subscript\">4<\/sub> + Cl<sub class=\"subscript\">2<\/sub> \u2192 CH<sub class=\"subscript\">3<\/sub>Cl + HCl<\/span><\/span>\r\n<p id=\"gob-ch12_s07_p07\" class=\"para editable block\">With more chlorine, a mixture of products is obtained: CH<sub class=\"subscript\">3<\/sub>Cl, CH<sub class=\"subscript\">2<\/sub>Cl<sub class=\"subscript\">2<\/sub>, CHCl<sub class=\"subscript\">3<\/sub>, and CCl<sub class=\"subscript\">4<\/sub>.<\/p>\r\n<p id=\"gob-ch12_s07_p08\" class=\"para editable block\">Fluorine (F<sub class=\"subscript\">2<\/sub>), the lightest halogen, combines explosively with most hydrocarbons. Iodine (I<sub class=\"subscript\">2<\/sub>) is relatively unreactive. Fluorinated and iodinated alkanes are produced by indirect methods. We will discuss the names and uses of halogenated hydrocarbons in Section 12.8 \"Halogenated Hydrocarbons\".<\/p>\r\n\r\n<div id=\"gob-ch12_s07_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch12_s07_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<ol id=\"gob-ch12_s07_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch12_s07_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s07_qs01_p01\" class=\"para\">Why are alkanes sometimes called paraffins?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch12_s07_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s07_qs01_p03\" class=\"para\">Which halogen reacts most readily with alkanes? Which reacts least readily?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch12_s07_qs01_ans\" class=\"qandaset block\">\r\n<h3 class=\"title\">Answers<\/h3>\r\n[reveal-answer q=\"214895\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"214895\"]\r\n<ol>\r\n \t<li>Alkanes do not react with many common chemicals. They are sometimes called paraffins, from the Latin parum affinis, meaning \u201clittle affinity.\u201d<\/li>\r\n \t<li>most readily: F2; least readily: I2[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch12_s07_n03\" 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-ch12_s07_l03\" class=\"itemizedlist\">\r\n \t<li>Alkanes react with oxygen (combustion) and with halogens (halogenation).<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch12_s07_qs02\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch12_s07\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch12_s07_qs02\" class=\"qandaset block\">\r\n<h3 class=\"title\">Exercises<\/h3>\r\n<ol id=\"gob-ch12_s07_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch12_s07_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s07_qs02_p01\" class=\"para\">Why do alkanes usually not react with ionic compounds such as most laboratory acids, bases, oxidizing agents, or reducing agents?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch12_s07_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s07_qs02_p03\" class=\"para\">Write an equation for the complete combustion of methane (CH<sub class=\"subscript\">4<\/sub>, the main component of natural gas).<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch12_s07_qs02_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s07_qs02_p05\" class=\"para\">What is the most important reaction of alkanes?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch12_s07_qs02_qd01_qa04\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch12_s07_qs02_p07\" class=\"para\">Name some substances other than oxygen that react readily with alkanes.<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch12_s07_qs02_ans\" class=\"qandaset block\">\r\n<h3 class=\"title\">Answers<\/h3>\r\n[reveal-answer q=\"608504\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"608504\"]\r\n\r\n1. Alkanes are nonpolar; they do not attract ions.\r\n\r\n3. combustion \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>","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-ch12_s07\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch12_s07_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<h3 class=\"title\">Learning Objective<\/h3>\n<ol id=\"gob-ch12_s07_l01\" class=\"orderedlist\">\n<li>Identify the main chemical properties of alkanes.<\/li>\n<\/ol>\n<\/div>\n<p><span style=\"font-size: 1rem;text-align: initial\">Alkane molecules are nonpolar and therefore generally do not react with ionic compounds such as most laboratory acids, bases, oxidizing agents, or reducing agents. Consider butane as an example:<\/span><\/p>\n<\/div>\n<div id=\"fwk-gob-eq12_001\" class=\"informalfigure large block\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/20165524\/66dc60cbec61ff3a93f93302145b5a72.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch12_s07_p02\" class=\"para editable block\">Neither positive ions nor negative ions are attracted to a nonpolar molecule. In fact, the alkanes undergo so few reactions that they are sometimes called <em class=\"emphasis\">paraffins<\/em>, from the Latin <em class=\"emphasis\">parum affinis<\/em>, meaning \u201clittle affinity.\u201d<\/p>\n<p id=\"gob-ch12_s07_p03\" class=\"para editable block\">Two important reactions that the alkanes do undergo are combustion and halogenation. Nothing happens when alkanes are merely mixed with oxygen (O<sub class=\"subscript\">2<\/sub>) at room temperature, but when a flame or spark provides the activation energy, a highly exothermic <span class=\"margin_term\"><strong><span class=\"glossterm\">combustion reaction<\/span><\/strong><\/span>\u00a0proceeds vigorously. For methane (CH<sub class=\"subscript\">4<\/sub>), the reaction is as follows:<\/p>\n<p><span class=\"informalequation block\"><span class=\"mathphrase\">CH<sub class=\"subscript\">4<\/sub> + 2O<sub class=\"subscript\">2<\/sub> \u2192 CO<sub class=\"subscript\">2<\/sub> + 2H<sub class=\"subscript\">2<\/sub>O + heat<\/span><\/span><\/p>\n<p id=\"gob-ch12_s07_p04\" class=\"para editable block\">If the reactants are adequately mixed and there is sufficient oxygen, the only products are carbon dioxide (CO<sub class=\"subscript\">2<\/sub>), water (H<sub class=\"subscript\">2<\/sub>O), and heat\u2014heat for cooking foods, heating homes, and drying clothes. Because conditions are rarely ideal, however, other products are frequently formed. When the oxygen supply is limited, carbon monoxide (CO) is a by-product:<\/p>\n<p><span class=\"informalequation block\"><span class=\"mathphrase\">2CH<sub class=\"subscript\">4<\/sub> + 3O<sub class=\"subscript\">2<\/sub> \u2192 2CO + 4H<sub class=\"subscript\">2<\/sub>O<\/span><\/span><\/p>\n<p id=\"gob-ch12_s07_p05\" class=\"para editable block\">This reaction is responsible for dozens of deaths each year from unventilated or improperly adjusted gas heaters. (Similar reactions with similar results occur with kerosene heaters.)<\/p>\n<p id=\"gob-ch12_s07_p06\" class=\"para editable block\">Alkanes also react with the halogens chlorine (Cl<sub class=\"subscript\">2<\/sub>) and bromine (Br<sub class=\"subscript\">2<\/sub>) in the presence of ultraviolet light or at high temperatures to yield chlorinated and brominated alkanes. For example, chlorine reacts with excess methane (CH<sub class=\"subscript\">4<\/sub>) to give methyl chloride (CH<sub class=\"subscript\">3<\/sub>Cl).<\/p>\n<p><span class=\"informalequation block\"><span class=\"mathphrase\">CH<sub class=\"subscript\">4<\/sub> + Cl<sub class=\"subscript\">2<\/sub> \u2192 CH<sub class=\"subscript\">3<\/sub>Cl + HCl<\/span><\/span><\/p>\n<p id=\"gob-ch12_s07_p07\" class=\"para editable block\">With more chlorine, a mixture of products is obtained: CH<sub class=\"subscript\">3<\/sub>Cl, CH<sub class=\"subscript\">2<\/sub>Cl<sub class=\"subscript\">2<\/sub>, CHCl<sub class=\"subscript\">3<\/sub>, and CCl<sub class=\"subscript\">4<\/sub>.<\/p>\n<p id=\"gob-ch12_s07_p08\" class=\"para editable block\">Fluorine (F<sub class=\"subscript\">2<\/sub>), the lightest halogen, combines explosively with most hydrocarbons. Iodine (I<sub class=\"subscript\">2<\/sub>) is relatively unreactive. Fluorinated and iodinated alkanes are produced by indirect methods. We will discuss the names and uses of halogenated hydrocarbons in Section 12.8 &#8220;Halogenated Hydrocarbons&#8221;.<\/p>\n<div id=\"gob-ch12_s07_qs01\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch12_s07_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<ol id=\"gob-ch12_s07_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch12_s07_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s07_qs01_p01\" class=\"para\">Why are alkanes sometimes called paraffins?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch12_s07_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s07_qs01_p03\" class=\"para\">Which halogen reacts most readily with alkanes? Which reacts least readily?<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch12_s07_qs01_ans\" class=\"qandaset block\">\n<h3 class=\"title\">Answers<\/h3>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q214895\">Show Answer<\/span><\/p>\n<div id=\"q214895\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li>Alkanes do not react with many common chemicals. They are sometimes called paraffins, from the Latin parum affinis, meaning \u201clittle affinity.\u201d<\/li>\n<li>most readily: F2; least readily: I2<\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch12_s07_n03\" class=\"key_takeaways editable block\">\n<div class=\"textbox key-takeaways\">\n<h3 class=\"title\">Key Takeaway<\/h3>\n<ul id=\"gob-ch12_s07_l03\" class=\"itemizedlist\">\n<li>Alkanes react with oxygen (combustion) and with halogens (halogenation).<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div id=\"gob-ch12_s07_qs02\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"book-content\">\n<div id=\"gob-ch12_s07\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch12_s07_qs02\" class=\"qandaset block\">\n<h3 class=\"title\">Exercises<\/h3>\n<ol id=\"gob-ch12_s07_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch12_s07_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s07_qs02_p01\" class=\"para\">Why do alkanes usually not react with ionic compounds such as most laboratory acids, bases, oxidizing agents, or reducing agents?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch12_s07_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s07_qs02_p03\" class=\"para\">Write an equation for the complete combustion of methane (CH<sub class=\"subscript\">4<\/sub>, the main component of natural gas).<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch12_s07_qs02_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s07_qs02_p05\" class=\"para\">What is the most important reaction of alkanes?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch12_s07_qs02_qd01_qa04\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch12_s07_qs02_p07\" class=\"para\">Name some substances other than oxygen that react readily with alkanes.<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch12_s07_qs02_ans\" class=\"qandaset block\">\n<h3 class=\"title\">Answers<\/h3>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q608504\">Show Answer<\/span><\/p>\n<div id=\"q608504\" class=\"hidden-answer\" style=\"display: none\">\n<p>1. Alkanes are nonpolar; they do not attract ions.<\/p>\n<p>3. combustion \u00a0<\/p><\/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-1035\">\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":44985,"menu_order":8,"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-1035","chapter","type-chapter","status-publish","hentry"],"part":941,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1035","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/wp\/v2\/users\/44985"}],"version-history":[{"count":4,"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1035\/revisions"}],"predecessor-version":[{"id":2512,"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1035\/revisions\/2512"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/pressbooks\/v2\/parts\/941"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1035\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/wp\/v2\/media?parent=1035"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=1035"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/wp\/v2\/contributor?post=1035"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/wp-json\/wp\/v2\/license?post=1035"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}