{"id":1629,"date":"2018-03-21T15:34:48","date_gmt":"2018-03-21T15:34:48","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/esters-of-phosphoric-acid\/"},"modified":"2018-11-08T19:46:26","modified_gmt":"2018-11-08T19:46:26","slug":"esters-of-phosphoric-acid","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/esters-of-phosphoric-acid\/","title":{"raw":"15.10 Esters of Phosphoric Acid","rendered":"15.10 Esters of Phosphoric Acid"},"content":{"raw":"<div id=\"navbar-top\" class=\"navbar\">\r\n<div class=\"navbar-part left\">\r\n<div class=\"textbox learning-objectives\">\r\n<h3>Learning Objectives<\/h3>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch15_s10\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch15_s10_n01\" class=\"learning_objectives editable block\">\r\n<ol id=\"gob-ch15_s10_l01\" class=\"orderedlist\">\r\n \t<li>Describe phosphate esters.<\/li>\r\n \t<li>Understand why phosphate esters are important in living cells<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<span style=\"font-size: 1rem;text-align: initial\">Just as carboxylic acids do, inorganic acids such as nitric acid (HNO<\/span><sub class=\"subscript\" style=\"text-align: initial\">3<\/sub><span style=\"font-size: 1rem;text-align: initial\">), sulfuric acid (H<\/span><sub class=\"subscript\" style=\"text-align: initial\">2<\/sub><span style=\"font-size: 1rem;text-align: initial\">SO<\/span><sub class=\"subscript\" style=\"text-align: initial\">4<\/sub><span style=\"font-size: 1rem;text-align: initial\">), and phosphoric acid (H<\/span><sub class=\"subscript\" style=\"text-align: initial\">3<\/sub><span style=\"font-size: 1rem;text-align: initial\">PO<\/span><sub class=\"subscript\" style=\"text-align: initial\">4<\/sub><span style=\"font-size: 1rem;text-align: initial\">) also form esters. The esters of phosphoric acid are especially important in biochemistry. A phosphoric acid molecule can form a monoalkyl, a dialkyl, or a trialkyl ester by reaction with one, two, or three molecules of an alcohol.<\/span>\r\n\r\n<\/div>\r\n<\/div>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch15_s10\" class=\"section\" xml:lang=\"en\">\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\/21153422\/3cfccf769579de43236f74e8d70fb978.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch15_s10_p02\" class=\"para editable block\">Esters of pyrophosphoric acid and triphosphoric acid are also important in biochemistry.<\/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\/21153425\/decfc0a7b6e52e2b0572512036d0b010.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch15_s10_p03\" class=\"para editable block\">Esters of these acids are present in every plant and animal cell. They are biochemical intermediates in the transformation of food into usable energy. The bonds between phosphate units in adenosine triphosphate (ATP) are called <em class=\"emphasis\">phosphoanhydride<\/em> bonds. These are high-energy bonds that store energy from the metabolism of foods. Hydrolysis of ATP releases energy as it is needed for biochemical processes (for instance, for muscle contraction). Phosphate esters are also important structural constituents of phospholipids and nucleic acids. (For more information about phospholipids and nucleic acids, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-17\">Chapter 17 \"Lipids\"<\/a>, <a class=\"xref\" href=\"gob-ch17_s03#gob-ch17_s03\">Section 17.3 \"Membranes and Membrane Lipids\"<\/a>, and <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-19\">Chapter 19 \"Nucleic Acids\"<\/a>, respectively.)<\/p>\r\n\r\n<div id=\"gob-ch15_s10_n02\" class=\"callout block\">\r\n<div class=\"textbox\">\r\n<h3 class=\"title\">Note<\/h3>\r\n<p id=\"gob-ch15_s10_p04\" class=\"para\">The explosive nitroglycerin (glyceryl trinitrate) is an ester formed from glycerol and nitric acid. It is used in medicine to relieve chest pain in heart disease.<\/p>\r\n\r\n<\/div>\r\n<h3 class=\"title\"><img class=\"aligncenter\" style=\"color: #373d3f;font-size: 1em;font-weight: normal\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21153428\/6de233d9e5a3bd8d5a3d6b048fe409bf.jpg\" alt=\"image\" \/><\/h3>\r\n<\/div>\r\n<div id=\"gob-ch15_s10_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch15_s10_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercise<\/h3>\r\n<ol id=\"gob-ch15_s10_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s10_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s10_qs01_p01\" class=\"para\">What compounds combine to form phosphate esters?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<div id=\"gob-ch15_s10_qs01_ans\" class=\"qandaset block\">\r\n<div class=\"answer\">\r\n<p id=\"gob-ch15_s10_qs01_p02_ans\" class=\"para\">[reveal-answer q=\"577238\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"577238\"]<\/p>\r\n\r\n<ol>\r\n \t<li class=\"para\">phosphoric acids and alcohols[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s10_n04\" class=\"key_takeaways editable block\">\r\n<div class=\"textbox key-takeaways\">\r\n<h3 class=\"title\">Key Takeaways<\/h3>\r\n<ul id=\"gob-ch15_s10_l02\" class=\"itemizedlist\">\r\n \t<li>Inorganic acids such as H<sub class=\"subscript\">3<\/sub>PO<sub class=\"subscript\">4<\/sub> form esters.<\/li>\r\n \t<li>The esters of phosphoric acid are especially important in biochemistry.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch15_s10_qs02_ans\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch15_s10_qs02\" class=\"qandaset block\">\r\n<h3 class=\"title\">Exercises<\/h3>\r\n<ol id=\"gob-ch15_s10_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch15_s10_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s10_qs02_p01\" class=\"para\">Draw the structure for each compound.<\/p>\r\n\r\n<ol id=\"gob-ch15_s10_qs02_l01\" class=\"orderedlist\">\r\n \t<li>diethyl hydrogen phosphate<\/li>\r\n \t<li>methyl dihydrogen phosphate<\/li>\r\n \t<li>1-glycerol phosphate<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch15_s10_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch15_s10_qs02_p02\" class=\"para\">Name each compound.<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<div class=\"informalfigure large\">a.\u00a0<img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21153431\/8f42e2480165047bc770f077a27e00de.jpg\" alt=\"image\" \/><\/div>\r\n<div class=\"informalfigure large\">b.\u00a0<img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21153434\/71fd1300e1e4879d02e74f50b320d5a7.jpg\" alt=\"image\" \/><\/div>\r\n<div class=\"informalfigure large\">c.\u00a0<img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21153437\/3571b9501086bf1a4543b7107aa23fc2.jpg\" alt=\"image\" \/><\/div>\r\n<div>[reveal-answer q=\"434871\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"434871\"]1. a.<img src=\"https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/section_18\/0f8343077d449118a179e7e52b18ec83.jpg\" \/>b.<img src=\"https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/section_18\/9454f92bf736848a4de50bc5dadee26a.jpg\" \/>c.<img src=\"https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/section_18\/82512faf03c5d7f6d3bdacc4cc8b0946.jpg\" \/><\/div>\r\n<div>[\/hidden-answer]<\/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\">\n<div class=\"textbox learning-objectives\">\n<h3>Learning Objectives<\/h3>\n<div id=\"book-content\">\n<div id=\"gob-ch15_s10\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch15_s10_n01\" class=\"learning_objectives editable block\">\n<ol id=\"gob-ch15_s10_l01\" class=\"orderedlist\">\n<li>Describe phosphate esters.<\/li>\n<li>Understand why phosphate esters are important in living cells<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><span style=\"font-size: 1rem;text-align: initial\">Just as carboxylic acids do, inorganic acids such as nitric acid (HNO<\/span><sub class=\"subscript\" style=\"text-align: initial\">3<\/sub><span style=\"font-size: 1rem;text-align: initial\">), sulfuric acid (H<\/span><sub class=\"subscript\" style=\"text-align: initial\">2<\/sub><span style=\"font-size: 1rem;text-align: initial\">SO<\/span><sub class=\"subscript\" style=\"text-align: initial\">4<\/sub><span style=\"font-size: 1rem;text-align: initial\">), and phosphoric acid (H<\/span><sub class=\"subscript\" style=\"text-align: initial\">3<\/sub><span style=\"font-size: 1rem;text-align: initial\">PO<\/span><sub class=\"subscript\" style=\"text-align: initial\">4<\/sub><span style=\"font-size: 1rem;text-align: initial\">) also form esters. The esters of phosphoric acid are especially important in biochemistry. A phosphoric acid molecule can form a monoalkyl, a dialkyl, or a trialkyl ester by reaction with one, two, or three molecules of an alcohol.<\/span><\/p>\n<\/div>\n<\/div>\n<div id=\"book-content\">\n<div id=\"gob-ch15_s10\" class=\"section\" xml:lang=\"en\">\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\/21153422\/3cfccf769579de43236f74e8d70fb978.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch15_s10_p02\" class=\"para editable block\">Esters of pyrophosphoric acid and triphosphoric acid are also important in biochemistry.<\/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\/21153425\/decfc0a7b6e52e2b0572512036d0b010.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch15_s10_p03\" class=\"para editable block\">Esters of these acids are present in every plant and animal cell. They are biochemical intermediates in the transformation of food into usable energy. The bonds between phosphate units in adenosine triphosphate (ATP) are called <em class=\"emphasis\">phosphoanhydride<\/em> bonds. These are high-energy bonds that store energy from the metabolism of foods. Hydrolysis of ATP releases energy as it is needed for biochemical processes (for instance, for muscle contraction). Phosphate esters are also important structural constituents of phospholipids and nucleic acids. (For more information about phospholipids and nucleic acids, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-17\">Chapter 17 &#8220;Lipids&#8221;<\/a>, <a class=\"xref\" href=\"gob-ch17_s03#gob-ch17_s03\">Section 17.3 &#8220;Membranes and Membrane Lipids&#8221;<\/a>, and <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-19\">Chapter 19 &#8220;Nucleic Acids&#8221;<\/a>, respectively.)<\/p>\n<div id=\"gob-ch15_s10_n02\" class=\"callout block\">\n<div class=\"textbox\">\n<h3 class=\"title\">Note<\/h3>\n<p id=\"gob-ch15_s10_p04\" class=\"para\">The explosive nitroglycerin (glyceryl trinitrate) is an ester formed from glycerol and nitric acid. It is used in medicine to relieve chest pain in heart disease.<\/p>\n<\/div>\n<h3 class=\"title\"><img decoding=\"async\" class=\"aligncenter\" style=\"color: #373d3f;font-size: 1em;font-weight: normal\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21153428\/6de233d9e5a3bd8d5a3d6b048fe409bf.jpg\" alt=\"image\" \/><\/h3>\n<\/div>\n<div id=\"gob-ch15_s10_qs01\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch15_s10_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercise<\/h3>\n<ol id=\"gob-ch15_s10_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s10_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s10_qs01_p01\" class=\"para\">What compounds combine to form phosphate esters?<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<div id=\"gob-ch15_s10_qs01_ans\" class=\"qandaset block\">\n<div class=\"answer\">\n<p id=\"gob-ch15_s10_qs01_p02_ans\" class=\"para\">\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q577238\">Show Answer<\/span><\/p>\n<div id=\"q577238\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li class=\"para\">phosphoric acids and alcohols<\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s10_n04\" class=\"key_takeaways editable block\">\n<div class=\"textbox key-takeaways\">\n<h3 class=\"title\">Key Takeaways<\/h3>\n<ul id=\"gob-ch15_s10_l02\" class=\"itemizedlist\">\n<li>Inorganic acids such as H<sub class=\"subscript\">3<\/sub>PO<sub class=\"subscript\">4<\/sub> form esters.<\/li>\n<li>The esters of phosphoric acid are especially important in biochemistry.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div id=\"gob-ch15_s10_qs02_ans\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch15_s10_qs02\" class=\"qandaset block\">\n<h3 class=\"title\">Exercises<\/h3>\n<ol id=\"gob-ch15_s10_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch15_s10_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s10_qs02_p01\" class=\"para\">Draw the structure for each compound.<\/p>\n<ol id=\"gob-ch15_s10_qs02_l01\" class=\"orderedlist\">\n<li>diethyl hydrogen phosphate<\/li>\n<li>methyl dihydrogen phosphate<\/li>\n<li>1-glycerol phosphate<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch15_s10_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch15_s10_qs02_p02\" class=\"para\">Name each compound.<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<div class=\"informalfigure large\">a.\u00a0<img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21153431\/8f42e2480165047bc770f077a27e00de.jpg\" alt=\"image\" \/><\/div>\n<div class=\"informalfigure large\">b.\u00a0<img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21153434\/71fd1300e1e4879d02e74f50b320d5a7.jpg\" alt=\"image\" \/><\/div>\n<div class=\"informalfigure large\">c.\u00a0<img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21153437\/3571b9501086bf1a4543b7107aa23fc2.jpg\" alt=\"image\" \/><\/div>\n<div>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q434871\">Show Answer<\/span><\/p>\n<div id=\"q434871\" class=\"hidden-answer\" style=\"display: none\">1. a.<img decoding=\"async\" src=\"https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/section_18\/0f8343077d449118a179e7e52b18ec83.jpg\" alt=\"image\" \/>b.<img decoding=\"async\" src=\"https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/section_18\/9454f92bf736848a4de50bc5dadee26a.jpg\" alt=\"image\" \/>c.<img decoding=\"async\" src=\"https:\/\/saylordotorg.github.io\/text_the-basics-of-general-organic-and-biological-chemistry\/section_18\/82512faf03c5d7f6d3bdacc4cc8b0946.jpg\" alt=\"image\" \/><\/div>\n<div><\/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-1629\">\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":11,"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-1629","chapter","type-chapter","status-publish","hentry"],"part":1500,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1629","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":10,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1629\/revisions"}],"predecessor-version":[{"id":3550,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/1629\/revisions\/3550"}],"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\/1629\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/media?parent=1629"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=1629"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/contributor?post=1629"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/license?post=1629"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}