{"id":2019,"date":"2018-03-21T16:18:33","date_gmt":"2018-03-21T16:18:33","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/peptides\/"},"modified":"2018-12-03T20:32:45","modified_gmt":"2018-12-03T20:32:45","slug":"peptides","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/peptides\/","title":{"raw":"18.3 Peptides","rendered":"18.3 Peptides"},"content":{"raw":"<div id=\"navbar-top\" class=\"navbar\"><\/div>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch18_s03\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch18_s03_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-ch18_s03_l01\" class=\"orderedlist\">\r\n \t<li>Explain how a peptide is formed from individual amino acids.<\/li>\r\n \t<li>Explain why the sequence of amino acids in a protein is important.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<p id=\"gob-ch18_s03_p01\" class=\"para editable block\">Two or more amino acids can join together into chains called peptides. In <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-15\">Chapter 15 \"Organic Acids and Bases and Some of Their Derivatives\"<\/a>, <a class=\"xref\" href=\"gob-ch15_s16#gob-ch15_s16\">Section 15.16 \"Formation of Amides\"<\/a>, we discussed the reaction between ammonia and a carboxylic acid to form an amide. In a similar reaction, the amino group on one amino acid molecule reacts with the carboxyl group on another, releasing a molecule of water and forming an amide linkage:<\/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\/21161818\/dc2b9c0a2720a543097192d3a1584b40.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch18_s03_p02\" class=\"para editable block\">An amide bond joining two amino acid units is called a <span class=\"margin_term\"><span class=\"glossterm\">peptide bond<\/span><\/span>. Note that the product molecule still has a reactive amino group on the left and a reactive carboxyl group on the right. These can react with additional amino acids to lengthen the peptide. The process can continue until thousands of units have joined, resulting in large proteins.<\/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\/21161821\/845e1892447f21d1b0abbece7930f344.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch18_s03_p03\" class=\"para editable block\">A chain consisting of only two amino acid units is called a <em class=\"emphasis\">dipeptide<\/em>; a chain consisting of three is a <em class=\"emphasis\">tripeptide<\/em>. By convention, peptide and protein structures are depicted with the amino acid whose amino group is free (the N-terminal end) on the left and the amino acid with a free carboxyl group (the C-terminal end) to the right.<\/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\/21161826\/e8fee7b1e9c1c1cff3447816e529e10f.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch18_s03_p04\" class=\"para editable block\">The general term <em class=\"emphasis\">peptide<\/em> refers to an amino acid chain of unspecified length. However, chains of about 50 amino acids or more are usually called proteins or <span class=\"margin_term\"><span class=\"glossterm\">polypeptides<\/span><\/span>. In its physiologically active form, a protein may be composed of one or more polypeptide chains.<\/p>\r\n<p id=\"gob-ch18_s03_p05\" class=\"para editable block\">For peptides and proteins to be physiologically active, it is not enough that they incorporate certain amounts of specific amino acids. The order, or <em class=\"emphasis\">sequence<\/em>, in which the amino acids are connected is also of critical importance. Bradykinin is a nine-amino acid peptide produced in the blood that has the following amino acid sequence:<\/p>\r\n<span class=\"informalequation block\"><span class=\"mathphrase\">arg-pro-pro-gly-phe-ser-pro-phe-arg<\/span><\/span>\r\n<p id=\"gob-ch18_s03_p06\" class=\"para editable block\">This peptide lowers blood pressure, stimulates smooth muscle tissue, increases capillary permeability, and causes pain. When the order of amino acids in bradykinin is reversed,<\/p>\r\n<span class=\"informalequation block\"><span class=\"mathphrase\">arg-phe-pro-ser-phe-gly-pro-pro-arg<\/span><\/span>\r\n<p id=\"gob-ch18_s03_p07\" class=\"para editable block\">the peptide resulting from this synthesis shows none of the activity of bradykinin.<\/p>\r\n<p id=\"gob-ch18_s03_p08\" class=\"para editable block\">Just as millions of different words are spelled with our 26-letter English alphabet, millions of different proteins are made with the 20 common amino acids. However, just as the English alphabet can be used to write gibberish, amino acids can be put together in the <em class=\"emphasis\">wrong sequence<\/em> to produce nonfunctional proteins. Although the correct sequence is ordinarily of utmost importance, it is not always absolutely required. Just as you can sometimes make sense of incorrectly spelled English words, a protein with a small percentage of \u201cincorrect\u201d amino acids may continue to function. However, it rarely functions as well as a protein having the correct sequence. There are also instances in which seemingly minor errors of sequence have disastrous effects. For example, in some people, every molecule of hemoglobin (a protein in the blood that transports oxygen) has a single incorrect amino acid unit out of about 300 (a single valine replaces a glutamic acid). That \u201cminor\u201d error is responsible for sickle cell anemia, an inherited condition that negatively\u00a0 impacts quality and quantity of life.<\/p>\r\n\r\n<div id=\"gob-ch18_s03_qs01\" class=\"qandaset block\">\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch18_s03_qs01\" class=\"qandaset block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<ol id=\"gob-ch18_s03_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch18_s03_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch18_s03_qs01_p01\" class=\"para\">Distinguish between the N-terminal amino acid and the C-terminal amino acid of a peptide or protein.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch18_s03_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch18_s03_qs01_p03\" class=\"para\">Describe the difference between an amino acid and a peptide.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch18_s03_qs01_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch18_s03_qs01_p05\" class=\"para\">Amino acid units in a protein are connected by peptide bonds. What is another name for the functional group linking the amino acids?<\/p>\r\n\r\n<\/div>\r\n&nbsp;<\/li>\r\n<\/ol>\r\n[reveal-answer q=\"564432\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"564432\"]\r\n<ol>\r\n \t<li>The N-terminal end is the end of a peptide or protein whose amino group is free (not involved in the formation of a peptide bond), while the C-terminal end has a free carboxyl group.<\/li>\r\n \t<li>A peptide is composed of two or more amino acids. Amino acids are the building blocks of peptides.<\/li>\r\n \t<li>amide bond[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch18_s03_n03\" class=\"key_takeaways editable block\">\r\n<div class=\"textbox key-takeaways\">\r\n<div id=\"gob-ch18_s03_n03\" class=\"key_takeaways editable block\">\r\n<h3 class=\"title\">Key Takeaways<\/h3>\r\n<ul id=\"gob-ch18_s03_l03\" class=\"itemizedlist\">\r\n \t<li>The amino group of one amino acid can react with the carboxyl group on another amino acid to form a peptide bond that links the two amino acids together. Additional amino acids can be added on through the formation of addition peptide (amide) bonds.<\/li>\r\n \t<li>A sequence of amino acids in a peptide or protein is written with the N-terminal amino acid first and the C-terminal amino acid at the end (writing left to right).<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch18_s03_n03\" class=\"key_takeaways editable block\">\r\n<h3 class=\"title\">Exercises<\/h3>\r\n<\/div>\r\n<div id=\"gob-ch18_s03_qs02\" class=\"qandaset block\">\r\n<ol id=\"gob-ch18_s03_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch18_s03_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch18_s03_qs02_p01\" class=\"para\">Draw the structure for each peptide.<\/p>\r\n\r\n<ol id=\"gob-ch18_s03_qs02_l01\" class=\"orderedlist\">\r\n \t<li>gly-val<\/li>\r\n \t<li>val-gly<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch18_s03_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch18_s03_qs02_p02\" class=\"para\">Draw the structure for cys-val-ala.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch18_s03_qs02_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch18_s03_qs02_p03\" class=\"para\">Identify the C- and N-terminal amino acids for the peptide lys-val-phe-gly-arg-cys.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch18_s03_qs02_qd01_qa04\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch18_s03_qs02_p05\" class=\"para\">Identify the C- and N-terminal amino acids for the peptide asp-arg-val-tyr-ile-his-pro-phe.<\/p>\r\n\r\n<\/div>\r\n&nbsp;<\/li>\r\n<\/ol>\r\n[reveal-answer q=\"501027\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"501027\"]\r\n\r\n1. a.\u00a0<img class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21161829\/11673f1d38b19a90480d2e4f44636525.jpg\" alt=\"image\" \/>\r\n\r\n<span style=\"font-size: 1rem;text-align: initial\">b.\u00a0<\/span><img class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21161831\/8e5098390ccb1ec2ad6ae60f20028300.jpg\" alt=\"image\" \/>\r\n\r\n<span style=\"font-size: 1rem;text-align: initial\">c.\u00a0C-terminal amino acid: cys; N-terminal amino acid: lys [\/hidden-answer]<\/span>\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<\/div>","rendered":"<div id=\"navbar-top\" class=\"navbar\"><\/div>\n<div id=\"book-content\">\n<div id=\"gob-ch18_s03\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch18_s03_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<h3 class=\"title\">Learning Objectives<\/h3>\n<ol id=\"gob-ch18_s03_l01\" class=\"orderedlist\">\n<li>Explain how a peptide is formed from individual amino acids.<\/li>\n<li>Explain why the sequence of amino acids in a protein is important.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<p id=\"gob-ch18_s03_p01\" class=\"para editable block\">Two or more amino acids can join together into chains called peptides. In <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-15\">Chapter 15 &#8220;Organic Acids and Bases and Some of Their Derivatives&#8221;<\/a>, <a class=\"xref\" href=\"gob-ch15_s16#gob-ch15_s16\">Section 15.16 &#8220;Formation of Amides&#8221;<\/a>, we discussed the reaction between ammonia and a carboxylic acid to form an amide. In a similar reaction, the amino group on one amino acid molecule reacts with the carboxyl group on another, releasing a molecule of water and forming an amide linkage:<\/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\/21161818\/dc2b9c0a2720a543097192d3a1584b40.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch18_s03_p02\" class=\"para editable block\">An amide bond joining two amino acid units is called a <span class=\"margin_term\"><span class=\"glossterm\">peptide bond<\/span><\/span>. Note that the product molecule still has a reactive amino group on the left and a reactive carboxyl group on the right. These can react with additional amino acids to lengthen the peptide. The process can continue until thousands of units have joined, resulting in large proteins.<\/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\/21161821\/845e1892447f21d1b0abbece7930f344.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch18_s03_p03\" class=\"para editable block\">A chain consisting of only two amino acid units is called a <em class=\"emphasis\">dipeptide<\/em>; a chain consisting of three is a <em class=\"emphasis\">tripeptide<\/em>. By convention, peptide and protein structures are depicted with the amino acid whose amino group is free (the N-terminal end) on the left and the amino acid with a free carboxyl group (the C-terminal end) to the right.<\/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\/21161826\/e8fee7b1e9c1c1cff3447816e529e10f.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch18_s03_p04\" class=\"para editable block\">The general term <em class=\"emphasis\">peptide<\/em> refers to an amino acid chain of unspecified length. However, chains of about 50 amino acids or more are usually called proteins or <span class=\"margin_term\"><span class=\"glossterm\">polypeptides<\/span><\/span>. In its physiologically active form, a protein may be composed of one or more polypeptide chains.<\/p>\n<p id=\"gob-ch18_s03_p05\" class=\"para editable block\">For peptides and proteins to be physiologically active, it is not enough that they incorporate certain amounts of specific amino acids. The order, or <em class=\"emphasis\">sequence<\/em>, in which the amino acids are connected is also of critical importance. Bradykinin is a nine-amino acid peptide produced in the blood that has the following amino acid sequence:<\/p>\n<p><span class=\"informalequation block\"><span class=\"mathphrase\">arg-pro-pro-gly-phe-ser-pro-phe-arg<\/span><\/span><\/p>\n<p id=\"gob-ch18_s03_p06\" class=\"para editable block\">This peptide lowers blood pressure, stimulates smooth muscle tissue, increases capillary permeability, and causes pain. When the order of amino acids in bradykinin is reversed,<\/p>\n<p><span class=\"informalequation block\"><span class=\"mathphrase\">arg-phe-pro-ser-phe-gly-pro-pro-arg<\/span><\/span><\/p>\n<p id=\"gob-ch18_s03_p07\" class=\"para editable block\">the peptide resulting from this synthesis shows none of the activity of bradykinin.<\/p>\n<p id=\"gob-ch18_s03_p08\" class=\"para editable block\">Just as millions of different words are spelled with our 26-letter English alphabet, millions of different proteins are made with the 20 common amino acids. However, just as the English alphabet can be used to write gibberish, amino acids can be put together in the <em class=\"emphasis\">wrong sequence<\/em> to produce nonfunctional proteins. Although the correct sequence is ordinarily of utmost importance, it is not always absolutely required. Just as you can sometimes make sense of incorrectly spelled English words, a protein with a small percentage of \u201cincorrect\u201d amino acids may continue to function. However, it rarely functions as well as a protein having the correct sequence. There are also instances in which seemingly minor errors of sequence have disastrous effects. For example, in some people, every molecule of hemoglobin (a protein in the blood that transports oxygen) has a single incorrect amino acid unit out of about 300 (a single valine replaces a glutamic acid). That \u201cminor\u201d error is responsible for sickle cell anemia, an inherited condition that negatively\u00a0 impacts quality and quantity of life.<\/p>\n<div id=\"gob-ch18_s03_qs01\" class=\"qandaset block\">\n<div class=\"textbox exercises\">\n<div id=\"gob-ch18_s03_qs01\" class=\"qandaset block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<ol id=\"gob-ch18_s03_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch18_s03_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch18_s03_qs01_p01\" class=\"para\">Distinguish between the N-terminal amino acid and the C-terminal amino acid of a peptide or protein.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch18_s03_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch18_s03_qs01_p03\" class=\"para\">Describe the difference between an amino acid and a peptide.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch18_s03_qs01_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch18_s03_qs01_p05\" class=\"para\">Amino acid units in a protein are connected by peptide bonds. What is another name for the functional group linking the amino acids?<\/p>\n<\/div>\n<p>&nbsp;<\/li>\n<\/ol>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q564432\">Show Answer<\/span><\/p>\n<div id=\"q564432\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li>The N-terminal end is the end of a peptide or protein whose amino group is free (not involved in the formation of a peptide bond), while the C-terminal end has a free carboxyl group.<\/li>\n<li>A peptide is composed of two or more amino acids. Amino acids are the building blocks of peptides.<\/li>\n<li>amide bond<\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch18_s03_n03\" class=\"key_takeaways editable block\">\n<div class=\"textbox key-takeaways\">\n<div id=\"gob-ch18_s03_n03\" class=\"key_takeaways editable block\">\n<h3 class=\"title\">Key Takeaways<\/h3>\n<ul id=\"gob-ch18_s03_l03\" class=\"itemizedlist\">\n<li>The amino group of one amino acid can react with the carboxyl group on another amino acid to form a peptide bond that links the two amino acids together. Additional amino acids can be added on through the formation of addition peptide (amide) bonds.<\/li>\n<li>A sequence of amino acids in a peptide or protein is written with the N-terminal amino acid first and the C-terminal amino acid at the end (writing left to right).<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div class=\"textbox exercises\">\n<div id=\"gob-ch18_s03_n03\" class=\"key_takeaways editable block\">\n<h3 class=\"title\">Exercises<\/h3>\n<\/div>\n<div id=\"gob-ch18_s03_qs02\" class=\"qandaset block\">\n<ol id=\"gob-ch18_s03_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch18_s03_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch18_s03_qs02_p01\" class=\"para\">Draw the structure for each peptide.<\/p>\n<ol id=\"gob-ch18_s03_qs02_l01\" class=\"orderedlist\">\n<li>gly-val<\/li>\n<li>val-gly<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch18_s03_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch18_s03_qs02_p02\" class=\"para\">Draw the structure for cys-val-ala.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch18_s03_qs02_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch18_s03_qs02_p03\" class=\"para\">Identify the C- and N-terminal amino acids for the peptide lys-val-phe-gly-arg-cys.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch18_s03_qs02_qd01_qa04\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch18_s03_qs02_p05\" class=\"para\">Identify the C- and N-terminal amino acids for the peptide asp-arg-val-tyr-ile-his-pro-phe.<\/p>\n<\/div>\n<p>&nbsp;<\/li>\n<\/ol>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q501027\">Show Answer<\/span><\/p>\n<div id=\"q501027\" class=\"hidden-answer\" style=\"display: none\">\n<p>1. a.\u00a0<img decoding=\"async\" class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21161829\/11673f1d38b19a90480d2e4f44636525.jpg\" alt=\"image\" \/><\/p>\n<p><span style=\"font-size: 1rem;text-align: initial\">b.\u00a0<\/span><img decoding=\"async\" class=\"aligncenter\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21161831\/8e5098390ccb1ec2ad6ae60f20028300.jpg\" alt=\"image\" \/><\/p>\n<p><span style=\"font-size: 1rem;text-align: initial\">c.\u00a0C-terminal amino acid: cys; N-terminal amino acid: lys <\/div>\n<\/div>\n<p><\/span><\/p>\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-2019\">\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":4,"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-2019","chapter","type-chapter","status-publish","hentry"],"part":1956,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/2019","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":9,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/2019\/revisions"}],"predecessor-version":[{"id":3620,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/2019\/revisions\/3620"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/parts\/1956"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapters\/2019\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/media?parent=2019"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/pressbooks\/v2\/chapter-type?post=2019"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/contributor?post=2019"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/wp-json\/wp\/v2\/license?post=2019"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}