{"id":1388,"date":"2018-03-21T15:04:05","date_gmt":"2018-03-21T15:04:05","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/glycols-and-glycerol\/"},"modified":"2018-05-09T16:01:20","modified_gmt":"2018-05-09T16:01:20","slug":"glycols-and-glycerol","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/glycols-and-glycerol\/","title":{"raw":"14.6 Glycols and Glycerol","rendered":"14.6 Glycols and Glycerol"},"content":{"raw":"<div id=\"navbar-top\" class=\"navbar\"><\/div>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch14_s06\" class=\"section\" xml:lang=\"en\">\r\n<div id=\"gob-ch14_s06_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-ch14_s06_l01\" class=\"orderedlist\">\r\n \t<li>Describe the structure and uses of some common polyhydric alcohols.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<p id=\"gob-ch14_s06_p01\" class=\"para editable block\">Alcohols with two OH groups on adjacent carbon atoms are commonly known as <span class=\"margin_term\"><span class=\"glossterm\">glycols<\/span><\/span>. The most important of these is 1,2-ethanediol (the common name is ethylene glycol), a sweet, colorless, somewhat viscous liquid.<\/p>\r\n\r\n<div class=\"informalfigure large block\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150352\/191ae402a56372ad2c94e130982c7dce.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch14_s06_p02\" class=\"para editable block\">Another common glycol, 1,2-propanediol, is commonly called propylene glycol. Its physical properties are quite similar to those of ethylene glycol.<\/p>\r\n\r\n<div class=\"informalfigure large block\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150354\/d2bfd1ed1b8629878cdd7de425cc0df5.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch14_s06_p03\" class=\"para editable block\">Commonly called glycerol or glycerin, 1,2,3-propanetriol is the most important trihydroxy alcohol. Like the two glycols, it is a sweet, syrupy liquid. Glycerol is a product of the hydrolysis of fats and oils. (For more information about fats and oils, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-17\">Chapter 17 \"Lipids\"<\/a>, <a class=\"xref\" href=\"gob-ch17_s02#gob-ch17_s02\">Section 17.2 \"Fats and Oils\"<\/a>.)<\/p>\r\n\r\n<div class=\"informalfigure large block\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150357\/2a9238e470147f5687ee11e826b0e40f.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch14_s06_p04\" class=\"para editable block\">Ethylene glycol is the main ingredient in many antifreeze mixtures for automobile radiators. The two OH groups lead to extensive intermolecular hydrogen bonding. This results in a high boiling point\u2014198\u00b0C; thus ethylene glycol does not boil away when it is used as an antifreeze. It is also completely miscible with water. A solution of 60% ethylene glycol in water freezes at \u221249\u00b0C (\u221256\u00b0F) and thus protects an automobile radiator down to that temperature. Ethylene glycol is also used in the manufacture of polyester fiber and magnetic film used in tapes for recorders and computers.<\/p>\r\n\r\n<div id=\"gob-ch14_s06_n02\" class=\"callout block\">\r\n<div class=\"textbox shaded\">\r\n<div id=\"gob-ch14_s06_n02\" class=\"callout block\">\r\n<h3 class=\"title\">To Your Health: Glycols and Human Health<\/h3>\r\n<p id=\"gob-ch14_s06_p05\" class=\"para\">Ethylene glycol is quite toxic. Because it is sweet, pets often lap up spills of leaked antifreeze from a garage floor or driveway. Sometimes people, especially children, drink it. As with methanol, its toxicity is due to a metabolite. Liver enzymes oxidize ethylene glycol to oxalate ion.<\/p>\r\n\r\n<div class=\"informalfigure large\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150359\/996a4bdd7fc16d56527cb409d6dd1667.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch14_s06_p06\" class=\"para\">In the kidneys, the oxalate ion combines with the calcium (Ca<sup class=\"superscript\">2+<\/sup>) ion, precipitating as calcium oxalate (CaC<sub class=\"subscript\">2<\/sub>O<sub class=\"subscript\">4<\/sub>).<\/p>\r\n<span class=\"informalequation\"><span class=\"mathphrase\">Ca<sup class=\"superscript\">2+<\/sup>(aq) + C<sub class=\"subscript\">2<\/sub>O<sub class=\"subscript\">4<\/sub><sup class=\"superscript\">2\u2212<\/sup>(aq) \u2192 CaC<sub class=\"subscript\">2<\/sub>O<sub class=\"subscript\">4<\/sub>(s)<\/span><\/span>\r\n<p id=\"gob-ch14_s06_p07\" class=\"para\">These crystals cause renal damage and can lead to kidney failure and death.<\/p>\r\n<p id=\"gob-ch14_s06_p08\" class=\"para\">Although propylene glycol has physical properties much like those of ethylene glycol, its physiological properties are quite different. Propylene glycol is essentially nontoxic, and it can be used as a solvent for drugs and as a moisturizing agent for foods. Like other alcohols, propylene glycol is oxidized by liver enzymes.<\/p>\r\n\r\n<div class=\"informalfigure large\"><img src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150402\/ec12c1b219899ac46d6a703b367cea89.jpg\" alt=\"image\" \/><\/div>\r\n<p id=\"gob-ch14_s06_p09\" class=\"para\">In this case, however, the product is pyruvate ion, a normal intermediate in carbohydrate metabolism. (For more information about metabolic reactions, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-20\">Chapter 20 \"Energy Metabolism\"<\/a>.)<\/p>\r\n<p id=\"gob-ch14_s06_p10\" class=\"para\">Glycerol, a product of fat metabolism, is essentially nontoxic.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch14_s06_n02\" class=\"callout block\">\r\n<h3 class=\"title\">Concept Review Exercises<\/h3>\r\n<\/div>\r\n<div id=\"gob-ch14_s06_qs01\" class=\"qandaset block\">\r\n<ol id=\"gob-ch14_s06_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch14_s06_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s06_qs01_p01\" class=\"para\">In the oxidation of propylene glycol to pyruvic acid, what functional groups in the reactant are involved? What new functional groups appear in the product?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch14_s06_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s06_qs01_p03\" class=\"para\">Oxalate ion is formed by the oxidation of ethylene glycol. In what kind of reaction is the oxalate ion involved?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n[reveal-answer q=\"258766\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"258766\"]\r\n<ol>\r\n \t<li>two OH groups; a ketone group and a carboxylic acid group<\/li>\r\n \t<li>precipitation[\/hidden-answer]<\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch14_s06_qs01_ans\" class=\"qandaset block\">\r\n<div class=\"textbox key-takeaways\">\r\n<h3>Key Takeaways<\/h3>\r\n<div id=\"gob-ch14_s06_qs01_ans\" class=\"qandaset block\"><\/div>\r\n<div id=\"gob-ch14_s06_n04\" class=\"key_takeaways editable block\">\r\n<ul id=\"gob-ch14_s06_l03\" class=\"itemizedlist\">\r\n \t<li>Glycols are alcohols with two OH groups on adjacent carbon atoms.<\/li>\r\n \t<li>Glycerol is the most important trihydroxy alcohol.<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox exercises\">\r\n<h3>Exercises<\/h3>\r\n<div id=\"gob-ch14_s06_qs01_ans\" class=\"qandaset block\">\r\n\r\n&nbsp;\r\n\r\n<\/div>\r\n<div id=\"gob-ch14_s06_qs02\" class=\"qandaset block\">\r\n<ol id=\"gob-ch14_s06_qs02_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch14_s06_qs02_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s06_qs02_p01\" class=\"para\">What is a glycol?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch14_s06_qs02_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s06_qs02_p03\" class=\"para\">Why is ethylene glycol so much more toxic to humans than propylene glycol?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch14_s06_qs02_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s06_qs02_p05\" class=\"para\">Draw the structure for each compound.<\/p>\r\n\r\n<ol id=\"gob-ch14_s06_qs02_l01\" class=\"orderedlist\">\r\n \t<li>1,5-pentanediol<\/li>\r\n \t<li>propylene glycol<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch14_s06_qs02_qd01_qa04\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch14_s06_qs02_p06\" class=\"para\">Draw the structure for each compound.<\/p>\r\n\r\n<ol id=\"gob-ch14_s06_qs02_l03\" class=\"orderedlist\">\r\n \t<li>1,3-hexandiol<\/li>\r\n \t<li>glycerol<\/li>\r\n<\/ol>\r\n<\/div>\r\n&nbsp;<\/li>\r\n<\/ol>\r\n<span style=\"font-size: 1rem;text-align: initial\">[reveal-answer q=\"197424\"]Show Answer[\/reveal-answer]<\/span>\r\n\r\n[hidden-answer a=\"197424\"]\r\n\r\n1. an alcohol with two OH groups on adjacent carbon atoms\r\n\r\n3. a.\u00a0HOCH<sub class=\"subscript\">2<\/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>OH\r\n\r\nb.\u00a0<img style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150404\/30a7dc6a60ff0d8050b5faa558966f1c.jpg\" alt=\"image\" \/>[\/hidden-answer]\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-ch14_s06\" class=\"section\" xml:lang=\"en\">\n<div id=\"gob-ch14_s06_n01\" class=\"learning_objectives editable block\">\n<div class=\"textbox learning-objectives\">\n<h3 class=\"title\">Learning Objective<\/h3>\n<ol id=\"gob-ch14_s06_l01\" class=\"orderedlist\">\n<li>Describe the structure and uses of some common polyhydric alcohols.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<p id=\"gob-ch14_s06_p01\" class=\"para editable block\">Alcohols with two OH groups on adjacent carbon atoms are commonly known as <span class=\"margin_term\"><span class=\"glossterm\">glycols<\/span><\/span>. The most important of these is 1,2-ethanediol (the common name is ethylene glycol), a sweet, colorless, somewhat viscous liquid.<\/p>\n<div class=\"informalfigure large block\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150352\/191ae402a56372ad2c94e130982c7dce.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch14_s06_p02\" class=\"para editable block\">Another common glycol, 1,2-propanediol, is commonly called propylene glycol. Its physical properties are quite similar to those of ethylene glycol.<\/p>\n<div class=\"informalfigure large block\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150354\/d2bfd1ed1b8629878cdd7de425cc0df5.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch14_s06_p03\" class=\"para editable block\">Commonly called glycerol or glycerin, 1,2,3-propanetriol is the most important trihydroxy alcohol. Like the two glycols, it is a sweet, syrupy liquid. Glycerol is a product of the hydrolysis of fats and oils. (For more information about fats and oils, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-17\">Chapter 17 &#8220;Lipids&#8221;<\/a>, <a class=\"xref\" href=\"gob-ch17_s02#gob-ch17_s02\">Section 17.2 &#8220;Fats and Oils&#8221;<\/a>.)<\/p>\n<div class=\"informalfigure large block\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150357\/2a9238e470147f5687ee11e826b0e40f.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch14_s06_p04\" class=\"para editable block\">Ethylene glycol is the main ingredient in many antifreeze mixtures for automobile radiators. The two OH groups lead to extensive intermolecular hydrogen bonding. This results in a high boiling point\u2014198\u00b0C; thus ethylene glycol does not boil away when it is used as an antifreeze. It is also completely miscible with water. A solution of 60% ethylene glycol in water freezes at \u221249\u00b0C (\u221256\u00b0F) and thus protects an automobile radiator down to that temperature. Ethylene glycol is also used in the manufacture of polyester fiber and magnetic film used in tapes for recorders and computers.<\/p>\n<div id=\"gob-ch14_s06_n02\" class=\"callout block\">\n<div class=\"textbox shaded\">\n<div id=\"gob-ch14_s06_n02\" class=\"callout block\">\n<h3 class=\"title\">To Your Health: Glycols and Human Health<\/h3>\n<p id=\"gob-ch14_s06_p05\" class=\"para\">Ethylene glycol is quite toxic. Because it is sweet, pets often lap up spills of leaked antifreeze from a garage floor or driveway. Sometimes people, especially children, drink it. As with methanol, its toxicity is due to a metabolite. Liver enzymes oxidize ethylene glycol to oxalate ion.<\/p>\n<div class=\"informalfigure large\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150359\/996a4bdd7fc16d56527cb409d6dd1667.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch14_s06_p06\" class=\"para\">In the kidneys, the oxalate ion combines with the calcium (Ca<sup class=\"superscript\">2+<\/sup>) ion, precipitating as calcium oxalate (CaC<sub class=\"subscript\">2<\/sub>O<sub class=\"subscript\">4<\/sub>).<\/p>\n<p><span class=\"informalequation\"><span class=\"mathphrase\">Ca<sup class=\"superscript\">2+<\/sup>(aq) + C<sub class=\"subscript\">2<\/sub>O<sub class=\"subscript\">4<\/sub><sup class=\"superscript\">2\u2212<\/sup>(aq) \u2192 CaC<sub class=\"subscript\">2<\/sub>O<sub class=\"subscript\">4<\/sub>(s)<\/span><\/span><\/p>\n<p id=\"gob-ch14_s06_p07\" class=\"para\">These crystals cause renal damage and can lead to kidney failure and death.<\/p>\n<p id=\"gob-ch14_s06_p08\" class=\"para\">Although propylene glycol has physical properties much like those of ethylene glycol, its physiological properties are quite different. Propylene glycol is essentially nontoxic, and it can be used as a solvent for drugs and as a moisturizing agent for foods. Like other alcohols, propylene glycol is oxidized by liver enzymes.<\/p>\n<div class=\"informalfigure large\"><img decoding=\"async\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150402\/ec12c1b219899ac46d6a703b367cea89.jpg\" alt=\"image\" \/><\/div>\n<p id=\"gob-ch14_s06_p09\" class=\"para\">In this case, however, the product is pyruvate ion, a normal intermediate in carbohydrate metabolism. (For more information about metabolic reactions, see <a class=\"xref\" href=\"..\/suny-orgbiochemistry\/chapter\/introduction-20\">Chapter 20 &#8220;Energy Metabolism&#8221;<\/a>.)<\/p>\n<p id=\"gob-ch14_s06_p10\" class=\"para\">Glycerol, a product of fat metabolism, is essentially nontoxic.<\/p>\n<\/div>\n<\/div>\n<div class=\"textbox exercises\">\n<div id=\"gob-ch14_s06_n02\" class=\"callout block\">\n<h3 class=\"title\">Concept Review Exercises<\/h3>\n<\/div>\n<div id=\"gob-ch14_s06_qs01\" class=\"qandaset block\">\n<ol id=\"gob-ch14_s06_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch14_s06_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s06_qs01_p01\" class=\"para\">In the oxidation of propylene glycol to pyruvic acid, what functional groups in the reactant are involved? What new functional groups appear in the product?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch14_s06_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s06_qs01_p03\" class=\"para\">Oxalate ion is formed by the oxidation of ethylene glycol. In what kind of reaction is the oxalate ion involved?<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q258766\">Show Answer<\/span><\/p>\n<div id=\"q258766\" class=\"hidden-answer\" style=\"display: none\">\n<ol>\n<li>two OH groups; a ketone group and a carboxylic acid group<\/li>\n<li>precipitation<\/div>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch14_s06_qs01_ans\" class=\"qandaset block\">\n<div class=\"textbox key-takeaways\">\n<h3>Key Takeaways<\/h3>\n<div id=\"gob-ch14_s06_qs01_ans\" class=\"qandaset block\"><\/div>\n<div id=\"gob-ch14_s06_n04\" class=\"key_takeaways editable block\">\n<ul id=\"gob-ch14_s06_l03\" class=\"itemizedlist\">\n<li>Glycols are alcohols with two OH groups on adjacent carbon atoms.<\/li>\n<li>Glycerol is the most important trihydroxy alcohol.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<div class=\"textbox exercises\">\n<h3>Exercises<\/h3>\n<div id=\"gob-ch14_s06_qs01_ans\" class=\"qandaset block\">\n<p>&nbsp;<\/p>\n<\/div>\n<div id=\"gob-ch14_s06_qs02\" class=\"qandaset block\">\n<ol id=\"gob-ch14_s06_qs02_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch14_s06_qs02_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s06_qs02_p01\" class=\"para\">What is a glycol?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch14_s06_qs02_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s06_qs02_p03\" class=\"para\">Why is ethylene glycol so much more toxic to humans than propylene glycol?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch14_s06_qs02_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s06_qs02_p05\" class=\"para\">Draw the structure for each compound.<\/p>\n<ol id=\"gob-ch14_s06_qs02_l01\" class=\"orderedlist\">\n<li>1,5-pentanediol<\/li>\n<li>propylene glycol<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch14_s06_qs02_qd01_qa04\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch14_s06_qs02_p06\" class=\"para\">Draw the structure for each compound.<\/p>\n<ol id=\"gob-ch14_s06_qs02_l03\" class=\"orderedlist\">\n<li>1,3-hexandiol<\/li>\n<li>glycerol<\/li>\n<\/ol>\n<\/div>\n<p>&nbsp;<\/li>\n<\/ol>\n<p><span style=\"font-size: 1rem;text-align: initial\"><\/p>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q197424\">Show Answer<\/span><\/span><\/p>\n<div id=\"q197424\" class=\"hidden-answer\" style=\"display: none\">\n<p>1. an alcohol with two OH groups on adjacent carbon atoms<\/p>\n<p>3. a.\u00a0HOCH<sub class=\"subscript\">2<\/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>OH<\/p>\n<p>b.\u00a0<img decoding=\"async\" style=\"font-size: 0.9em\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21150404\/30a7dc6a60ff0d8050b5faa558966f1c.jpg\" alt=\"image\" \/><\/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-1388\">\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 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