{"id":1948,"date":"2018-03-21T16:11:33","date_gmt":"2018-03-21T16:11:33","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-orgbiochemistry\/chapter\/end-of-chapter-material-8\/"},"modified":"2018-11-26T21:28:30","modified_gmt":"2018-11-26T21:28:30","slug":"end-of-chapter-material-8","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-monroecc-orgbiochemistry\/chapter\/end-of-chapter-material-8\/","title":{"raw":"17.5 End-of-Chapter Material","rendered":"17.5 End-of-Chapter Material"},"content":{"raw":"<div id=\"navbar-top\" class=\"navbar\"><\/div>\r\n<div id=\"book-content\">\r\n<div id=\"gob-ch17_s05\" class=\"section end-of-chapter\" xml:lang=\"en\">\r\n<div id=\"gob-ch17_s05_n01\" class=\"callout editable block\">\r\n<div class=\"textbox shaded\">\r\n<div id=\"gob-ch17_s05_n01\" class=\"callout editable block\">\r\n<h3 class=\"title\">Chapter Summary<\/h3>\r\n<p id=\"gob-ch17_s05_p01\" class=\"para\"><em class=\"emphasis\">To ensure that you understand the material in this chapter, you should review the meanings of the bold terms in the following summary and ask yourself how they relate to the topics in the chapter.<\/em><\/p>\r\n<p id=\"gob-ch17_s05_p02\" class=\"para\"><strong class=\"emphasis bold\">Lipids<\/strong>, found in the body tissues of all organisms, are compounds that are more soluble in organic solvents than in water. Many of them contain <strong class=\"emphasis bold\">fatty acids<\/strong>, which are carboxylic acids that generally contain an even number of 4\u201320 carbon atoms in an unbranched chain. <strong class=\"emphasis bold\">Saturated fatty acids<\/strong> have no carbon-to-carbon double bonds. <strong class=\"emphasis bold\">Monounsaturated fatty acids<\/strong> have a single carbon-to-carbon double bond, while <strong class=\"emphasis bold\">polyunsaturated fatty acids<\/strong> have more than one carbon-to-carbon double bond. Linoleic and linolenic acid are known as <strong class=\"emphasis bold\">essential fatty acids<\/strong> because the human body cannot synthesize these polyunsaturated fatty acids. The lipids known as <strong class=\"emphasis bold\">fats<\/strong> and <strong class=\"emphasis bold\">oils<\/strong> are triacylglycerols, more commonly called <strong class=\"emphasis bold\">triglycerides<\/strong>\u2014esters composed of three fatty acids joined to the trihydroxy alcohol glycerol. Fats are triglycerides that are solid at room temperature, and oils are triglycerides that are liquid at room temperature. Fats are found mainly in animals, and oils found mainly in plants. <em class=\"emphasis\">Saturated triglycerides<\/em> are those containing a higher proportion of saturated fatty acid chains (fewer carbon-to-carbon double bonds); <em class=\"emphasis\">unsaturated triglycerides<\/em> contain a higher proportion of unsaturated fatty acid chains.<\/p>\r\n<p id=\"gob-ch17_s05_p03\" class=\"para\"><strong class=\"emphasis bold\">Saponification<\/strong> is the hydrolysis of a triglyceride in a basic solution to form glycerol and three carboxylate anions or soap molecules. Other important reactions are the hydrogenation and oxidation of double bonds in unsaturated fats and oils.<\/p>\r\n<p id=\"gob-ch17_s05_p04\" class=\"para\"><strong class=\"emphasis bold\">Phospholipids<\/strong> are lipids containing phosphorus. In <strong class=\"emphasis bold\">phosphoglycerides<\/strong>, the phosphorus is joined to an amino alcohol unit. Some phosphoglycerides, like lecithins, are used to stabilize an <strong class=\"emphasis bold\">emulsion<\/strong>\u2014a dispersion of two liquids that do not normally mix, such as oil and water. <strong class=\"emphasis bold\">Sphingolipids<\/strong> are lipids for which the precursor is the amino alcohol sphingosine, rather than glycerol. A <strong class=\"emphasis bold\">glycolipid<\/strong> has a sugar substituted at one of the OH groups of either glycerol or sphingosine. All are highly polar lipids found in cell membranes.<\/p>\r\n<p id=\"gob-ch17_s05_p05\" class=\"para\">Polar lipids have dual characteristics: one part of the molecule is ionic and dissolves in water; the rest has a hydrocarbon structure and dissolves in nonpolar substances. Often, the ionic part is referred to as <strong class=\"emphasis bold\">hydrophilic<\/strong> (literally, \u201cwater loving\u201d) and the nonpolar part as <strong class=\"emphasis bold\">hydrophobic<\/strong> (\u201cwater fearing\u201d). When placed in water, polar lipids disperse into any one of three arrangements: <em class=\"emphasis\">micelles<\/em>, <em class=\"emphasis\">monolayers<\/em>, and <em class=\"emphasis\">bilayers<\/em>. <strong class=\"emphasis bold\">Micelles<\/strong> are aggregations of molecules in which the hydrocarbon tails of the lipids, being hydrophobic, are directed inward (away from the surrounding water), and the hydrophilic heads that are directed outward into the water. <strong class=\"emphasis bold\">Bilayers<\/strong> are double layers arranged so that the hydrophobic tails are sandwiched between the two layers of hydrophilic heads, which remain in contact with the water.<\/p>\r\n<p id=\"gob-ch17_s05_p06\" class=\"para\">Every living cell is enclosed by a <em class=\"emphasis\">cell membrane<\/em> composed of a lipid bilayer. In animal cells, the bilayer consists mainly of phospholipids, glycolipids, and the steroid cholesterol. Embedded in the bilayer are <strong class=\"emphasis bold\">integral proteins<\/strong>, and <strong class=\"emphasis bold\">peripheral proteins<\/strong> are loosely associated with the surface of the bilayer. Everything between the cell membrane and the membrane of the cell nucleus is called the <strong class=\"emphasis bold\">cytoplasm<\/strong>.<\/p>\r\n<p id=\"gob-ch17_s05_p07\" class=\"para\">Most lipids can be saponified, but some, such as <strong class=\"emphasis bold\">steroids<\/strong>, cannot be saponified. The steroid <strong class=\"emphasis bold\">cholesterol<\/strong> is found in animal cells but not in appreciable quantities in plant cells. It is a main component of all animal cell membranes and a precursor for hormones, vitamin D, and bile salts. Bile salts are the most important constituents of <strong class=\"emphasis bold\">bile<\/strong>, which is a yellowish-green liquid secreted by the gallbladder into the small intestine and is needed for the proper digestion of lipids.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<div class=\"textbox exercises\">\r\n<div id=\"gob-ch17_s05_n01\" class=\"callout editable block\">\r\n<h3 class=\"title\">Additional Exercises<\/h3>\r\n<\/div>\r\n<div id=\"gob-ch17_s05_qs01\" class=\"qandaset block\">\r\n<ol id=\"gob-ch17_s05_qs01_qd01\" class=\"qandadiv\">\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa01\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p01\" class=\"para\">The melting point of elaidic acid is 52\u00b0C.<\/p>\r\n\r\n<ol id=\"gob-ch17_s05_qs01_l01\" class=\"orderedlist\">\r\n \t<li>What trend is observed when comparing the melting points of elaidic acid, oleic acid, and stearic acid? Explain.<\/li>\r\n \t<li>\r\n<p class=\"para\">Would you expect the melting point of palmitelaidic acid to be lower or higher than that of elaidic acid? Explain.<\/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\/21161109\/0270c4c45ab6484444b6fed4ac626491.jpg\" alt=\"image\" \/><\/div><\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa02\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p02\" class=\"para\">Examine the labels on two brands of margarine and two brands of shortening and list the oils used in the various brands.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa03\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p04\" class=\"para\">Draw a typical lecithin molecule that incorporates glycerol, palmitic acid, oleic acid, phosphoric acid, and choline. Circle all the ester bonds.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa04\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p05\" class=\"para\">In cerebrosides, is the linkage between the fatty acid and sphingosine an amide bond or an ester bond? Justify your answer.<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa05\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p07\" class=\"para\">Serine is an amino acid that has the following structure. Draw the structure for a phosphatidylserine that contains a palmitic acid and a palmitoleic acid unit.<\/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\/21161113\/d6337e89bff3a69089a0fe5e9eb01a8a.jpg\" alt=\"image\" \/><\/div>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa06\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p08\" class=\"para\">Explain whether each compound would be expected to diffuse through the lipid bilayer of a cell membrane.<\/p>\r\n\r\n<ol id=\"gob-ch17_s05_qs01_l03\" class=\"orderedlist\">\r\n \t<li>potassium chloride<\/li>\r\n \t<li>CH<sub class=\"subscript\">3<\/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>CH<sub class=\"subscript\">3<\/sub><\/li>\r\n \t<li>fructose<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa07\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p09\" class=\"para\">Identify the role of each steroid hormone in the body.<\/p>\r\n\r\n<ol id=\"gob-ch17_s05_qs01_l05\" class=\"orderedlist\">\r\n \t<li>progesterone<\/li>\r\n \t<li>aldosterone<\/li>\r\n \t<li>testosterone<\/li>\r\n \t<li>cortisol<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa08\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p10\" class=\"para\">How does the structure of cholic acid differ from that of cholesterol? Which compound would you expect to be more polar? Why?<\/p>\r\n\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa09\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<ol id=\"gob-ch17_s05_qs01_l07\" class=\"orderedlist\">\r\n \t<li>What fatty acid is the precursor for the prostaglandins?<\/li>\r\n \t<li>Identify three biological effects of prostaglandins.<\/li>\r\n<\/ol>\r\n<\/div><\/li>\r\n \t<li id=\"gob-ch17_s05_qs01_qd01_qa10\" class=\"qandaentry\">\r\n<div class=\"question\">\r\n<p id=\"gob-ch17_s05_qs01_p13\" class=\"para\">Why is it important to determine the ratio of LDLs to HDLs, rather than just the concentration of serum cholesterol?<\/p>\r\n\r\n<\/div><\/li>\r\n<\/ol>\r\n<\/div>\r\n<\/div>\r\n<\/div>\r\n<div id=\"gob-ch17_s05_qs01_ans\" class=\"qandaset block\">\r\n<div class=\"answer\">\r\n<div class=\"textbox exercises\">\r\n<h3>Answers<\/h3>\r\n[reveal-answer q=\"268154\"]Show Answer[\/reveal-answer]\r\n[hidden-answer a=\"268154\"]\r\n\r\n1. a. Stearic acid has the highest melting point, followed by elaidic acid, and then oleic acid with the lowest melting point. Elaidic acid is a <em class=\"emphasis\">trans<\/em> fatty acid, and the carbon chains can pack together almost as tightly as those of the saturated stearic acid. Oleic acid is a <em class=\"emphasis\">cis<\/em> fatty acid, and the bend in the hydrocarbon chain keeps these carbon chains from packing as closely together; fewer interactions lead to a much lower melting point.\r\n\r\nb. The melting point of palmitelaidic acid should be lower than that of elaidic acid because it has a shorter carbon chain (16, as compared to 18 for elaidic acid). The shorter the carbon chain, the lower the melting point due to a decrease in intermolecular interactions, assuming other factors such as the number of carbon-to-carbon double bonds is the same.\r\n<div class=\"answer\"><\/div>\r\n<div class=\"answer\">\r\n<div class=\"informalfigure large\">3.<img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21161123\/2f72b31967541a6516059225e6511ef1.jpg\" alt=\"image\" \/><\/div>\r\n<\/div>\r\n<div class=\"answer\"><\/div>\r\n<div class=\"answer\">\r\n<div class=\"informalfigure large\">5.\u00a0<img class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21161130\/39f11c5526ff31b33f7a95b80db827e1.jpg\" alt=\"image\" \/><\/div>\r\n<\/div>\r\n<div class=\"answer\"><\/div>\r\n<div class=\"answer\">\r\n\r\n7. a. regulates the menstrual cycle and maintains pregnancy\r\n\r\nb. regulates salt metabolism by stimulating the kidneys to retain sodium and excrete potassium\r\n\r\nc. stimulates and maintains male sex characteristics\r\n\r\nd. stimulates the conversion of proteins to carbohydrates\r\n\r\n<\/div>\r\n<div class=\"answer\"><\/div>\r\n<div class=\"answer\">\r\n\r\n9. a. arachidonic acid\r\n\r\nb. induce smooth muscle contraction, lower blood pressure, and contribute to the inflammatory response\u00a0[\/hidden-answer]\r\n\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\"><\/div>\n<div id=\"book-content\">\n<div id=\"gob-ch17_s05\" class=\"section end-of-chapter\" xml:lang=\"en\">\n<div id=\"gob-ch17_s05_n01\" class=\"callout editable block\">\n<div class=\"textbox shaded\">\n<div id=\"gob-ch17_s05_n01\" class=\"callout editable block\">\n<h3 class=\"title\">Chapter Summary<\/h3>\n<p id=\"gob-ch17_s05_p01\" class=\"para\"><em class=\"emphasis\">To ensure that you understand the material in this chapter, you should review the meanings of the bold terms in the following summary and ask yourself how they relate to the topics in the chapter.<\/em><\/p>\n<p id=\"gob-ch17_s05_p02\" class=\"para\"><strong class=\"emphasis bold\">Lipids<\/strong>, found in the body tissues of all organisms, are compounds that are more soluble in organic solvents than in water. Many of them contain <strong class=\"emphasis bold\">fatty acids<\/strong>, which are carboxylic acids that generally contain an even number of 4\u201320 carbon atoms in an unbranched chain. <strong class=\"emphasis bold\">Saturated fatty acids<\/strong> have no carbon-to-carbon double bonds. <strong class=\"emphasis bold\">Monounsaturated fatty acids<\/strong> have a single carbon-to-carbon double bond, while <strong class=\"emphasis bold\">polyunsaturated fatty acids<\/strong> have more than one carbon-to-carbon double bond. Linoleic and linolenic acid are known as <strong class=\"emphasis bold\">essential fatty acids<\/strong> because the human body cannot synthesize these polyunsaturated fatty acids. The lipids known as <strong class=\"emphasis bold\">fats<\/strong> and <strong class=\"emphasis bold\">oils<\/strong> are triacylglycerols, more commonly called <strong class=\"emphasis bold\">triglycerides<\/strong>\u2014esters composed of three fatty acids joined to the trihydroxy alcohol glycerol. Fats are triglycerides that are solid at room temperature, and oils are triglycerides that are liquid at room temperature. Fats are found mainly in animals, and oils found mainly in plants. <em class=\"emphasis\">Saturated triglycerides<\/em> are those containing a higher proportion of saturated fatty acid chains (fewer carbon-to-carbon double bonds); <em class=\"emphasis\">unsaturated triglycerides<\/em> contain a higher proportion of unsaturated fatty acid chains.<\/p>\n<p id=\"gob-ch17_s05_p03\" class=\"para\"><strong class=\"emphasis bold\">Saponification<\/strong> is the hydrolysis of a triglyceride in a basic solution to form glycerol and three carboxylate anions or soap molecules. Other important reactions are the hydrogenation and oxidation of double bonds in unsaturated fats and oils.<\/p>\n<p id=\"gob-ch17_s05_p04\" class=\"para\"><strong class=\"emphasis bold\">Phospholipids<\/strong> are lipids containing phosphorus. In <strong class=\"emphasis bold\">phosphoglycerides<\/strong>, the phosphorus is joined to an amino alcohol unit. Some phosphoglycerides, like lecithins, are used to stabilize an <strong class=\"emphasis bold\">emulsion<\/strong>\u2014a dispersion of two liquids that do not normally mix, such as oil and water. <strong class=\"emphasis bold\">Sphingolipids<\/strong> are lipids for which the precursor is the amino alcohol sphingosine, rather than glycerol. A <strong class=\"emphasis bold\">glycolipid<\/strong> has a sugar substituted at one of the OH groups of either glycerol or sphingosine. All are highly polar lipids found in cell membranes.<\/p>\n<p id=\"gob-ch17_s05_p05\" class=\"para\">Polar lipids have dual characteristics: one part of the molecule is ionic and dissolves in water; the rest has a hydrocarbon structure and dissolves in nonpolar substances. Often, the ionic part is referred to as <strong class=\"emphasis bold\">hydrophilic<\/strong> (literally, \u201cwater loving\u201d) and the nonpolar part as <strong class=\"emphasis bold\">hydrophobic<\/strong> (\u201cwater fearing\u201d). When placed in water, polar lipids disperse into any one of three arrangements: <em class=\"emphasis\">micelles<\/em>, <em class=\"emphasis\">monolayers<\/em>, and <em class=\"emphasis\">bilayers<\/em>. <strong class=\"emphasis bold\">Micelles<\/strong> are aggregations of molecules in which the hydrocarbon tails of the lipids, being hydrophobic, are directed inward (away from the surrounding water), and the hydrophilic heads that are directed outward into the water. <strong class=\"emphasis bold\">Bilayers<\/strong> are double layers arranged so that the hydrophobic tails are sandwiched between the two layers of hydrophilic heads, which remain in contact with the water.<\/p>\n<p id=\"gob-ch17_s05_p06\" class=\"para\">Every living cell is enclosed by a <em class=\"emphasis\">cell membrane<\/em> composed of a lipid bilayer. In animal cells, the bilayer consists mainly of phospholipids, glycolipids, and the steroid cholesterol. Embedded in the bilayer are <strong class=\"emphasis bold\">integral proteins<\/strong>, and <strong class=\"emphasis bold\">peripheral proteins<\/strong> are loosely associated with the surface of the bilayer. Everything between the cell membrane and the membrane of the cell nucleus is called the <strong class=\"emphasis bold\">cytoplasm<\/strong>.<\/p>\n<p id=\"gob-ch17_s05_p07\" class=\"para\">Most lipids can be saponified, but some, such as <strong class=\"emphasis bold\">steroids<\/strong>, cannot be saponified. The steroid <strong class=\"emphasis bold\">cholesterol<\/strong> is found in animal cells but not in appreciable quantities in plant cells. It is a main component of all animal cell membranes and a precursor for hormones, vitamin D, and bile salts. Bile salts are the most important constituents of <strong class=\"emphasis bold\">bile<\/strong>, which is a yellowish-green liquid secreted by the gallbladder into the small intestine and is needed for the proper digestion of lipids.<\/p>\n<\/div>\n<\/div>\n<div class=\"textbox exercises\">\n<div id=\"gob-ch17_s05_n01\" class=\"callout editable block\">\n<h3 class=\"title\">Additional Exercises<\/h3>\n<\/div>\n<div id=\"gob-ch17_s05_qs01\" class=\"qandaset block\">\n<ol id=\"gob-ch17_s05_qs01_qd01\" class=\"qandadiv\">\n<li id=\"gob-ch17_s05_qs01_qd01_qa01\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p01\" class=\"para\">The melting point of elaidic acid is 52\u00b0C.<\/p>\n<ol id=\"gob-ch17_s05_qs01_l01\" class=\"orderedlist\">\n<li>What trend is observed when comparing the melting points of elaidic acid, oleic acid, and stearic acid? Explain.<\/li>\n<li>\n<p class=\"para\">Would you expect the melting point of palmitelaidic acid to be lower or higher than that of elaidic acid? Explain.<\/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\/21161109\/0270c4c45ab6484444b6fed4ac626491.jpg\" alt=\"image\" \/><\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa02\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p02\" class=\"para\">Examine the labels on two brands of margarine and two brands of shortening and list the oils used in the various brands.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa03\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p04\" class=\"para\">Draw a typical lecithin molecule that incorporates glycerol, palmitic acid, oleic acid, phosphoric acid, and choline. Circle all the ester bonds.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa04\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p05\" class=\"para\">In cerebrosides, is the linkage between the fatty acid and sphingosine an amide bond or an ester bond? Justify your answer.<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa05\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p07\" class=\"para\">Serine is an amino acid that has the following structure. Draw the structure for a phosphatidylserine that contains a palmitic acid and a palmitoleic acid unit.<\/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\/21161113\/d6337e89bff3a69089a0fe5e9eb01a8a.jpg\" alt=\"image\" \/><\/div>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa06\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p08\" class=\"para\">Explain whether each compound would be expected to diffuse through the lipid bilayer of a cell membrane.<\/p>\n<ol id=\"gob-ch17_s05_qs01_l03\" class=\"orderedlist\">\n<li>potassium chloride<\/li>\n<li>CH<sub class=\"subscript\">3<\/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>CH<sub class=\"subscript\">3<\/sub><\/li>\n<li>fructose<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa07\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p09\" class=\"para\">Identify the role of each steroid hormone in the body.<\/p>\n<ol id=\"gob-ch17_s05_qs01_l05\" class=\"orderedlist\">\n<li>progesterone<\/li>\n<li>aldosterone<\/li>\n<li>testosterone<\/li>\n<li>cortisol<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa08\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p10\" class=\"para\">How does the structure of cholic acid differ from that of cholesterol? Which compound would you expect to be more polar? Why?<\/p>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa09\" class=\"qandaentry\">\n<div class=\"question\">\n<ol id=\"gob-ch17_s05_qs01_l07\" class=\"orderedlist\">\n<li>What fatty acid is the precursor for the prostaglandins?<\/li>\n<li>Identify three biological effects of prostaglandins.<\/li>\n<\/ol>\n<\/div>\n<\/li>\n<li id=\"gob-ch17_s05_qs01_qd01_qa10\" class=\"qandaentry\">\n<div class=\"question\">\n<p id=\"gob-ch17_s05_qs01_p13\" class=\"para\">Why is it important to determine the ratio of LDLs to HDLs, rather than just the concentration of serum cholesterol?<\/p>\n<\/div>\n<\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"gob-ch17_s05_qs01_ans\" class=\"qandaset block\">\n<div class=\"answer\">\n<div class=\"textbox exercises\">\n<h3>Answers<\/h3>\n<div class=\"qa-wrapper\" style=\"display: block\"><span class=\"show-answer collapsed\" style=\"cursor: pointer\" data-target=\"q268154\">Show Answer<\/span><\/p>\n<div id=\"q268154\" class=\"hidden-answer\" style=\"display: none\">\n<p>1. a. Stearic acid has the highest melting point, followed by elaidic acid, and then oleic acid with the lowest melting point. Elaidic acid is a <em class=\"emphasis\">trans<\/em> fatty acid, and the carbon chains can pack together almost as tightly as those of the saturated stearic acid. Oleic acid is a <em class=\"emphasis\">cis<\/em> fatty acid, and the bend in the hydrocarbon chain keeps these carbon chains from packing as closely together; fewer interactions lead to a much lower melting point.<\/p>\n<p>b. The melting point of palmitelaidic acid should be lower than that of elaidic acid because it has a shorter carbon chain (16, as compared to 18 for elaidic acid). The shorter the carbon chain, the lower the melting point due to a decrease in intermolecular interactions, assuming other factors such as the number of carbon-to-carbon double bonds is the same.<\/p>\n<div class=\"answer\"><\/div>\n<div class=\"answer\">\n<div class=\"informalfigure large\">3.<img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21161123\/2f72b31967541a6516059225e6511ef1.jpg\" alt=\"image\" \/><\/div>\n<\/div>\n<div class=\"answer\"><\/div>\n<div class=\"answer\">\n<div class=\"informalfigure large\">5.\u00a0<img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3101\/2018\/03\/21161130\/39f11c5526ff31b33f7a95b80db827e1.jpg\" alt=\"image\" \/><\/div>\n<\/div>\n<div class=\"answer\"><\/div>\n<div class=\"answer\">\n<p>7. a. regulates the menstrual cycle and maintains pregnancy<\/p>\n<p>b. regulates salt metabolism by stimulating the kidneys to retain sodium and excrete potassium<\/p>\n<p>c. stimulates and maintains male sex characteristics<\/p>\n<p>d. stimulates the conversion of proteins to carbohydrates<\/p>\n<\/div>\n<div class=\"answer\"><\/div>\n<div class=\"answer\">\n<p>9. a. arachidonic acid<\/p>\n<p>b. induce smooth muscle contraction, lower blood pressure, and contribute to the inflammatory response\u00a0<\/p><\/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-1948\">\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":10,"template":"","meta":{"_candela_citation":"[{\"type\":\"cc\",\"description\":\"The Basics of General, Organic, and Biological Chemistry v. 1.0\",\"author\":\"\",\"organization\":\"Saylor 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