Chapter 31: Q15P (page 1253)
Draw the enantiomer and any two diastereomers of cholesterol. Does the OH group of cholesterol occupy an axial or equatorial position?
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Chapter 31: Q15P (page 1253)
Draw the enantiomer and any two diastereomers of cholesterol. Does the OH group of cholesterol occupy an axial or equatorial position?
Answer

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Why are phospholipids, but not triacylglycerols, found in cell membranes?
How would you expect the melting point of eicosapentaenoic acid to compare with the melting points of the fatty acids listed in Table 31.2?
Locate the isoprene units in each compound.
(a)
(b)

(c)

(d)

(e)
(f)

(g)

(h)

(a) Draw a skeletal structure of the anabolic steroid methenolone from the following description. Methenolone contains the tetracyclic steroid skeleton with a carbonyl group at C3, a hydroxyl group at C17, a double bond between C1 and C2, and methyl groups bonded to C1, C10 and C13. (b) Add wedges and dashed wedges for all stereogenic centers with the following information: The configuration at C10 is R, The configuration at C13 is S, the configuration at C17 is S, and all substitutents at ring fusions are trans to each other. (c) Draw the structures of Primobolan, the product formed when methenolone is treated with and pyridine. Primobolan is an anabolic steroid that can be taken orally or by injection and has been used illegally by well-known Major League Baseball players.
Triacylglycerol L yields compound M when treated with excess H2 , Pd-C. Ozonolysis of L [1] O3 ; [2] affords compounds N-P. What is the structure of L?




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