Chapter 4: Q40 P (page 166)
The stereoisomer of cholesterol found in nature is shown here.
a. How many asymmetric centers does cholesterol have?
b. What is the maximum number of stereoisomers that cholesterol can have?
Short Answer
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Chapter 4: Q40 P (page 166)
The stereoisomer of cholesterol found in nature is shown here.
a. How many asymmetric centers does cholesterol have?
b. What is the maximum number of stereoisomers that cholesterol can have?
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Naproxen, a nonsteroidal anti-inflammatory drug that is the active ingredient in Aleve (p. 115), has a specific rotation of +66. One commercial preparation result in a mixture with a 97% enantiomeric excess.
a. Does naproxen have the R or the S configuration?
b. What percent of each enantiomer is obtained from the commercial preparation?
Are the following pairs identical, enantiomers, diastereomers, or constitutional isomers?


Draw a perspective formula for each of the following:
a. (S)-2-chlorobutane
b. (R)-1,2-dibromobutane
Which of the following are optically active?

Draw the Z isomer of an alkene that has a CH3and an H on one sp2carbon and isopropyl and butyl groups on the othersp2carbon.
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