Chapter 4: Q41 P (page 166)
Draw the stereoisomers of the following amino acids. Indicate pairs of enantiomers and pairs of diastereomers.
Short Answer
- 2 stereoisomers- S and R
- 4 stereoisomers- RR, SS, RS and SR.
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Chapter 4: Q41 P (page 166)
Draw the stereoisomers of the following amino acids. Indicate pairs of enantiomers and pairs of diastereomers.
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Draw all possible stereoisomers for each of the following. Indicate those compounds for which no stereoisomers are possible.
a. 1-bromo-2-chlorocyclohexane
b. 2-bromo-4-methylpentane
c. 1,2-dichlorocyclohexane
d. 2-bromo-4-chloropentane
e. 1-bromo-4-chlorocyclohexane
f. 1,2-dimethylcyclopropane
g. 4-bromo-2-pentene
h. 3,3-dimethylpentane
i. 1-bromo-2-chlorocyclobutane
j. 1-bromo-3-chlorocyclobutane
a. Using the wedge-and-dash notation, draw the nine stereoisomers of 1,2,3,4,5,6-hexachlorocyclohexane.
b. From the nine stereoisomers, identify one pair of enantiomers.
c. Draw the most stable conformer of the most stable stereoisomer.
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?
Mevacor is used clinically to lower serum cholesterol levels. How many asymmetric centers does Mevacor have?

What is the configuration of each of the asymmetric centers in the following compounds?
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