PROBLEM 30
Chloramphenicol is a broad-spectrum antibiotic that is particularly useful against typhoid
fever. What is the configuration of each asymmetric carbon in chloramphenicol?
chloramphenicol
NHCCHCl 2
HO H
H CC
O
NO 2
CH 2 OH
206 CHAPTER 5 Stereochemistry
Notice that enantiomers have the opposite configuration at both asymmetric carbons,
whereas diastereomers have the same configuration at one asymmetric carbon and the
opposite configuration at the other.
PROBLEM 29
Draw and name the four stereoisomers of 1,3-dichloro-2-butanol using:
a. perspective formulas b. Fischer projections
Tartaric acid has three stereoisomers because each of its two asymmetric carbons
has the same set of four substituents. The meso compound and the pair of enantiomers
are named as shown.
The physical properties of the three stereoisomers of tartaric acid are listed in
Table 5.1. The meso compound and either one of the enantiomers are diastereomers.
Notice that the physical properties of the enantiomers are the same, whereas the phys-
ical properties of the diastereomers are different. Also notice that the physical proper-
ties of the racemic mixture differ from the physical properties of the enantiomers.
(2R,3S)-tartaric acid
a meso compound
(2R,3R)-tartaric acid
a pair of enantiomers
a pair of enantiomers
Fischer projections of the stereoisomers of tartaric acid
(2S,3S)-tartaric acid
COOH
COOH
OH
H OH
H
COOH
COOH
OH
HO H
H
COOH
COOH
H
H OH
(^2323) HO (^23)
(2R,3S)-tartaric acid
a meso compound
HOOC
H
HO
H
OH
COOH
C C
(2R,3R)-tartaric acid
perspective formulas of the stereoisomers of tartaric acid
HOOC
H
HO
OH
H
COOH
C C
(2S,3S)-tartaric acid
H
HO
HOOC
H
COOH
OH
C C
22333 2
Tutorial:
Identification of stereoisomers
with multiple asymmetric
carbons
Table 5.1 Physical Properties of the Stereoisomers of Tartaric Acid
Melting Solubility,
point, °C at 15 °C
(2R,3R)- acid 170 139
(2S,3S)- acid 170 139
(2R,3S)-Tartaric acid 140 0 ° 125
(;)-Tartaricacid 206 0 ° 139
(-)-Tartaric -11.98°
(+)-Tartaric +11.98°
[A]^25 D°C g/100 g H 2 O