Which one of the following structures represents a
meso compound?
A)

D)

B)

E)

C)
Question 2
represents
A)
(2
R,3
R)-2,3-butanediol.
B)
(2
S,3
S)-2,3-butanediol.
C)
the most stable conformer of (2
R,3
R)-2,3-butanediol.
D)
the least stable conformer of (2
R,3
R)-2,3-butanediol.
E)
meso-2,3-butanediol.
Question 3The Fischer projection that represents the same molecule as

is:
A)

D)

B)

E)

C)
Question 4The Fischer projection formula for (
S)-lactic acid (2-hydroxypropanoic acid) is
A)

D)

B)

E)

C)
Question 5The absolute configuration around the stereogenic center of the molecule below is:
A)
R B)
S C)
E D)
Z E)
transQuestion 6What is the absolute configuration around C-2 and C-3?
A)
R, R B)
S, S C)
R, S D)
S, R E)
E, ZQuestion 7What is correct name for the following structure?
A)
(
R,S)-2,3-dichlorobutane
B)
(2
R,3
S)-2,3-dichlorobutane
C)
(2
S,3
S)-2,3-dichlorobutane
D)
(2
R,3
R)-2,3-dichlorobutane
E)
none of these
Question 8Which name describes the following structure?
A)
(R)-4-methyl-1-hexen-4-ol
B)
(S)-4-ethyl-1-penten-4-ol
C)
(R)-4-ethyl-1-penten-3-ol
D)
(S)-4-methyl-1-hexen-4-ol
E)
(S)-4-methyl-1-hexyn-4-ol
Question 9Which name describes the following structure?
A)
(R)-3-methyl-1-penten-3-ol
B)
(S)-3-methyl-1-penten-3-ol
C)
(R)-3-ethyl-1-buten-3-ol
D)
(R)-3-methyl-1-pentyn-3-ol
E)
(S)-3-ethyl-1-buten-3-ol
Question 10The priority order for R/S nomenclature is
A)
CH=CH
2 > OH > CH
3 > CH
2CH
3 B)
OH > CH
2CH
3 > CH=CH
2 > CH
3 C)
OH > CH=CH
2 > CH
2CH
3 > CH
3 D)
CH
3 > CH
2CH
3 > CH=CH
2 > OH
E)
CH
2CH
3 > CH
3 > CH=CH
2 > OH