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Of the following structures, how many are classified "E"? Of the following structures, how many are classified  E ?     A)  1 B)  2 C)  3 D)  4 E)  5 Of the following structures, how many are classified  E ?     A)  1 B)  2 C)  3 D)  4 E)  5


A) 1
B) 2
C) 3
D) 4
E) 5

F) A) and B)
G) D) and E)

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The terms that best describe the isomeric relationship between staggered and eclipsed ethane are


A) configurational, achiral, diastereomers.
B) conformational, chiral, enantiomers.
C) conformational, achiral, diastereomers.
D) configurational, chiral, enantiomers.
E) conformational, achiral, enantiomers.

F) B) and E)
G) A) and C)

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C

An unknown sample is tested with a polarimeter for optical activity.The results of the test require movement of the analyzer.What samples would give this result?


A) pure enantiomer
B) meso compound
C) racemic mixture
D) both B and C
E) none of these

F) All of the above
G) A) and C)

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The number of stereogenic centers in progesterone is: The number of stereogenic centers in progesterone is:   progesterone (no stereochemistry shown)  A)  2 B)  3 C)  4 D)  5 E)  6 progesterone (no stereochemistry shown)


A) 2
B) 3
C) 4
D) 5
E) 6

F) B) and D)
G) A) and E)

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Which of the following structures is (E) -2,3-dichloro-2-pentene? Which of the following structures is (E) -2,3-dichloro-2-pentene?     A)  1 B)  2 C)  3 D)  4 E)  5 Which of the following structures is (E) -2,3-dichloro-2-pentene?     A)  1 B)  2 C)  3 D)  4 E)  5


A) 1
B) 2
C) 3
D) 4
E) 5

F) None of the above
G) A) and E)

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E

According to the R-S convention, which priority is correct for the following sets of groups?


A) NH2 > Cl > CH3 > H
B) Cl > NH2 > CH3 > H
C) Cl > CH3 > NH2 > H
D) H > Cl > CH3 > NH2
E) CH3 > NH2 > Cl > H

F) C) and D)
G) A) and E)

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The total number of possible stereoisomers of The total number of possible stereoisomers of   is: A)  2 B)  4 C)  6 D)  8 E)  0 is:


A) 2
B) 4
C) 6
D) 8
E) 0

F) B) and D)
G) All of the above

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The terms that best describe the relationship between (2R,3S) -2,3-butanediol and (2S,3S) -2,3-butanediol are


A) configurational, diastereomers.
B) conformational, enantiomers.
C) conformational, diastereomers
D) configurational, enantiomers.
E) configurational, cis/trans.

F) None of the above
G) A) and D)

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Of the following structures, how many are classified "Z"? Of the following structures, how many are classified  Z ?     A)  1 B)  2 C)  3 D)  4 E)  5 Of the following structures, how many are classified  Z ?     A)  1 B)  2 C)  3 D)  4 E)  5


A) 1
B) 2
C) 3
D) 4
E) 5

F) A) and D)
G) A) and C)

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When (R) -3-bromo-2-methyl-1-butene is reacted with HBr, two stereoisomers are formed.What is the relationship of these stereoisomers?


A) enantiomers
B) meso compounds
C) diastereomers
D) E
E) Z

F) None of the above
G) B) and C)

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The total number of possible stereoisomers of 1-bromo-2-chlorocyclopentane is:


A) 2
B) 4
C) 6
D) 8
E) 0

F) None of the above
G) A) and B)

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B

The Fischer projection that represents the same molecule as The Fischer projection that represents the same molecule as   is: A)    B)    C)    D)    E)   is:


A) The Fischer projection that represents the same molecule as   is: A)    B)    C)    D)    E)
B) The Fischer projection that represents the same molecule as   is: A)    B)    C)    D)    E)
C) The Fischer projection that represents the same molecule as   is: A)    B)    C)    D)    E)
D) The Fischer projection that represents the same molecule as   is: A)    B)    C)    D)    E)
E) The Fischer projection that represents the same molecule as   is: A)    B)    C)    D)    E)

F) A) and C)
G) A) and E)

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Which of the following structures depicts (R) -3-ethyl-2,3-dimethylhexane?


A) Which of the following structures depicts (R) -3-ethyl-2,3-dimethylhexane? A)    B)    C)    D)    E)
B) Which of the following structures depicts (R) -3-ethyl-2,3-dimethylhexane? A)    B)    C)    D)    E)
C) Which of the following structures depicts (R) -3-ethyl-2,3-dimethylhexane? A)    B)    C)    D)    E)
D) Which of the following structures depicts (R) -3-ethyl-2,3-dimethylhexane? A)    B)    C)    D)    E)
E) Which of the following structures depicts (R) -3-ethyl-2,3-dimethylhexane? A)    B)    C)    D)    E)

F) A) and D)
G) B) and E)

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A 50:50 mixture of enantiomers


A) is a meso form.
B) is a pair of diastereomers.
C) is a racemic mixture.
D) rotates plane polarized light.
E) is a pair of conformers.

F) A) and C)
G) C) and D)

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Which name describes the following structure? Which 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


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

F) A) and D)
G) B) and E)

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How many stereogenic carbons are produced from the following sequence of reactions? How many stereogenic carbons are produced from the following sequence of reactions?   A)  1 B)  2 C)  3 D)  4 E)  5


A) 1
B) 2
C) 3
D) 4
E) 5

F) A) and C)
G) A) and D)

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An unknown sample is tested with a polarimeter for optical activity.The results of the test required no movement of the analyzer.What samples would give this result?


A) pure enantiomer
B) meso compound
C) racemic mixture
D) both B and C
E) none of these

F) D) and E)
G) None of the above

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What is correct name for the following structure? What is correct name for the following structure?   A)  (R,S) -2,3-dichlorobutane B)  (2R,3S) -2,3-dichlorobutane C)  (2S,3S) -2,3-dichlorobutane D)  (2R,3R) -2,3-dichlorobutane E)  none of these


A) (R,S) -2,3-dichlorobutane
B) (2R,3S) -2,3-dichlorobutane
C) (2S,3S) -2,3-dichlorobutane
D) (2R,3R) -2,3-dichlorobutane
E) none of these

F) C) and E)
G) A) and E)

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How many stereogenic centers are present in the following molecule? How many stereogenic centers are present in the following molecule?   A)  1 B)  2 C)  3 D)  4 E)  5


A) 1
B) 2
C) 3
D) 4
E) 5

F) A) and B)
G) A) and E)

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The Fischer projection formula for (S) -lactic acid (2-hydroxypropanoic acid) is


A) The Fischer projection formula for (S) -lactic acid (2-hydroxypropanoic acid)  is A)    B)    C)    D)    E)
B) The Fischer projection formula for (S) -lactic acid (2-hydroxypropanoic acid)  is A)    B)    C)    D)    E)
C) The Fischer projection formula for (S) -lactic acid (2-hydroxypropanoic acid)  is A)    B)    C)    D)    E)
D) The Fischer projection formula for (S) -lactic acid (2-hydroxypropanoic acid)  is A)    B)    C)    D)    E)
E) The Fischer projection formula for (S) -lactic acid (2-hydroxypropanoic acid)  is A)    B)    C)    D)    E)

F) All of the above
G) None of the above

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