Deck 6: Chirality: the Handedness of Molecules

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Question
Rank the following substituents in order of decreasing priority (highest first).
<strong>Rank the following substituents in order of decreasing priority (highest first).  </strong> A) II, III, IV, I B) III, IV, I, II C) IV, III, II, I D) IV, I, II, III <div style=padding-top: 35px>

A) II, III, IV, I
B) III, IV, I, II
C) IV, III, II, I
D) IV, I, II, III
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Question
Which structure is correctly named 3S,4S-3,4-dimethylhexane ?
<strong>Which structure is correctly named 3S,4S-3,4-dimethylhexane ?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Which structures are chiral?
<strong>Which structures are chiral?  </strong> A) I, II, V B) I, II C) II, II, IV D) III, IV <div style=padding-top: 35px>

A) I, II, V
B) I, II
C) II, II, IV
D) III, IV
Question
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers <div style=padding-top: 35px>

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
Question
Which forms of lactic acid are R forms?
<strong>Which forms of lactic acid are R forms?  </strong> A) I, II B) III, IV C) II, III D) I, IV <div style=padding-top: 35px>

A) I, II
B) III, IV
C) II, III
D) I, IV
Question
Rank the following substituents in order of increasing priority.
<strong>Rank the following substituents in order of increasing priority.  </strong> A) III, II, IV, I B) I, IV, II, III C) IV, I, III, II D) I, II, III, IV <div style=padding-top: 35px>

A) III, II, IV, I
B) I, IV, II, III
C) IV, I, III, II
D) I, II, III, IV
Question
Rank the following substituents in order of increasing priority.
<strong>Rank the following substituents in order of increasing priority.  </strong> A) III, II, IV, I B) IV, I, II, III C) III, I, II, IV D) IV, II, I, III <div style=padding-top: 35px>

A) III, II, IV, I
B) IV, I, II, III
C) III, I, II, IV
D) IV, II, I, III
Question
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers <div style=padding-top: 35px>

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
Question
Which compounds contain stereocenters?
<strong>Which compounds contain stereocenters?  </strong> A) I, II B) III, IV C) I, III D) II, IV <div style=padding-top: 35px>

A) I, II
B) III, IV
C) I, III
D) II, IV
Question
Rank the following substituents in order of increasing priority.
<strong>Rank the following substituents in order of increasing priority.  </strong> A) I, III, II, IV B) II, I, III, IV C) III, I, II, IV D) IV, III, I, II <div style=padding-top: 35px>

A) I, III, II, IV
B) II, I, III, IV
C) III, I, II, IV
D) IV, III, I, II
Question
How many stereoisomers are possible for 1,2-dichlorocyclopentane?

A) 1
B) 2
C) 3
D) 4
Question
Which pair of structures are enantiomers?
<strong>Which pair of structures are enantiomers?  </strong> A) I, II B) II, III C) I, III D) I, II, III <div style=padding-top: 35px>

A) I, II
B) II, III
C) I, III
D) I, II, III
Question
Which structures represent R-3-methylhexane?
Help: Build the structures using a molecular model.
<strong>Which structures represent R-3-methylhexane? Help: Build the structures using a molecular model.  </strong> A) III, IV B) I, II C) I, III D) II, IV <div style=padding-top: 35px>

A) III, IV
B) I, II
C) I, III
D) II, IV
Question
What is the R,S configuration for the following structure of isocitric acid?
<strong>What is the R,S configuration for the following structure of isocitric acid?  </strong> A) 2R, 3R B) 2R, 3S C) 2S, 3R D) 2S, 3S <div style=padding-top: 35px>

A) 2R, 3R
B) 2R, 3S
C) 2S, 3R
D) 2S, 3S
Question
Aspartame is an artificial, non-saccharide sweetener. It is made from two amino acids: phenylalanine (methyl ester) and aspartic acid. Both aminoacids have one stereocenter. Both stereocenters have S-stereoconfiguration. Which of the two structures is aspartame?
<strong>Aspartame is an artificial, non-saccharide sweetener. It is made from two amino acids: phenylalanine (methyl ester) and aspartic acid. Both aminoacids have one stereocenter. Both stereocenters have S-stereoconfiguration. Which of the two structures is aspartame?  </strong> A) both structures are correct B) I C) II D) Neither structure is correct. <div style=padding-top: 35px>

A) both structures are correct
B) I
C) II
D) Neither structure is correct.
Question
Which compounds contain stereocenters?
I. 1-chloropentane
II. 2-chloropentane
III. 3-chloropentane
IV. 1,2-dichloropentane

A) I, II
B) III, IV
C) I, III
D) II, IV
Question
Which compounds have multiple stereocenters?
<strong>Which compounds have multiple stereocenters?  </strong> A) I, II B) III, IV C) II, III D) I, III <div style=padding-top: 35px>

A) I, II
B) III, IV
C) II, III
D) I, III
Question
How many stereoisomers are possible for 2,3-butanediol?

A) 1
B) 2
C) 3
D) 4
Question
How many stereoisomers are possible for the following structure?
<strong>How many stereoisomers are possible for the following structure?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which compounds contain stereocenters?
I. 2-methylpentane
II. chlorocyclohexane
III. 3-methyl-2-butanol
IV. 2-hydroxypropanoic acid

A) I, II
B) III, IV
C) I, III
D) II, IV
Question
Which statements about stereoisomers are true? (Sec. 6.7, 6.8)
I. enantiomers and diastereomers have the same physical properties.
II. 50/50 mixtures of R and S enantiomers are called racemic mixtures.
III. meso isomers rotate the plane of plane polarized light.
IV. dextrorotatory compounds rotate plane polarized light to the right.

A) I, II
B) II, III
C) II, IV
D) III, IV
Question
The specific rotation of dextrorotatory tartaric acid is +12.7 degrees. A mixture of dextrorotatory and levorotatory tartaric acid has a specific rotation of +6.35 degrees. What is the optical purity of the mixture?

A) 25%
B) 33 1/3%
C) 50%
D) 75%
Question
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers <div style=padding-top: 35px>

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
Question
What is the relationship between these two structures?
HINT: Build the molecular models and compare!
<strong>What is the relationship between these two structures? HINT: Build the molecular models and compare!  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers <div style=padding-top: 35px>

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
Question
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) identical structures B) enantiomers C) diastereomers D) constitutional isomers <div style=padding-top: 35px>

A) identical structures
B) enantiomers
C) diastereomers
D) constitutional isomers
Question
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers <div style=padding-top: 35px>

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
Question
The priority order for the following groups are (highest = 1),
The priority order for the following groups are (highest = 1),  <div style=padding-top: 35px>
Question
The priority order for the following groups is (highest = 1),
The priority order for the following groups is (highest = 1),  <div style=padding-top: 35px>
Question
Which statement about enantiomers is false?

A) enantiomers have the same boiling and melting points.
B) enantiomers have the same chemical properties in an achiral environment.
C) enantiomers have the same atom connectivity.
D) enantiomers have the same three dimensional orientation.
Question
Which are meso compounds?
<strong>Which are meso compounds?  </strong> A) I and II B) II and III C) I and III D) III and IV <div style=padding-top: 35px>

A) I and II
B) II and III
C) I and III
D) III and IV
Question
Which are meso compounds?
<strong>Which are meso compounds?  </strong> A) I, II B) I, III C) II, III D) III, IV <div style=padding-top: 35px>

A) I, II
B) I, III
C) II, III
D) III, IV
Question
How many stereoisomers are possible for Prilosec?
<strong>How many stereoisomers are possible for Prilosec?  </strong> A) 0 B) 2 C) 4 D) 8 <div style=padding-top: 35px>

A) 0
B) 2
C) 4
D) 8
Question
Which are meso compounds?
<strong>Which are meso compounds?  </strong> A) I and II B) II and III C) I and III D) II and IV <div style=padding-top: 35px>

A) I and II
B) II and III
C) I and III
D) II and IV
Question
The structure of the S,S enantiomer of 2,3-butanediol is,
The structure of the S,S enantiomer of 2,3-butanediol is,  <div style=padding-top: 35px>
Question
Tuftsin (named after Tufts University) has important functions in the human immune system. It binds to stereospecific receptors at the surface of macrophages and leukocytes, stimulating their bactericidal and tumoricidal activity. All stereocenters in this molecule have S-configurations. How many stereoisomers of tuftsin exist, which do not have the correct stereochemistry for receptor-binding?
<strong>Tuftsin (named after Tufts University) has important functions in the human immune system. It binds to stereospecific receptors at the surface of macrophages and leukocytes, stimulating their bactericidal and tumoricidal activity. All stereocenters in this molecule have S-configurations. How many stereoisomers of tuftsin exist, which do not have the correct stereochemistry for receptor-binding?  </strong> A) 7 B) 15 C) 31 D) 32 <div style=padding-top: 35px>

A) 7
B) 15
C) 31
D) 32
Question
The following structure is the _____________ configuration.
The following structure is the _____________ configuration.  <div style=padding-top: 35px>
Question
How many pairs of enantiomers are possible for cholesterol?
<strong>How many pairs of enantiomers are possible for cholesterol?  </strong> A) 16 B) 32 C) 64 D) 128 <div style=padding-top: 35px>

A) 16
B) 32
C) 64
D) 128
Question
Which compound is a meso compound?
<strong>Which compound is a meso compound?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
The following structure is the _____________ configuration.
The following structure is the _____________ configuration.  <div style=padding-top: 35px>
Question
How many pairs of enantiomers are possible for cortisone acetate?
<strong>How many pairs of enantiomers are possible for cortisone acetate?  </strong> A) 32 B) 64 C) 128 D) 256 <div style=padding-top: 35px>

A) 32
B) 64
C) 128
D) 256
Question
Hydrocodone, the synthetic opiate in Vicodin contains ______ stereocenters.
Hydrocodone, the synthetic opiate in Vicodin contains ______ stereocenters.  <div style=padding-top: 35px>
Question
The structure of the 3S,4R enantiomer of 3-bromo-4-chlorohexane is,
The structure of the 3S,4R enantiomer of 3-bromo-4-chlorohexane is,  <div style=padding-top: 35px>
Question
The following structure contains ………..stereocenters.
The following structure contains ………..stereocenters.  <div style=padding-top: 35px>
Question
The following structure contains ___________ stereocenters.
The following structure contains ___________ stereocenters.  <div style=padding-top: 35px>
Question
The following structures are diastereomers.
The following structures are diastereomers.  <div style=padding-top: 35px>
Question
2R,4R-2-bromo-4-chloropentane and 2S,4S-2-bromo-4-chloropentane are meso compounds.
Question
Enantiomers have the same physical properties (m.p., b.p., density).
Question
Glutathione is an antioxidant, which helps to protect our cells from oxidative damage. Assign R or S configurations to the stereocenters I and II
Glutathione is an antioxidant, which helps to protect our cells from oxidative damage. Assign R or S configurations to the stereocenters I and II  <div style=padding-top: 35px>
Question
The following structure contains??____stereocenters.
The following structure contains??____stereocenters.  <div style=padding-top: 35px>
Question
The following structures are enantiomers.
The following structures are enantiomers.  <div style=padding-top: 35px>
Question
The diastereomer of 2R,3R-dichlorobutane is achiral.
Question
The name of the following structure is 2S,3S-2,3-dibromobutane.
The name of the following structure is 2S,3S-2,3-dibromobutane.  <div style=padding-top: 35px>
Question
Meso compounds rotate plane polarized light the same magnitude as enantiomers, but in opposite directions.
Question
The following structure contains __________ stereocenters.
The following structure contains __________ stereocenters.  <div style=padding-top: 35px>
Question
The following groups are listed in decreasing order of priority.
The following groups are listed in decreasing order of priority.  <div style=padding-top: 35px>
Question
The following groups are listed in decreasing order of priority.
The following groups are listed in decreasing order of priority.  <div style=padding-top: 35px>
Question
The following structures are __________________ (what type of stereoisomer?).
The following structures are __________________ (what type of stereoisomer?).  <div style=padding-top: 35px>
Question
The following structures are ________________ (what type of stereoisomer).
The following structures are ________________ (what type of stereoisomer).  <div style=padding-top: 35px>
Question
The diastereomers 2S,4R-2-bromo-4-chloropentane and 2S,4S-2-bromo-4-chloropentane are achiral.
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Deck 6: Chirality: the Handedness of Molecules
1
Rank the following substituents in order of decreasing priority (highest first).
<strong>Rank the following substituents in order of decreasing priority (highest first).  </strong> A) II, III, IV, I B) III, IV, I, II C) IV, III, II, I D) IV, I, II, III

A) II, III, IV, I
B) III, IV, I, II
C) IV, III, II, I
D) IV, I, II, III
IV, I, II, III
2
Which structure is correctly named 3S,4S-3,4-dimethylhexane ?
<strong>Which structure is correctly named 3S,4S-3,4-dimethylhexane ?  </strong> A) I B) II C) III D) IV

A) I
B) II
C) III
D) IV
IV
3
Which structures are chiral?
<strong>Which structures are chiral?  </strong> A) I, II, V B) I, II C) II, II, IV D) III, IV

A) I, II, V
B) I, II
C) II, II, IV
D) III, IV
III, IV
4
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
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5
Which forms of lactic acid are R forms?
<strong>Which forms of lactic acid are R forms?  </strong> A) I, II B) III, IV C) II, III D) I, IV

A) I, II
B) III, IV
C) II, III
D) I, IV
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6
Rank the following substituents in order of increasing priority.
<strong>Rank the following substituents in order of increasing priority.  </strong> A) III, II, IV, I B) I, IV, II, III C) IV, I, III, II D) I, II, III, IV

A) III, II, IV, I
B) I, IV, II, III
C) IV, I, III, II
D) I, II, III, IV
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7
Rank the following substituents in order of increasing priority.
<strong>Rank the following substituents in order of increasing priority.  </strong> A) III, II, IV, I B) IV, I, II, III C) III, I, II, IV D) IV, II, I, III

A) III, II, IV, I
B) IV, I, II, III
C) III, I, II, IV
D) IV, II, I, III
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8
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
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9
Which compounds contain stereocenters?
<strong>Which compounds contain stereocenters?  </strong> A) I, II B) III, IV C) I, III D) II, IV

A) I, II
B) III, IV
C) I, III
D) II, IV
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10
Rank the following substituents in order of increasing priority.
<strong>Rank the following substituents in order of increasing priority.  </strong> A) I, III, II, IV B) II, I, III, IV C) III, I, II, IV D) IV, III, I, II

A) I, III, II, IV
B) II, I, III, IV
C) III, I, II, IV
D) IV, III, I, II
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11
How many stereoisomers are possible for 1,2-dichlorocyclopentane?

A) 1
B) 2
C) 3
D) 4
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12
Which pair of structures are enantiomers?
<strong>Which pair of structures are enantiomers?  </strong> A) I, II B) II, III C) I, III D) I, II, III

A) I, II
B) II, III
C) I, III
D) I, II, III
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13
Which structures represent R-3-methylhexane?
Help: Build the structures using a molecular model.
<strong>Which structures represent R-3-methylhexane? Help: Build the structures using a molecular model.  </strong> A) III, IV B) I, II C) I, III D) II, IV

A) III, IV
B) I, II
C) I, III
D) II, IV
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14
What is the R,S configuration for the following structure of isocitric acid?
<strong>What is the R,S configuration for the following structure of isocitric acid?  </strong> A) 2R, 3R B) 2R, 3S C) 2S, 3R D) 2S, 3S

A) 2R, 3R
B) 2R, 3S
C) 2S, 3R
D) 2S, 3S
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15
Aspartame is an artificial, non-saccharide sweetener. It is made from two amino acids: phenylalanine (methyl ester) and aspartic acid. Both aminoacids have one stereocenter. Both stereocenters have S-stereoconfiguration. Which of the two structures is aspartame?
<strong>Aspartame is an artificial, non-saccharide sweetener. It is made from two amino acids: phenylalanine (methyl ester) and aspartic acid. Both aminoacids have one stereocenter. Both stereocenters have S-stereoconfiguration. Which of the two structures is aspartame?  </strong> A) both structures are correct B) I C) II D) Neither structure is correct.

A) both structures are correct
B) I
C) II
D) Neither structure is correct.
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16
Which compounds contain stereocenters?
I. 1-chloropentane
II. 2-chloropentane
III. 3-chloropentane
IV. 1,2-dichloropentane

A) I, II
B) III, IV
C) I, III
D) II, IV
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17
Which compounds have multiple stereocenters?
<strong>Which compounds have multiple stereocenters?  </strong> A) I, II B) III, IV C) II, III D) I, III

A) I, II
B) III, IV
C) II, III
D) I, III
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18
How many stereoisomers are possible for 2,3-butanediol?

A) 1
B) 2
C) 3
D) 4
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19
How many stereoisomers are possible for the following structure?
<strong>How many stereoisomers are possible for the following structure?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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20
Which compounds contain stereocenters?
I. 2-methylpentane
II. chlorocyclohexane
III. 3-methyl-2-butanol
IV. 2-hydroxypropanoic acid

A) I, II
B) III, IV
C) I, III
D) II, IV
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21
Which statements about stereoisomers are true? (Sec. 6.7, 6.8)
I. enantiomers and diastereomers have the same physical properties.
II. 50/50 mixtures of R and S enantiomers are called racemic mixtures.
III. meso isomers rotate the plane of plane polarized light.
IV. dextrorotatory compounds rotate plane polarized light to the right.

A) I, II
B) II, III
C) II, IV
D) III, IV
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22
The specific rotation of dextrorotatory tartaric acid is +12.7 degrees. A mixture of dextrorotatory and levorotatory tartaric acid has a specific rotation of +6.35 degrees. What is the optical purity of the mixture?

A) 25%
B) 33 1/3%
C) 50%
D) 75%
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23
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
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24
What is the relationship between these two structures?
HINT: Build the molecular models and compare!
<strong>What is the relationship between these two structures? HINT: Build the molecular models and compare!  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
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25
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) identical structures B) enantiomers C) diastereomers D) constitutional isomers

A) identical structures
B) enantiomers
C) diastereomers
D) constitutional isomers
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26
What is the relationship between these two structures?
<strong>What is the relationship between these two structures?  </strong> A) Identical structures B) Enantiomers C) Diastereomers D) Constitutional isomers

A) Identical structures
B) Enantiomers
C) Diastereomers
D) Constitutional isomers
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27
The priority order for the following groups are (highest = 1),
The priority order for the following groups are (highest = 1),
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28
The priority order for the following groups is (highest = 1),
The priority order for the following groups is (highest = 1),
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29
Which statement about enantiomers is false?

A) enantiomers have the same boiling and melting points.
B) enantiomers have the same chemical properties in an achiral environment.
C) enantiomers have the same atom connectivity.
D) enantiomers have the same three dimensional orientation.
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30
Which are meso compounds?
<strong>Which are meso compounds?  </strong> A) I and II B) II and III C) I and III D) III and IV

A) I and II
B) II and III
C) I and III
D) III and IV
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31
Which are meso compounds?
<strong>Which are meso compounds?  </strong> A) I, II B) I, III C) II, III D) III, IV

A) I, II
B) I, III
C) II, III
D) III, IV
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32
How many stereoisomers are possible for Prilosec?
<strong>How many stereoisomers are possible for Prilosec?  </strong> A) 0 B) 2 C) 4 D) 8

A) 0
B) 2
C) 4
D) 8
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33
Which are meso compounds?
<strong>Which are meso compounds?  </strong> A) I and II B) II and III C) I and III D) II and IV

A) I and II
B) II and III
C) I and III
D) II and IV
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34
The structure of the S,S enantiomer of 2,3-butanediol is,
The structure of the S,S enantiomer of 2,3-butanediol is,
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35
Tuftsin (named after Tufts University) has important functions in the human immune system. It binds to stereospecific receptors at the surface of macrophages and leukocytes, stimulating their bactericidal and tumoricidal activity. All stereocenters in this molecule have S-configurations. How many stereoisomers of tuftsin exist, which do not have the correct stereochemistry for receptor-binding?
<strong>Tuftsin (named after Tufts University) has important functions in the human immune system. It binds to stereospecific receptors at the surface of macrophages and leukocytes, stimulating their bactericidal and tumoricidal activity. All stereocenters in this molecule have S-configurations. How many stereoisomers of tuftsin exist, which do not have the correct stereochemistry for receptor-binding?  </strong> A) 7 B) 15 C) 31 D) 32

A) 7
B) 15
C) 31
D) 32
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36
The following structure is the _____________ configuration.
The following structure is the _____________ configuration.
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37
How many pairs of enantiomers are possible for cholesterol?
<strong>How many pairs of enantiomers are possible for cholesterol?  </strong> A) 16 B) 32 C) 64 D) 128

A) 16
B) 32
C) 64
D) 128
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38
Which compound is a meso compound?
<strong>Which compound is a meso compound?  </strong> A) I B) II C) III D) IV

A) I
B) II
C) III
D) IV
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39
The following structure is the _____________ configuration.
The following structure is the _____________ configuration.
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40
How many pairs of enantiomers are possible for cortisone acetate?
<strong>How many pairs of enantiomers are possible for cortisone acetate?  </strong> A) 32 B) 64 C) 128 D) 256

A) 32
B) 64
C) 128
D) 256
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41
Hydrocodone, the synthetic opiate in Vicodin contains ______ stereocenters.
Hydrocodone, the synthetic opiate in Vicodin contains ______ stereocenters.
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42
The structure of the 3S,4R enantiomer of 3-bromo-4-chlorohexane is,
The structure of the 3S,4R enantiomer of 3-bromo-4-chlorohexane is,
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43
The following structure contains ………..stereocenters.
The following structure contains ………..stereocenters.
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44
The following structure contains ___________ stereocenters.
The following structure contains ___________ stereocenters.
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45
The following structures are diastereomers.
The following structures are diastereomers.
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46
2R,4R-2-bromo-4-chloropentane and 2S,4S-2-bromo-4-chloropentane are meso compounds.
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47
Enantiomers have the same physical properties (m.p., b.p., density).
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48
Glutathione is an antioxidant, which helps to protect our cells from oxidative damage. Assign R or S configurations to the stereocenters I and II
Glutathione is an antioxidant, which helps to protect our cells from oxidative damage. Assign R or S configurations to the stereocenters I and II
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49
The following structure contains??____stereocenters.
The following structure contains??____stereocenters.
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50
The following structures are enantiomers.
The following structures are enantiomers.
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51
The diastereomer of 2R,3R-dichlorobutane is achiral.
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52
The name of the following structure is 2S,3S-2,3-dibromobutane.
The name of the following structure is 2S,3S-2,3-dibromobutane.
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53
Meso compounds rotate plane polarized light the same magnitude as enantiomers, but in opposite directions.
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54
The following structure contains __________ stereocenters.
The following structure contains __________ stereocenters.
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55
The following groups are listed in decreasing order of priority.
The following groups are listed in decreasing order of priority.
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56
The following groups are listed in decreasing order of priority.
The following groups are listed in decreasing order of priority.
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57
The following structures are __________________ (what type of stereoisomer?).
The following structures are __________________ (what type of stereoisomer?).
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58
The following structures are ________________ (what type of stereoisomer).
The following structures are ________________ (what type of stereoisomer).
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59
The diastereomers 2S,4R-2-bromo-4-chloropentane and 2S,4S-2-bromo-4-chloropentane are achiral.
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