Deck 6: Sterechemistry at Tetrahedral Centers

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Question
Which of the following has a plane of symmetry?

A) boot
B) laboratory beaker
C) hammer
D) both b and c
E) none of these
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Question
Match each definition to a term from the list below.
Is an atom in a molecule that is bonded to four different atoms or groups of atoms.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
Question
Match each definition to a term from the list below.
Are designated either (±) or d,l.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
Question
Match each definition to a term from the list below.
Describes an sp3-hybridized atom that can become a chirality center by changing one of its attached groups.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
Question
Instructions: Place asterisks at all the chirality centers in each molecule below.
Place asterisks: Instructions: Place asterisks at all the chirality centers in each molecule below. Place asterisks:   codeine<div style=padding-top: 35px> codeine
Question
If (+)-sucrose has a specific rotation of +66.47, what is the specific rotation of -)-sucrose?

A) +66.47
B) -66.47
C) +33.43
D) -33.43
E) Must be determined with a polarimeter.
Question
Which of the following physical properties can be used to identify a compound?

A) R
B) S
C) ( α\alpha )
D) ([ α\alpha ]D)
Question
Instructions: Place asterisks at all the chirality centers in each molecule below.
Place asterisks: Instructions: Place asterisks at all the chirality centers in each molecule below. Place asterisks:   ephedrine<div style=padding-top: 35px> ephedrine
Question
The numbers on the carbon center of the following molecule represent atomic numbers. <strong>The numbers on the carbon center of the following molecule represent atomic numbers.   The molecule is in</strong> A) the R configuration. B) the S configuration. C) The carbon is not a chiral center in this molecule. D) The exact configuration cannot be determined without knowing additional atomic numbers. <div style=padding-top: 35px> The molecule is in

A) the R configuration.
B) the S configuration.
C) The carbon is not a chiral center in this molecule.
D) The exact configuration cannot be determined without knowing additional atomic numbers.
Question
Match each definition to a term from the list below.
Are stereoisomers that are not mirror images.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
Question
Instructions: Consider the structure of streptimidone below to answer the following question(s). Instructions: Consider the structure of streptimidone below to answer the following question(s).   streptimidone Refer to instructions. Does streptimidone have a meso stereoisomer? Explain.<div style=padding-top: 35px> streptimidone
Refer to instructions. Does streptimidone have a meso stereoisomer? Explain.
Question
Instructions: In the molecules below, assign R, S configurations to the chirality center indicated with an arrow. Instructions: In the molecules below, assign R, S configurations to the chirality center indicated with an arrow.   Refer to instructions. The configuration of the carbon atom labeled 19 is _____.<div style=padding-top: 35px>
Refer to instructions. The configuration of the carbon atom labeled 19 is _____.
Question
Instructions: Consider the structure of streptimidone below to answer the following question(s). Instructions: Consider the structure of streptimidone below to answer the following question(s).   streptimidone Refer to instructions. Assign R or S configuration to each chirality center indicated in streptimidone.<div style=padding-top: 35px> streptimidone
Refer to instructions. Assign R or S configuration to each chirality center indicated in streptimidone.
Question
Match each definition to a term from the list below.
Are molecules which contain both chirality centers and a plane of symmetry.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
Question
(-)-cholesterol

A) does not have a chiral center.
B) is dextrorotatory.
C) rotates the plane of polarized light counterclockwise.
D) does not rotate polarized light.
Question
Match each definition to a term from the list below.

Describes organic molecules which rotate plane-polarized light.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
Question
Instructions: In the molecules below, assign R, S configurations to the chirality center indicated with an arrow. Instructions: In the molecules below, assign R, S configurations to the chirality center indicated with an arrow.   Refer to instructions. The configuration of the carbon atom labeled 20 is _____.<div style=padding-top: 35px>
Refer to instructions. The configuration of the carbon atom labeled 20 is _____.
Question
Instructions: Place asterisks at all the chirality centers in each molecule below.
Rank the following substituent groups from highest to lowest priority according to the sequencing rules.
CO2CH3,CO2H,OH,Cl
Question
Instructions: Place asterisks at all the chirality centers in each molecule below.
Place asterisks: Instructions: Place asterisks at all the chirality centers in each molecule below. Place asterisks:   cephalexin<div style=padding-top: 35px> cephalexin
Question
The biological importance of enantiomers arises from?

A)Biological reactions involve receptor molecules.
B)Biological receptors are chiral.
C)Biological receptors require a specific enantiomer for reaction.
D)Each enantiomer has different biological properties.
E)all of these
Question
Which of the following structures contain a plane of symmetry? <strong>Which of the following structures contain a plane of symmetry?  </strong> A) 1 B) 2 C) 3 D) All three contain a plane of symmetry <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) All three contain a plane of symmetry
Question
What is the relationship between the following pair of structures? <strong>What is the relationship between the following pair of structures?  </strong> A) They are enantiomers B) They are diastereomers C) The are constitutional isomers D) They are identical <div style=padding-top: 35px>

A) They are enantiomers
B) They are diastereomers
C) The are constitutional isomers
D) They are identical
Question
What is the relationship between the following pair of structures? <strong>What is the relationship between the following pair of structures?  </strong> A) They are enantiomers B) They are diastereomers C) The are constitutional isomers D) They are identical <div style=padding-top: 35px>

A) They are enantiomers
B) They are diastereomers
C) The are constitutional isomers
D) They are identical
Question
Instructions:
Refer to the structure below to answer the following questions. <strong>Instructions: Refer to the structure below to answer the following questions.    -Refer to instructions. (S)-(-)-Serine:</strong> A) is dextrorotatory B) rotates plane-polarized light in a counterclockwise direction C) rotates plane-polarized light in a clockwise direction D) is racemic <div style=padding-top: 35px>

-Refer to instructions. (S)-(-)-Serine:

A) is dextrorotatory
B) rotates plane-polarized light in a counterclockwise direction
C) rotates plane-polarized light in a clockwise direction
D) is racemic
Question
How many stereoisomers of 3-bromo-2-butanol exist? <strong>How many stereoisomers of 3-bromo-2-butanol exist?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
How many stereoisomers of 2,3-dimethylbutane exist? <strong>How many stereoisomers of 2,3-dimethylbutane exist?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following correctly describes a molecule that is achiral?

A) Non-superimposability of the molecule on its mirror image
B) Superimposability of the molecule on its mirror image
C) Contains a carbon atom with four different substituents
D) Does not have a plane of symmetry
E) Both b and d
Question
Which of the following is the definition of a meso compound?

A) A molecule with chirality centers which is chiral
B) A molecule with chirality centers which is not chiral
C) A diastereomer with no chirality centers
D) A chiral compound with more than one chirality center
Question
Which of the following have the R configuration? <strong>Which of the following have the R configuration?  </strong> A) only 1 B) only 2 C) only 1 and 2 D) 1, 2 and 3 <div style=padding-top: 35px>

A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3
Question
Which of the following is the definition of a pair of diastereomers?

A) A pair of structures that are superimposable mirror images of one another
B) A pair of stereoisomers that are non-superimposable mirror images of one another
C) A pair of stereoisomers that are not mirror images of one another
D) A pair of stereoisomers that have equal specific rotations
Question
Which of the following compounds is (are) achiral? <strong>Which of the following compounds is (are) achiral?  </strong> A) only 1 B) only 1 and 2 C) only 2 and 3 D) 1, 2 and 3 <div style=padding-top: 35px>

A) only 1
B) only 1 and 2
C) only 2 and 3
D) 1, 2 and 3
Question
How many stereoisomers of 3-chloro-2-methylbutane exist? <strong>How many stereoisomers of 3-chloro-2-methylbutane exist?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following structures represent the same stereoisomer? <strong>Which of the following structures represent the same stereoisomer?  </strong> A) only 1 and 2 B) only 1 and 3 C) only 2 and 3 D) 1, 2 and 3 <div style=padding-top: 35px>

A) only 1 and 2
B) only 1 and 3
C) only 2 and 3
D) 1, 2 and 3
Question
A natural product having [ α\alpha ]D = +40.3° has been isolated and purified. This information indicates that the natural product:

A) is racemic.
B) does not rotate plane-polarized light.
C) is levorotatory.
D) is dextrorotatory.
Question
Which of the following have the S configuration? <strong>Which of the following have the S configuration?  </strong> A) only 1 B) only 2 C) only 1 and 2 D) 1, 2 and 3 <div style=padding-top: 35px>

A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3
Question
Instructions:
Refer to the structure below to answer the following questions. Instructions: Refer to the structure below to answer the following questions.    -Refer to instructions. Draw the enantiomer of (S)-(-)-serine in a wedge-dash projection.<div style=padding-top: 35px>

-Refer to instructions. Draw the enantiomer of (S)-(-)-serine in a wedge-dash projection.
Question
Which of the following statements is true regarding pairs of enantiomers?

A) They have identical melting points
B) They have identical boiling points.
C) They rotate plane-polarized light in opposite directions
D) They produce different products in reactions with chiral reagents
E) all of these
Question
Which of the following is the definition of a pair of enantiomers?

A) A pair of structures that are superimposable mirror images of one another
B) A pair of stereoisomers that are non-superimposable mirror images of one another
C) A pair of stereoisomers that are not mirror images of one another
D) A pair of stereoisomers that have equal specific rotations
Question
Instructions:
Refer to the structure below to answer the following questions. Instructions: Refer to the structure below to answer the following questions.    -Refer to instructions. Give the complete name of the enantiomer of (S)-(-)-serine.<div style=padding-top: 35px>

-Refer to instructions. Give the complete name of the enantiomer of (S)-(-)-serine.
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Deck 6: Sterechemistry at Tetrahedral Centers
1
Which of the following has a plane of symmetry?

A) boot
B) laboratory beaker
C) hammer
D) both b and c
E) none of these
both b and c
2
Match each definition to a term from the list below.
Is an atom in a molecule that is bonded to four different atoms or groups of atoms.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
chirality center
3
Match each definition to a term from the list below.
Are designated either (±) or d,l.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
racemates
4
Match each definition to a term from the list below.
Describes an sp3-hybridized atom that can become a chirality center by changing one of its attached groups.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
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5
Instructions: Place asterisks at all the chirality centers in each molecule below.
Place asterisks: Instructions: Place asterisks at all the chirality centers in each molecule below. Place asterisks:   codeine codeine
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6
If (+)-sucrose has a specific rotation of +66.47, what is the specific rotation of -)-sucrose?

A) +66.47
B) -66.47
C) +33.43
D) -33.43
E) Must be determined with a polarimeter.
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7
Which of the following physical properties can be used to identify a compound?

A) R
B) S
C) ( α\alpha )
D) ([ α\alpha ]D)
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8
Instructions: Place asterisks at all the chirality centers in each molecule below.
Place asterisks: Instructions: Place asterisks at all the chirality centers in each molecule below. Place asterisks:   ephedrine ephedrine
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9
The numbers on the carbon center of the following molecule represent atomic numbers. <strong>The numbers on the carbon center of the following molecule represent atomic numbers.   The molecule is in</strong> A) the R configuration. B) the S configuration. C) The carbon is not a chiral center in this molecule. D) The exact configuration cannot be determined without knowing additional atomic numbers. The molecule is in

A) the R configuration.
B) the S configuration.
C) The carbon is not a chiral center in this molecule.
D) The exact configuration cannot be determined without knowing additional atomic numbers.
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10
Match each definition to a term from the list below.
Are stereoisomers that are not mirror images.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
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11
Instructions: Consider the structure of streptimidone below to answer the following question(s). Instructions: Consider the structure of streptimidone below to answer the following question(s).   streptimidone Refer to instructions. Does streptimidone have a meso stereoisomer? Explain. streptimidone
Refer to instructions. Does streptimidone have a meso stereoisomer? Explain.
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12
Instructions: In the molecules below, assign R, S configurations to the chirality center indicated with an arrow. Instructions: In the molecules below, assign R, S configurations to the chirality center indicated with an arrow.   Refer to instructions. The configuration of the carbon atom labeled 19 is _____.
Refer to instructions. The configuration of the carbon atom labeled 19 is _____.
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13
Instructions: Consider the structure of streptimidone below to answer the following question(s). Instructions: Consider the structure of streptimidone below to answer the following question(s).   streptimidone Refer to instructions. Assign R or S configuration to each chirality center indicated in streptimidone. streptimidone
Refer to instructions. Assign R or S configuration to each chirality center indicated in streptimidone.
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14
Match each definition to a term from the list below.
Are molecules which contain both chirality centers and a plane of symmetry.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
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15
(-)-cholesterol

A) does not have a chiral center.
B) is dextrorotatory.
C) rotates the plane of polarized light counterclockwise.
D) does not rotate polarized light.
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16
Match each definition to a term from the list below.

Describes organic molecules which rotate plane-polarized light.

A)racemates
B)chirality center
C)chirality
D)diastereomers
E)enantiomers
F)meso compounds
G)optically active
H)prochirality center
I)optically inactive
J)achiral
K)chirality center or meso compounds
L)enantiomers or optically active
M)optically active or optically inactive
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17
Instructions: In the molecules below, assign R, S configurations to the chirality center indicated with an arrow. Instructions: In the molecules below, assign R, S configurations to the chirality center indicated with an arrow.   Refer to instructions. The configuration of the carbon atom labeled 20 is _____.
Refer to instructions. The configuration of the carbon atom labeled 20 is _____.
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18
Instructions: Place asterisks at all the chirality centers in each molecule below.
Rank the following substituent groups from highest to lowest priority according to the sequencing rules.
CO2CH3,CO2H,OH,Cl
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19
Instructions: Place asterisks at all the chirality centers in each molecule below.
Place asterisks: Instructions: Place asterisks at all the chirality centers in each molecule below. Place asterisks:   cephalexin cephalexin
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20
The biological importance of enantiomers arises from?

A)Biological reactions involve receptor molecules.
B)Biological receptors are chiral.
C)Biological receptors require a specific enantiomer for reaction.
D)Each enantiomer has different biological properties.
E)all of these
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21
Which of the following structures contain a plane of symmetry? <strong>Which of the following structures contain a plane of symmetry?  </strong> A) 1 B) 2 C) 3 D) All three contain a plane of symmetry

A) 1
B) 2
C) 3
D) All three contain a plane of symmetry
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22
What is the relationship between the following pair of structures? <strong>What is the relationship between the following pair of structures?  </strong> A) They are enantiomers B) They are diastereomers C) The are constitutional isomers D) They are identical

A) They are enantiomers
B) They are diastereomers
C) The are constitutional isomers
D) They are identical
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23
What is the relationship between the following pair of structures? <strong>What is the relationship between the following pair of structures?  </strong> A) They are enantiomers B) They are diastereomers C) The are constitutional isomers D) They are identical

A) They are enantiomers
B) They are diastereomers
C) The are constitutional isomers
D) They are identical
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24
Instructions:
Refer to the structure below to answer the following questions. <strong>Instructions: Refer to the structure below to answer the following questions.    -Refer to instructions. (S)-(-)-Serine:</strong> A) is dextrorotatory B) rotates plane-polarized light in a counterclockwise direction C) rotates plane-polarized light in a clockwise direction D) is racemic

-Refer to instructions. (S)-(-)-Serine:

A) is dextrorotatory
B) rotates plane-polarized light in a counterclockwise direction
C) rotates plane-polarized light in a clockwise direction
D) is racemic
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25
How many stereoisomers of 3-bromo-2-butanol exist? <strong>How many stereoisomers of 3-bromo-2-butanol exist?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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26
How many stereoisomers of 2,3-dimethylbutane exist? <strong>How many stereoisomers of 2,3-dimethylbutane exist?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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27
Which of the following correctly describes a molecule that is achiral?

A) Non-superimposability of the molecule on its mirror image
B) Superimposability of the molecule on its mirror image
C) Contains a carbon atom with four different substituents
D) Does not have a plane of symmetry
E) Both b and d
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28
Which of the following is the definition of a meso compound?

A) A molecule with chirality centers which is chiral
B) A molecule with chirality centers which is not chiral
C) A diastereomer with no chirality centers
D) A chiral compound with more than one chirality center
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29
Which of the following have the R configuration? <strong>Which of the following have the R configuration?  </strong> A) only 1 B) only 2 C) only 1 and 2 D) 1, 2 and 3

A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3
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30
Which of the following is the definition of a pair of diastereomers?

A) A pair of structures that are superimposable mirror images of one another
B) A pair of stereoisomers that are non-superimposable mirror images of one another
C) A pair of stereoisomers that are not mirror images of one another
D) A pair of stereoisomers that have equal specific rotations
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31
Which of the following compounds is (are) achiral? <strong>Which of the following compounds is (are) achiral?  </strong> A) only 1 B) only 1 and 2 C) only 2 and 3 D) 1, 2 and 3

A) only 1
B) only 1 and 2
C) only 2 and 3
D) 1, 2 and 3
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32
How many stereoisomers of 3-chloro-2-methylbutane exist? <strong>How many stereoisomers of 3-chloro-2-methylbutane exist?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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33
Which of the following structures represent the same stereoisomer? <strong>Which of the following structures represent the same stereoisomer?  </strong> A) only 1 and 2 B) only 1 and 3 C) only 2 and 3 D) 1, 2 and 3

A) only 1 and 2
B) only 1 and 3
C) only 2 and 3
D) 1, 2 and 3
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34
A natural product having [ α\alpha ]D = +40.3° has been isolated and purified. This information indicates that the natural product:

A) is racemic.
B) does not rotate plane-polarized light.
C) is levorotatory.
D) is dextrorotatory.
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35
Which of the following have the S configuration? <strong>Which of the following have the S configuration?  </strong> A) only 1 B) only 2 C) only 1 and 2 D) 1, 2 and 3

A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3
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36
Instructions:
Refer to the structure below to answer the following questions. Instructions: Refer to the structure below to answer the following questions.    -Refer to instructions. Draw the enantiomer of (S)-(-)-serine in a wedge-dash projection.

-Refer to instructions. Draw the enantiomer of (S)-(-)-serine in a wedge-dash projection.
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37
Which of the following statements is true regarding pairs of enantiomers?

A) They have identical melting points
B) They have identical boiling points.
C) They rotate plane-polarized light in opposite directions
D) They produce different products in reactions with chiral reagents
E) all of these
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38
Which of the following is the definition of a pair of enantiomers?

A) A pair of structures that are superimposable mirror images of one another
B) A pair of stereoisomers that are non-superimposable mirror images of one another
C) A pair of stereoisomers that are not mirror images of one another
D) A pair of stereoisomers that have equal specific rotations
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39
Instructions:
Refer to the structure below to answer the following questions. Instructions: Refer to the structure below to answer the following questions.    -Refer to instructions. Give the complete name of the enantiomer of (S)-(-)-serine.

-Refer to instructions. Give the complete name of the enantiomer of (S)-(-)-serine.
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