Deck 6: Sterechemistry at Tetrahedral Centers
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ملء الشاشة (f)
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
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
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
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
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:
codeine
Place asterisks:
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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.
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) ( )
D) ([ ]D)
A) R
B) S
C) ( )
D) ([ ]D)
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8
Instructions: Place asterisks at all the chirality centers in each molecule below.
Place asterisks:
ephedrine
Place asterisks:
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9
The numbers on the carbon center of the following molecule represent 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.
The molecule is inA) 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
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).
streptimidone
Refer to instructions. Does streptimidone have a meso stereoisomer? Explain.
streptimidoneRefer 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. 
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).
streptimidone
Refer to instructions. Assign R or S configuration to each chirality center indicated in streptimidone.
streptimidoneRefer 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
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.
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
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. 
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
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:
cephalexin
Place asterisks:
cephalexin فتح الحزمة
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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
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? 
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? 
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? 
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.
-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
Refer to the structure below to answer the following questions.

-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? 
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? 
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
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
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? 
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
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? 
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? 
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? 
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 [ ]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.
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? 
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.
-Refer to instructions. Draw the enantiomer of (S)-(-)-serine in a wedge-dash projection.
Refer to the structure below to answer the following questions.

-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
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
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.
-Refer to instructions. Give the complete name of the enantiomer of (S)-(-)-serine.
Refer to the structure below to answer the following questions.

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