Deck 16: Aldehydes and Ketones I Nucleophilic Addition to the Carbonyl Group
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Deck 16: Aldehydes and Ketones I Nucleophilic Addition to the Carbonyl Group
1
What is the correct structure for 3-methyl-5-(2,5-dinitrophenyl)pentanal? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
II
2
What is the correct IUPAC name for the following compound? 
A) (S)-3-chloro-1-hexanone
B) (S)-1-chloro-3-hexanone
C) (R)-3-chlorocyclohexanone
D) (S)-3-chlorocyclohexanone
E) (S)-1-chloro-3-cyclohexanone

A) (S)-3-chloro-1-hexanone
B) (S)-1-chloro-3-hexanone
C) (R)-3-chlorocyclohexanone
D) (S)-3-chlorocyclohexanone
E) (S)-1-chloro-3-cyclohexanone
(S)-3-chlorocyclohexanone
3
What is the correct structure for 5,5-dimethyl-2-heptanone? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
II
4
What is the correct IUPAC name for the following compound? 
A) 5,5-Dimethyl-2-heptanone
B) 5-Ethyl-5,5-dimethyl-Methyl-2-octanone
C) 5-Ethyl-5-methyl- 2-hexanone
D) 5,5-Dimethyl-2-octanone
E) 3,3-Dimethyl-6-heptanone

A) 5,5-Dimethyl-2-heptanone
B) 5-Ethyl-5,5-dimethyl-Methyl-2-octanone
C) 5-Ethyl-5-methyl- 2-hexanone
D) 5,5-Dimethyl-2-octanone
E) 3,3-Dimethyl-6-heptanone
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5
What is the correct structure for 4-chloro-3-methylbenzaldehyde? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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6
What is the correct IUPAC name for the following compound? 
A) 2-Methyl-5-heptanone
B) 7-Methyl-4-octanone
C) 6-Isopropyl-4-octanone
D) Isobutyl propyl ketone
E) 1,1-Dimethyl-4-heptanone

A) 2-Methyl-5-heptanone
B) 7-Methyl-4-octanone
C) 6-Isopropyl-4-octanone
D) Isobutyl propyl ketone
E) 1,1-Dimethyl-4-heptanone
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7
What is the correct IUPAC name for the following compound? 
A) 1,1,2-Trimethyl-1,3-hexenone
B) 1,2-Dimethyl-1,3-hexenone
C) 2,3-Dimethyl-1,3-heptenone
D) 2,3-Dimethyl-2-hepten-4-one
E) 5,6-Dimethyl-5-hepten-4-one

A) 1,1,2-Trimethyl-1,3-hexenone
B) 1,2-Dimethyl-1,3-hexenone
C) 2,3-Dimethyl-1,3-heptenone
D) 2,3-Dimethyl-2-hepten-4-one
E) 5,6-Dimethyl-5-hepten-4-one
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8
What is the correct structure for 7-bromo-1-octyn-4-one? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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9
What is the correct structure for 3-methyl-5-(4-chlorophenyl)hexanal? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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10
A correct name for the following compound would be which of those below? 
A) 2,5-Dimethyl-6-hexanal
B) 2,5-Dimethylhexanal
C) 2-Aldehydoisohexane
D) 3,5-Dimethylheptanone
E) 1-Hydro-2,5-dimethyl-1-hexanone

A) 2,5-Dimethyl-6-hexanal
B) 2,5-Dimethylhexanal
C) 2-Aldehydoisohexane
D) 3,5-Dimethylheptanone
E) 1-Hydro-2,5-dimethyl-1-hexanone
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11
Which is the proper name for the structure shown? 
A) 2-Chloro-5-aldehydotoluene
B) 6-Chloro-3-aldehydotoluene
C) 2-Methyl-4-aldehydochlorobenzene
D) 4-Chloro-3-methylbenzaldehyde
E) 4-Methyl-5-chloro-2-benzaldehyde

A) 2-Chloro-5-aldehydotoluene
B) 6-Chloro-3-aldehydotoluene
C) 2-Methyl-4-aldehydochlorobenzene
D) 4-Chloro-3-methylbenzaldehyde
E) 4-Methyl-5-chloro-2-benzaldehyde
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12
What is the correct structure for 2,3-dimethyl-2-hepten-4-one? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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13
What is the correct IUPAC name for the following compound? 
A) 2-Methyl-2-bromobutanone
B) (S)-2-Bromo-2-methylcyclobutanone
C) (R)-2-Bromo-2-methylcyclobutanone
D) (S)-1-Bromo-1-methyl-2-cyclobutanone
E) (R)-1-Bromo-1-methyl-2-cyclobutanone

A) 2-Methyl-2-bromobutanone
B) (S)-2-Bromo-2-methylcyclobutanone
C) (R)-2-Bromo-2-methylcyclobutanone
D) (S)-1-Bromo-1-methyl-2-cyclobutanone
E) (R)-1-Bromo-1-methyl-2-cyclobutanone
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14
What is the correct IUPAC name for the following compound? 
A) 2,4-dimethyl-2-pentenone
B) 2,5-dimethylcyclopenten-3-one
C) 2,4-dimethylcyclopent-2-enone
D) 3,5-dimethylcyclopent-2-enone
E) 2-methyl-5-methylcyclopent-2-enone

A) 2,4-dimethyl-2-pentenone
B) 2,5-dimethylcyclopenten-3-one
C) 2,4-dimethylcyclopent-2-enone
D) 3,5-dimethylcyclopent-2-enone
E) 2-methyl-5-methylcyclopent-2-enone
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15
What is the correct structure for 3-phenylpropanal? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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16
What is the correct IUPAC name for the following compound? 
A) 5,5-Dimethyl-2-heptanone
B) 5-Ethyl-5,5-dimethyl-Methyl-2-octanone
C) 5,5-Dimethylcycloheptanone
D) 4,4-Dimethylcycloheptanone
E) 3,3-Dimethylcycloheptanone

A) 5,5-Dimethyl-2-heptanone
B) 5-Ethyl-5,5-dimethyl-Methyl-2-octanone
C) 5,5-Dimethylcycloheptanone
D) 4,4-Dimethylcycloheptanone
E) 3,3-Dimethylcycloheptanone
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17
What is the correct structure for 5-hydroxy-2-phenyl-3-hexanone? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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18
What is the correct structure for 7-methyl-4-octanone? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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19
What is the correct structure for 2,5-dimethylhexanal? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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20
A correct name for
is?
A) 3-Benzylpropanone
B) 3-Phenylpropanal
C) 3-Benzylpropanal
D) Nonanone
E) Nonanal

A) 3-Benzylpropanone
B) 3-Phenylpropanal
C) 3-Benzylpropanal
D) Nonanone
E) Nonanal
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21
What is the final product,Z,of the following synthesis? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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22
What is the correct structure for (S)-7-bromo-1-octyn-4-one? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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23
Which is the IUPAC name for the structure shown below? 
A) (R)-5-Bromo-2-heptanal
B) (S)-5-Bromo-2-heptanal
C) (R)-5-Bromo-2-heptanone
D) (S)-5-Bromo-2-heptanone
E) (R)-3-Bromopentyl methyl ketone

A) (R)-5-Bromo-2-heptanal
B) (S)-5-Bromo-2-heptanal
C) (R)-5-Bromo-2-heptanone
D) (S)-5-Bromo-2-heptanone
E) (R)-3-Bromopentyl methyl ketone
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24
What is the correct structure for (R)-7-bromo-1-octyn-4-one? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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25
Select the structure of the major product in the following reaction. 
A) Ethylbenzene
B) 1-Phenylethanol
C) Acetophenone
D) 2-Phenylethanal
E) Vinylbenzene

A) Ethylbenzene
B) 1-Phenylethanol
C) Acetophenone
D) 2-Phenylethanal
E) Vinylbenzene
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26
Which of the compounds listed below would you expect to have the highest boiling point? (They all have approximately the same molecular weight. )
A) Pentane
B) 1-Butanol
C) Butanal
D) 1-Fluorobutane
E) Diethylether
A) Pentane
B) 1-Butanol
C) Butanal
D) 1-Fluorobutane
E) Diethylether
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27
What is the correct structure for (R)-5-bromo-2-heptanone? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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28
What is the correct structure for (S)-5-bromo-2-heptanone? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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29
Which is the IUPAC name for the structure shown below? 
A) 5-Cyclohexyl-2-hexanal
B) 5-Cyclohexyl-2-hexanone
C) 5-Cyclohexyl-5-methyl-2-pentanone
D) 5-(1-Methylcyclohexyl)-2-pentanone
E) 4-(1-Methylcyclohexyl)-2-butanone

A) 5-Cyclohexyl-2-hexanal
B) 5-Cyclohexyl-2-hexanone
C) 5-Cyclohexyl-5-methyl-2-pentanone
D) 5-(1-Methylcyclohexyl)-2-pentanone
E) 4-(1-Methylcyclohexyl)-2-butanone
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30
Which is the proper name for the structure shown below? 
A) 7-Bromo-1,4-octynal
B) 7-Bromo-1,4-octynone
C) 2-Bromo-5,7-octynal
D) 7-Bromo-7-methyl-1-heptyne-3-ketone
E) 7-Bromo-1-octyn-4-one

A) 7-Bromo-1,4-octynal
B) 7-Bromo-1,4-octynone
C) 2-Bromo-5,7-octynal
D) 7-Bromo-7-methyl-1-heptyne-3-ketone
E) 7-Bromo-1-octyn-4-one
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31
What is the correct structure for (S)-4-cyclohexyl-3-methyl-2-butanone? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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32
Select the structure of the major product in the following reaction.

A) I
B) II
C) III
D) IV
E) V


A) I
B) II
C) III
D) IV
E) V
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33
Which of the following procedures would not yield 3-pentanone as a major product?
A)

B)

C)

D)

E)

A)

B)

C)

D)

E)

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34
Which is the proper name for the structure shown? 
A) 3,5-Dimethyl-5-(4-chlorobenzyl)-1-pentanal
B) 3-Methyl-5-(4-chlorophenyl)hexanol
C) 3,5-Dimethyl-5-(4-chlorophenyl)-1-pentanaldehyde
D) 3-Methyl-5-(4-chlorophenyl)-hexanaldehyde
E) 3-Methyl-5-(4-chlorophenyl)hexanal

A) 3,5-Dimethyl-5-(4-chlorobenzyl)-1-pentanal
B) 3-Methyl-5-(4-chlorophenyl)hexanol
C) 3,5-Dimethyl-5-(4-chlorophenyl)-1-pentanaldehyde
D) 3-Methyl-5-(4-chlorophenyl)-hexanaldehyde
E) 3-Methyl-5-(4-chlorophenyl)hexanal
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35
What is the IUPAC name for
?
A) 4-Oxo-5-phenyl-2-hexanol
B) 5-Hydroxy-2-phenyl-3-hexanone
C) 2-Hydroxy-5-phenyl-4-hexanone
D) 2-Hydroxypropyl-1-phenylethyl ketone
E) 5-Hydroxy-3-keto-2-phenylhexane

A) 4-Oxo-5-phenyl-2-hexanol
B) 5-Hydroxy-2-phenyl-3-hexanone
C) 2-Hydroxy-5-phenyl-4-hexanone
D) 2-Hydroxypropyl-1-phenylethyl ketone
E) 5-Hydroxy-3-keto-2-phenylhexane
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36
What is the correct structure for (S)-4-cyclohexyl-3-methyl-2-butanone? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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37
Which is the IUPAC name for the structure shown below? 
A) (R)-5-Bromo-2-heptanal
B) (S)-5-Bromo-2-heptanal
C) (R)-5-Bromo-2-heptanone
D) (S)-5-Bromo-2-heptanone
E) (R)-3-Bromopentyl methyl ketone

A) (R)-5-Bromo-2-heptanal
B) (S)-5-Bromo-2-heptanal
C) (R)-5-Bromo-2-heptanone
D) (S)-5-Bromo-2-heptanone
E) (R)-3-Bromopentyl methyl ketone
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38
Identify the reagent(s)that would bring about the following reaction: CH3CH2CH2COCl -- CH3CH2CH2CHO
A) H2/Ni
B) Li/liq.NH3
C) LiAlH[OC(CH3)3]3,ether
D) NaBH4,CH3OH
E) LiAlH4,ether
A) H2/Ni
B) Li/liq.NH3
C) LiAlH[OC(CH3)3]3,ether
D) NaBH4,CH3OH
E) LiAlH4,ether
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39
LiAlH4 (LAH)cannot be used to convert carboxylic acids to the corresponding aldehydes because:
A) LAH is not sufficiently reactive.
B) RCOOH is converted into RCOOLi.
C) RCOOH is reduced to RCH2OH.
D) RCOOH is reduced to RCH3.
E) RCOOH is converted into R2C=O.
A) LAH is not sufficiently reactive.
B) RCOOH is converted into RCOOLi.
C) RCOOH is reduced to RCH2OH.
D) RCOOH is reduced to RCH3.
E) RCOOH is converted into R2C=O.
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40
What is the correct structure for 4-(1-methylcyclohexyl)-2-butanone? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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41
Select the structure of the major product in the following reaction. 
A) 4-Methylhexanal
B) 4-Methyl-1-hexanol
C) 3-Methylhexanal
D) 4,10-Dimethyldodecane-6,7-dione
E) 4,10-Dimethyldodecane-6,7-diol

A) 4-Methylhexanal
B) 4-Methyl-1-hexanol
C) 3-Methylhexanal
D) 4,10-Dimethyldodecane-6,7-dione
E) 4,10-Dimethyldodecane-6,7-diol
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42
Select the structure of the major product in the following reaction. 
A) 4-Methylhexanal
B) 4-Methyl-1-hexanol
C) 3-Methylhexanal
D) 4,10-Dimethyldodecane-6,7-dione
E) 4,10-Dimethyldodecane-6,7-diol

A) 4-Methylhexanal
B) 4-Methyl-1-hexanol
C) 3-Methylhexanal
D) 4,10-Dimethyldodecane-6,7-dione
E) 4,10-Dimethyldodecane-6,7-diol
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43
Select the structure of the major product in the following reaction. 
A) 3-Methylhexanal
B) 4-Methyl-1-hexanol
C) 4-Methylhexanal
D) 4,10-Dimethyldodecane-6,7-dione
E) 4,10-Dimethyldodecane-6,7-diol

A) 3-Methylhexanal
B) 4-Methyl-1-hexanol
C) 4-Methylhexanal
D) 4,10-Dimethyldodecane-6,7-dione
E) 4,10-Dimethyldodecane-6,7-diol
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44
A good synthesis of

A) I
B) II
C) III
D) IV
E) All of these are equally useful.


A) I
B) II
C) III
D) IV
E) All of these are equally useful.
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45
A good synthesis of

A) I
B) II
C) III
D) IV
E) All of these are equally useful.


A) I
B) II
C) III
D) IV
E) All of these are equally useful.
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46
Select the structure of the major product in the following reaction.

A) I
B) II
C) III
D) IV
E) V


A) I
B) II
C) III
D) IV
E) V
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47
Select the structure of the major product in the following reaction. 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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48
A good synthesis of

A) I
B) II
C) III
D) IV
E) All of these are equally useful.


A) I
B) II
C) III
D) IV
E) All of these are equally useful.
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49
A good synthesis of

A) I
B) II
C) III
D) IV
E) All of these are equally useful.


A) I
B) II
C) III
D) IV
E) All of these are equally useful.
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50
Select the structure of the major product in the following reaction. 
A) 4-Methylhexanal
B) 4-Methyl-1-hexanol
C) 3-Methylhexanal
D) 4,10-Dimethyldodecane-6,7-dione
E) 4,10-Dimethyldodecane-6,7-diol

A) 4-Methylhexanal
B) 4-Methyl-1-hexanol
C) 3-Methylhexanal
D) 4,10-Dimethyldodecane-6,7-dione
E) 4,10-Dimethyldodecane-6,7-diol
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51
Select the structure of the major product in the following reaction.

A) I
B) II
C) III
D) IV
E) V


A) I
B) II
C) III
D) IV
E) V
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52
Which synthesis or syntheses would yield propanal?
A)

B)

C)

D) All of these
E) None of these
A)

B)

C)

D) All of these
E) None of these
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53
Which of the following would yield 3-pentanone as the major product?
A)

B)

C)

D) Two of these
E) All of these
A)

B)

C)

D) Two of these
E) All of these
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54
A good synthesis of

A) I
B) II
C) III
D) IV
E) All of these are equally useful.


A) I
B) II
C) III
D) IV
E) All of these are equally useful.
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55
What would be the product of the following reaction sequence? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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56
A good synthesis of 
A) I
B) II
C) III
D) IV
E) All of these are equally useful.

A) I
B) II
C) III
D) IV
E) All of these are equally useful.
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57
Which of the following is a synthesis of 3-heptanone?
A)

B)

C)

D)

E) All of the above are syntheses of 3-heptanone.
A)

B)

C)

D)

E) All of the above are syntheses of 3-heptanone.
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58
Select the structure of the major product in the following reaction. 
A) cyclopentanol
B) 1-cyclopentylcyclopentane
C) cyclopentanone
D) cyclopentene
E) 1-(1-hydroxycyclopentyl)-1-hydroxycyclopentane

A) cyclopentanol
B) 1-cyclopentylcyclopentane
C) cyclopentanone
D) cyclopentene
E) 1-(1-hydroxycyclopentyl)-1-hydroxycyclopentane
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59
Select the structure of the major product in the following reaction. 
A) Ethylbenzene
B) 1-Phenylethanol
C) Acetophenone
D) 2-Phenylethanal
E) Vinylbenzene

A) Ethylbenzene
B) 1-Phenylethanol
C) Acetophenone
D) 2-Phenylethanal
E) Vinylbenzene
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60
Which of the following is not a synthesis of benzophenone, 
A)

B)

C)

D)

E) All of the above will give benzophenone.

A)

B)

C)

D)

E) All of the above will give benzophenone.
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61
Which compound is an acetal? 
A) I
B) II
C) III
D) IV
E) All of the above

A) I
B) II
C) III
D) IV
E) All of the above
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62
The product,D,of the following sequence of reactions
would be: 
A) I
B) II
C) III
D) IV
E) V


A) I
B) II
C) III
D) IV
E) V
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63
The product,E,of the following reaction sequence,
would be: 
A) I
B) II
C) III
D) IV
E) V


A) I
B) II
C) III
D) IV
E) V
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64
The product,K,of the following sequence of reactions
would be: 
A) I
B) II
C) III
D) IV
E) V


A) I
B) II
C) III
D) IV
E) V
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65
What,in general,is the order of increasing reactivity of these carbonyl compounds towards nucleophilic reagents? 
A) I < III < V < II < IV
B) IV < II < I < III < V
C) V< III < I < II < IV
D) II< I < V < III < IV
E) III < V < IV < II < I

A) I < III < V < II < IV
B) IV < II < I < III < V
C) V< III < I < II < IV
D) II< I < V < III < IV
E) III < V < IV < II < I
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66
The product,K,of the following sequence of reactions would be: 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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67
Which compound is a hemiacetal? 
A) I
B) II
C) III
D) IV
E) All of the above

A) I
B) II
C) III
D) IV
E) All of the above
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68
What is the final product of this synthetic sequence? 
A)

B) p-BrC6H4CH2C6H5
C) C6H5CH2COOH
D)

E) C6H5CH2C6H5

A)

B) p-BrC6H4CH2C6H5
C) C6H5CH2COOH
D)

E) C6H5CH2C6H5
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69
What would be the product of the following reaction sequence? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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70
What would be the product of the following reaction sequence? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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71
Which of these will not catalyze the reaction of a weak nucleophile with the carbonyl group of an aldehyde or ketone?
A) I-
B) H3O+
C) AlCl3
D) BF3
E) ZnCl2
A) I-
B) H3O+
C) AlCl3
D) BF3
E) ZnCl2
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72
Which of the following compounds is an acetal? 
A) I
B) II
C) III
D) IV
E) None of these

A) I
B) II
C) III
D) IV
E) None of these
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73
What new compound will eventually be formed when HCl is added to a solution of pentanal in methanol?
A)

B)

C)

D)

E)

A)

B)

C)

D)

E)

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74
The product,E,of the following reaction sequence,
would be: 
A) I
B) II
C) III
D) IV
E) V


A) I
B) II
C) III
D) IV
E) V
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75
What would be the product of the following reaction sequence? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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76
What would be the product of the following reaction sequence? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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77
Acetals are unstable in the presence of an aqueous solution of which of these?
A) HCl
B) NaOH
C) KHCO3
D) Na2CO3
E) NaCl
A) HCl
B) NaOH
C) KHCO3
D) Na2CO3
E) NaCl
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78
What would be the product of the following reaction sequence? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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79
Which is the general formula for a thioacetal?
A)

B)

C)

D)

E)

A)

B)

C)

D)

E)

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80
What,in general,is the order of decreasing reactivity of these carbonyl compounds towards nucleophilic reagents? 
A) I > III > IV > II > V
B) IV > II > I > III > V
C) V > III > I > II > IV
D) I > IV > II > III > V
E) III > V > IV > II > I

A) I > III > IV > II > V
B) IV > II > I > III > V
C) V > III > I > II > IV
D) I > IV > II > III > V
E) III > V > IV > II > I
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