A) [1] LiAlH4, [2] H2O
B) [1] CH2=CHLi, [2] H2O
C) [1] (CH2=CH) 2CuLi, [2] H2O
D) [1] DIBAL-H, [2] H2O
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) NaBH4
B) LiAlH(OtBu) 3
C) LiAlH4
D) FeCl3
Correct Answer
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Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
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Multiple Choice
A) The bond angle of the carbonyl is larger than the bond angle of the alkene.
B) The electronegative oxygen of the C=O group makes this bond polar.
C) The bond of the C=C is longer that the bond of the C=O.
D) There is more steric crowding in the carbonyl than in the alkene.
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) PhMgBr then H2O
B) Benzene, AlCl3
C) Ph2CuLi then H2O
D) PhLi then H2O
Correct Answer
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Multiple Choice
A) Both reagents contain polar metal-hydrogen bonds.The polarity of the B-H bond is greater than the polarity of the Al-H bond, so LiAlH4 is the stronger reducing agent.
B) Both reagents contain polar metal-hydrogen bonds.The polarity of the B-H bond is greater than the polarity of the Al-H bond, so LiAlH4 is the weaker reducing agent.
C) Both reagents contain polar metal-hydrogen bonds.The polarity of the B-H bond is less than the polarity of the Al-H bond, so LiAlH4 is the stronger reducing agent.
D) Both reagents contain polar metal-hydrogen bonds.The polarity of the B-H bond is less than the polarity of the Al-H bond, so LiAlH4 is the weaker reducing agent.
Correct Answer
verified
Multiple Choice
A) [1] LiAlH4, [2] H2O
B) [1] CH3MgBr (excess) , [2] H2O
C) [1] (CH3) 2CuLi (excess) , [2] H2O
D) [1] DIBAL-H, [2] H2O
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
Multiple Choice
A) NaBH4
B) LiAlH4
C) H2 and Pd-C
D) DIBAL-H
Correct Answer
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Multiple Choice
A) Electrophilic addition
B) Nucleophilic addition
C) Nucleophilic substitution
D) Electrophilic substitution
Correct Answer
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Multiple Choice
A) Bromobenzene
B) Benzyl bromide
C) Benzoic acid
D) Lithium benzoate
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
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Multiple Choice
A) Ketones are more sterically hindered.
B) Ketones are less electron deficient due to donation from the two alkyl groups.
C) The statement is false; ketones are more reactive than aldehydes.
D) Both (a) Ketones are more sterically hindered and (b) Ketones are less electron deficient due to donation from the two alkyl groups.
Correct Answer
verified
Multiple Choice
A) If it isn't protected, the product will be a carboxylic acid.
B) The Grignard reagent will react with the alcohol before the ketone.
C) Magnesium is Lewis acidic and will coordinate with the alcohol.
D) There is no need to protect the alcohol.
Correct Answer
verified
Multiple Choice
A) I
B) II
C) III
D) IV
Correct Answer
verified
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