A)
B)
C)
D)
E)
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Multiple Choice
A)
B)
C)
D)
E)
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Essay
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View Answer
Multiple Choice
A) NH3; Cl2/AlCl3
B) Cl2/AlCl3; NH3
C) Cl2/AlCl3; HNO3/H2SO4; Sn/HCl, HO-
D) HNO3/H2SO4; Cl2/AlCl3; Sn/HCl, HO-
E) HNO3/H2SO4; Sn/HCl; HO-; Cl2/AlCl3
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Multiple Choice
A) HSO3+
B) SO2+
C) HSO3-
D) H2SO4
E) HSO4-
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Essay
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Short Answer
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Multiple Choice
A) HNO3
B) NO3
C) NO
D) NO2
E) NO2+
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Essay
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Multiple Choice
A) An alkyl group substitutes for a hydrogen.
B) The benzene ring attacks an acylium ion.
C) The acylium ion is resonance stabilized.
D) The acylium ion is often produced from an acyl chloride.
E) More than one equivalent of Lewis acid must be used.
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Multiple Choice
A) I
B) II
C) III
D) IV
E) V
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Multiple Choice
A) I
B) II
C) III
D) IV
E) V
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Essay
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Multiple Choice
A) It serves as a radical initiator to produce the chlorine radical needed to propagate the chain reaction.
B) It functions by destabilizing the carbocationic intermediate and thereby increases the rate of H+ loss.
C) It serves as a Lewis base catalyst by reacting with Cl2 to generate chloride ions.
D) It functions by destabilizing the benzene through formation of a π-complex.
E) It serves as a Lewis acid catalyst by reacting with the Cl2 and thereby activates it toward attack by benzene's π electrons.
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Multiple Choice
A)
B)
C)
D)
E)
Correct Answer
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Multiple Choice
A)
B)
C)
D)
E)
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Essay
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Essay
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Multiple Choice
A) -Br
B)
C) -OCH3
D)
E) -CCl3
Correct Answer
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Essay
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