A) It is fastest with tertiary halides.
B) All bonds are broken and formed in a single step.
C) It exhibits first-order kinetics.
D) A better leaving group should make a faster reaction.
F) B) and D)
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C
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A) II
B) III
C) IV
D) I
F) A) and B)
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A) I = Monosubstituted; II = disubstituted; III = trisubstituted
B) I = Disubstituted; II = disubstituted; III = trisubstituted
C) I = Disubstituted; II = trisubstituted; III = disubstituted
D) I = Disubstituted; II = trisubstituted; III = trisubstituted
F) All of the above
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D
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A) Rate =k[CH3CH2CH2Br][KOC(CH3) 3]
B) Rate =k[CH3CH2CH2Br]2[KOC(CH3) 3]
C) Rate =k[CH3CH2CH2Br]
D) Rate = k[CH3CH2CH2Br][KOC(CH3) 3]2
F) B) and C)
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A) III
B) II
C) I
D) IV
F) All of the above
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A) The reaction is slowest with tertiary substrates.
B) The reaction follows second-order kinetics.
C) The identity of the leaving group affects the rate of reaction.
D) Polar aprotic solvents favor the E1 mechanism.
F) A) and B)
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C
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A) III
B) II
C) IV
D) I
F) A) and D)
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A) The reaction follows first-order kinetics.
B) Stronger bases favor the E1 reaction.
C) The reaction is fastest with tertiary alkyl halides.
D) A better leaving group makes the reaction rate increase.
F) B) and C)
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A) I
B) IV
C) III
D) II
F) B) and C)
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