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Multiple Choice
A) 2,2-dimethyl-1-butanol
B) 3,3-dimethyl-2-butanol
C) 3,3-dimethyl-1-butanol
D) 2,3-dimethyl-2-butanol
E) 2,3-dimethyl-1-butanol
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Multiple Choice
A) SN2 and SN1
B) E1 and E2
C) SN2 and E2
D) E1 and SN1
E) E2 and SN1
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Multiple Choice
A) reaction products when CH3I is used as the substrate
B) reaction products when (CH3) 3CCH2I is used as substrate
C) the stereochemistry of nucleophilic substitutions
D) the effect of nucleophile concentration on rate
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Multiple Choice
A)
B)
C)
D)
E) none of the above
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Multiple Choice
A)
B) CH3CH2CH CH2
C)
D)
E)
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Multiple Choice
A) no change
B) doubles the rate
C) triples the rate
D) quadruples the rate
E) rate is halved
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Multiple Choice
A) (CH3) 3CCH2I
B) (CH3) 3CCl
C) (CH3) 2CHI
D) (CH3) 2CHCH2CH2CH2Cl
E) (CH3) 2CHCH2CH2CH2I
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Multiple Choice
A) the nature of the alkyl halide
B) the nature of the leaving group
C) the concentration of the alkyl halide
D) the concentration of the nucleophile
E) the value of the rate constant
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Multiple Choice
A) no change
B) doubles the rate
C) triples the rate
D) quadruples the rate
E) rate is halved
Correct Answer
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