Which alkyl halide would you expect to be more reactive in an SN2 reaction with a given

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Which alkyl halide would you expect to be more reactive in an SN2 reaction with a given nucleophile? In each case, you can assume that both alkyl halides have the same stability
a. CH3CH2CH2Br or CH3CH2CH2I
b. CH3CH2CH2Cl CH3OCH2Cl
c.

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Organic Chemistry

ISBN: 978-0131407480

4th edition

Authors: Paula Yurkanis Bruice

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Question Posted: Jun 10, 2016 06:18 AM

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Which alkyl halide would you expect to be more reactive in an SN2 reaction with a given

Question:

CH3 CH2CHs CH3CH2CHBr or CH3CH2CHBr CH3 CH3 CH.CHCHCHBr rCHHCHCH,B CH CH Br or CH2CHCH3 Br Br CH2Bror CH3CH-CCH3 or CH3CH- CHCHCH3 Br Br

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a CH 3 CH 2 CH 2 I I is a weaker base than Br so 1 is ...View the full answer

Organic Chemistry

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