Question: 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

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.

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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