Which alkyl halide would you expect to be more reactive in an S2 reaction with a...

 

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Which alkyl halide would you expect to be more reactive in an S2 reaction with a given nucleophile? In each case, you can assume that both alkyl halides have the same stability. a. CH₂CH₂CH₂Br or CH₂CH₂CH₂1 b. CH3CH₂CH₂Cl or CH₂OCH₂Cl CH₁ CH₂CH3 c. CH₂CH₂CHBr or CH₂CH₂CHBr CH3 CH3 d. CH₂CH₂CH₂CHBr or CH₂CH₂CHCH,Br e. -CH₂CH₂Br or f. -CH₂Br or g. CH₂CH=CCH3 or CH₂CH=CHCHCH₂ Br For each of the pairs reaction? -CH₂CHCH₂ Br -Br Br , which compound would be more reactive in an Sl Show the configuration of the products obtained from the following reaction: a. under conditions that favor an SN2 reaction b. under conditions that favor an Syl reaction CH₂CH=CHCH₂Br + CH₂O™ CH₂OH Which alkyl halide would you expect to be more reactive in an S2 reaction with a given nucleophile? In each case, you can assume that both alkyl halides have the same stability. a. CH₂CH₂CH₂Br or CH₂CH₂CH₂1 b. CH3CH₂CH₂Cl or CH₂OCH₂Cl CH₁ CH₂CH3 c. CH₂CH₂CHBr or CH₂CH₂CHBr CH3 CH3 d. CH₂CH₂CH₂CHBr or CH₂CH₂CHCH,Br e. -CH₂CH₂Br or f. -CH₂Br or g. CH₂CH=CCH3 or CH₂CH=CHCHCH₂ Br For each of the pairs reaction? -CH₂CHCH₂ Br -Br Br , which compound would be more reactive in an Sl Show the configuration of the products obtained from the following reaction: a. under conditions that favor an SN2 reaction b. under conditions that favor an Syl reaction CH₂CH=CHCH₂Br + CH₂O™ CH₂OH