Among the following the most reactive alkyl halide is

.

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B) It involves the formation of a carbocation from eliminating a good leaving group.

(ii) Neopentyl chloride (CH3)3CCH2Cl does not follow SN2 mechanism.

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The order of alkyl halide reactivity in nucleophilic substitutions is the same as their order in eliminations.

This happens because as the size increases the halide ion becomes a better leaving group.

.

As alkyl groups are electron donating, they allow the positive charge in the carbocation to be delocalised by the induction effect.

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.

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Which alkyl halide out of the following may follow both SN1 and SN2 mechanism A.

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