Benzyl bromide reacts with H2O in formic acid solution to yield benzyl alcohol, the rate is independent of [H2O]. Under the same conditions p-methyl benzyl bromide reacts 58 times as fast.
Benzyl bromide reacts with NaOEt in EtOH to yield benzyl ethyl ether; the rate depends on both [RBr] and [OEt-].
Under the same conditions p-methyl benzyl bromide reacts 1.5 times as fast.
Account in detail for these observations.

'x' gm of a compound A3B2C5 contains 'y' gm of A atoms

 

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how to represent the possible fischer projections for 2-bromohexane