In the following reaction,the product $(Y)$ will be:

  • A
    $4-$chloromethylphenol-$OD$
  • B
    $1-$chloromethyl$-4-$deuteriobenzene
  • C
    $4-$bromomethyl$-1-$deuteriobenzene
  • D
    $1-$deuterio$-4-$chloromethylbenzene

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Which of the following undergoes $S_N1$ reaction at the fastest rate?

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The increasing order of densities of the following alkyl halides is:
$(I)$ $n-C_3H_7Br$
$(II)$ $n-C_3H_7Cl$
$(III)$ $n-C_3H_7I$

In the given pairs of alkyl halides,in which pair is the first compound more reactive than the second compound toward $S_N2$ reaction?

The correct statement regarding nucleophilic substitution reaction in a chiral alkyl halide is:

Which among the following is most reactive via $S_N2$ mechanism?

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