Increasing order of reactivity of the following compounds for $S_N1$ substitution is:
$(a)$ $(CH_3)_2CH-CH_2Cl$
$(b)$ $CH_3CH_2Cl$
$(c)$ $CH_3O-C_6H_4-CH_2Cl$
$(d)$ $C_6H_5-CH_2Cl$

Which among the following compounds will undergo the fastest $S_{N}2$ reaction?

Conversion of $I$ to $II$:

Compound $C_4H_8Cl_2$ $(A)$ on hydrolysis gives a compound $C_4H_8O$ $(B)$ which reacts with hydroxylamine and does not give any test with Tollen's reagent. What are $(A)$ and $(B)$?

For the following compounds,the correct statement$(s)$ with respect to nucleophilic substitution reactions is(are):
$I$: Benzyl bromide $(C_6H_5CH_2Br)$
$II$: Cyclohexylmethyl bromide $(C_6H_{11}CH_2Br)$
$III$: tert-Butyl bromide $((CH_3)_3CBr)$
$IV$: $1-$Phenylethyl bromide $(C_6H_5CH(CH_3)Br)$
$A$. $I$ and $III$ follow $S_{N}1$ mechanism
$B$. $I$ and $II$ follow $S_{N}2$ mechanism
$C$. Compound $IV$ undergoes inversion of configuration
$D$. The order of reactivity for $I$,$III$ and $IV$ is: $IV > I > III$

Which of the following halogens reacts explosively with alkanes?