\(Cl_2/ AlCl_3 \Rightarrow\) Electrophilc aromatic substitution.
According to Baker-Nathan effect, hyperconjugation dominates over inductive effect. Hence ortho-position of methyl group has more \(e^-\) density for \(EAS\)
$X\xrightarrow[\Delta ]{{{H}_{2}}O}A+B+C+D$
$CH_3CH(Cl)CH_2 - CH_2OH \xrightarrow{Aq.KOH}$ is
${C_2}{H_5}I\xrightarrow{{Alco.\,\,KOH}}X\xrightarrow{{B{r_2}}}Y\xrightarrow{{KCN}}Z$
$(a)$ $\begin{array}{*{20}{c}}
{C{H_3} - CH - Br} \\
{|\,} \\
{\,\,\,\,\,\,{C_2}{H_5}}
\end{array}$
$(b)$ $\begin{array}{*{20}{c}}
{\begin{array}{*{20}{c}}
{\,\,Br} \\
|
\end{array}} \\
{C{H_3} - C - C{H_3}} \\
| \\
{\,\,\,\,\,\,\,\,\,{C_2}{H_5}}
\end{array}$
$(c)$ $\begin{array}{*{20}{c}}
{C{H_3}{\mkern 1mu} - CH{\mkern 1mu} - {\mkern 1mu} {\mkern 1mu} C{H_2}Br} \\
{|\,\,\,\,\,\,\,\,\,\,\,\,\,} \\
{{C_2}{H_5}\,\,\,}
\end{array}$