$(a)$ $\begin{array}{*{20}{c}}
{\,\,\,\,\,\begin{array}{*{20}{c}}
{\,I} \\
|
\end{array}} \\
{C{H_3} - C - H} \\
{\,\,\,\,|} \\
{\,\,\,\,\,\,\,\,\,\,C{H_3}}
\end{array}$ , Isopropyl iodide $(2^o)$
$(b)$ $\begin{array}{*{20}{c}}
{\begin{array}{*{20}{c}}
{\,\,\,\,H\,\,\,\,\,\,H\,\,\,\,\,H} \\
{\,\,\,|\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,|}
\end{array}} \\
{H - C - C - C - I} \\
{\,\,\,\,|\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,|\,} \\
{\,\,\,\,\,\,\,\,\,\,H\,\,\,\,\,\,H\,\,\,\,\,C{H_3}}
\end{array}$, sec- Butyl iodide $(2^o)$
$(c)$ $\begin{array}{*{20}{c}}
{\,\,\,\,\,\,\,\,\begin{array}{*{20}{c}}
{\,\,\,\,\,\,C{H_3}} \\
|
\end{array}\,} \\
{{H_3}C - C - I} \\
{\,\,\,\,\,|} \\
{\,\,\,\,\,\,\,\,\,\,C{H_3}}
\end{array}$ , tert - Butyl iodide $(3^o)$
$(d)$ $\begin{array}{*{20}{c}}
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\begin{array}{*{20}{c}}
{\,\,\,C{H_3}\,\,H\,\,} \\
{|\,\,\,\,\,\,\,\,\,|}
\end{array}} \\
{C{H_3} - C{H_2} - C - C - Cl} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,|\,} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,CH{\,_3}\,H\,\,\,\,\,\,}
\end{array}$, Neohexyl chloride $(1^o)$
Thus, $(d)$ is a primary $(1^o)$ halide.
${\left( {C{H_3}} \right)_2}CH - OH\xrightarrow{{PB{r_3}}}X\xrightarrow{{alko.\,\,KOH}}Y\xrightarrow[{(ii)\,{H_3}{O^ + }}]{{(i)\,{H_2}S{O_4}}}Z$

$\left. \begin{gathered}
(A)\,\,\xrightarrow{{PB{r_3}}}\,(C)\,\xrightarrow{{Mg\,,\,ether}}Grignard\,\,reagent \hfill \\
(A)\,\,\xrightarrow[{{H_2}S{O_4}}]{{N{a_2}C{r_2}{O_7}}}\,(B) \hfill \\
\end{gathered} \right\}$ $ \to \,(D)\xrightarrow{{{H_3}{O^ \oplus }}}$ $(3,4-$ ડાયમિથાઇલ $3-$ હેકઝાનોલ l$)$

