$(i)$ $\begin{array}{*{20}{c}}
{\begin{array}{*{20}{c}}
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{H_3}-CH_2} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,|}
\end{array}} \\
{C{H_3} - {C^ + }} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,|} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{H_3}}
\end{array}$
$(ii)$ $\begin{array}{*{20}{c}}
{\begin{array}{*{20}{c}}
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{H_3}} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,|}
\end{array}} \\
{C{H_3} - {C^ + }} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,|} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,{H}}
\end{array}$
$(iii)$ $\begin{array}{*{20}{c}}
{\begin{array}{*{20}{c}}
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{H_3}} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,|}
\end{array}} \\
{C{H_3} - {C^ + }} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,|} \\
{\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{H_3}}
\end{array}$
$(iv)$ $Ph - CH ^{+}-\underline{ CH }_{3}$
Carbocation \((i)\) shows eight hyperconjugation structures.
Carbocation \((ii)\) shows six hyperconjugation structures.
Carbocation \((iii)\) shows nine hyperconjugation structures.
Carbocation \((iv)\) shows \(+M\) effect.
Therefore, the correct stability order is : \(iv > iii > i > ii\)
$(A) \,\,CH_3-CH_2-NH_2$