Which of the following reactions will not give a primary amine?

Given below are two statements:
Statement-$I$ : Oxidation of $p$-nitrotoluene with acidic $KMnO_4$ gives an acid that is stronger than benzoic acid.
Statement-$II$ : Reduction of $p$-nitrotoluene with $Sn/HCl$ followed by neutralization gives an amine that is more basic than aniline.
In light of the above statements, choose the most appropriate answer from the options given below.

The product $(A)$ is:

$E \xleftarrow{KOH/Br_2} D \xleftarrow{H_2O_2/OH^{-} \atop (Partial \ Hydrolysis)} C \xleftarrow{NaCN} C_2H_5-Cl$ $\xrightarrow{AgCN} A$ $\xrightarrow{LiAlH_4} B$
What is the relationship between $B$ and $E$?

Benzyl isocyanide can be obtained from which of the following reactions? Choose the correct answer from the options given below:
$A$. Benzyl bromide + $AgCN$
$B$. Benzylamine + $CHCl_3$ + $Aq. NaOH$
$C$. Bromobenzene + $AgCN$
$D$. Aniline + $CHCl_3$ + $Aq. NaOH$
$E$. $2-$Phenylethyl bromide + $KCN$

$(a) \, CH_3CONH_2 + KOH + Br_2 \rightarrow$
$(b) \, CH_3COOH + \text{Soda lime} \rightarrow$
$(c) \, CH_3COOAg + Br_2 \rightarrow$
What is the common feature in the above three reactions?