Phenyl isocyanides are prepared from which of the following reactions?

Identify the correct statements:
$(A)$ Primary amines do not give diazonium salts when treated with $NaNO_2$ in acidic conditions.
$(B)$ Aliphatic and aromatic primary amines on heating with $CHCl_3$ and ethanolic $KOH$ form carbylamines.
$(C)$ Secondary and tertiary amines also give the carbylamine test.
$(D)$ Benzenesulfonyl chloride is known as Hinsberg's reagent.
$(E)$ Tertiary amines react with benzenesulfonyl chloride very easily.
Choose the correct answer from the options given below:

Given below are two statements: one is labelled as Assertion $(A)$ and the other is labelled as Reason $(R)$.
Assertion $(A)$: Experimental reaction of $CH_{3}Cl$ with aniline and anhydrous $AlCl_{3}$ does not give $o-$ and $p-$methylaniline.
Reason $(R)$: The $-NH_{2}$ group of aniline becomes deactivating because of salt formation with anhydrous $AlCl_{3}$ and hence yields $m-$methylaniline as the product.
In the light of the above statements,choose the most appropriate answer from the options given below.

In the following reaction,the reason why the meta-nitro product is also formed is:

In the following reaction,$X$ is:
$X$ $\xrightarrow{\text{Bromination}} Y$ $\xrightarrow{NaNO_2 + HCl} Z$ $\xrightarrow[C_2H_5OH]{\text{Boiling}} \text{1,3,5-Tribromobenzene}$

Product of the reaction is