The reaction of amides with $Br_2$ and $OH^-$ (Hofmann bromamide degradation) involves an intramolecular migration of the alkyl group from the carbonyl carbon to the nitrogen atom with retention of configuration at the migrating center. Predict the products for the following reaction:
(Image shows two substituted cyclohexanecarboxamides reacting with $Br_2/OH^-$)

What is the major product obtained from the following reaction?

Which of the following can form intermolecular $H$-bond?

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:

Identify $Z$ in the following sequence of reactions.

Among the following compounds nitrobenzene,benzene,aniline and phenol,the strongest basic behaviour in acid medium is exhibited by