Given below are two statements: Statement I: Primary aliphatic amines react with $HNO_2$ to give unstable diazonium salts. Statement II: Primary aromatic amines react with $HNO_2$ to form diazonium salts which are stable even above $300\text{ K}$. In the light of the above statements, choose the most appropriate answer from the options given below:

The products formed when Aniline reacts with $Br_2$ water, and $NaNO_2/HCl$ will be, respectively:

Aniline gives a set of the following reactions that yielded a coloured product 'Y'. The structure of 'Y' is: (Note: Reaction scheme is missing from the provided text)

The structure of C in the below-mentioned reaction is: (Note: Reaction scheme is missing from the provided text)

What results from the electrolytic reduction of nitrobenzene in a highly acidic medium?

The reagent required to convert acetamide into methyl amine is:

D is N-methyl aniline in the given below sequence of reaction: $A \xrightarrow{\text{reduction}} B \xrightarrow{CHCl_3/KOH} C \xrightarrow{\text{reduction}} D$. Structure of A can be:

Which of the following statements about primary amines is false?

What is the correct order of the methyl-substituted amines' basic strength in an aqueous solution?