In the following reaction, the product (A) is

Which of the following will be the most stable diazonium salt $(RN_2^+X^-)$?

The electrolytic reduction of nitrobenzene in strongly acidic medium produces

Identify A and predict the type of reaction.$$ NaNH$_2 \rightarrow A$ OCH$_3$ Br

The correct increasing order of basic strength for the following compound is:

Which of the following reactions is appropriate for converting acetamide to methanamine?

Nitration of aniline in strong acidic medium also gives m-nitroaniline because

The compound C$_7$H$_8$ undergoes the following reactions:$\newline C_7H_8 \xrightarrow{3 Cl_2 / \Delta} A \xrightarrow{Br_2/Fe} B \xrightarrow{Zn/HCl} C \newline$The compound C is

Match the following:

The major product of the following reaction is:?

The correct order of the basic strength of methyl substituted amines in aqueous solution is:

Which of the following amines will give the carbylamine test?

Identify the compound that will react with Hinsberg’s reagent to give a solid which dissolves in alkali.

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 $300K. \\$Choose the most appropriate answer from the options given below:

Which of the following reaction will NOT give primary amine as the product?

$\newline$Given below are two statements: $\newline$Statement I: Aniline does not undergo Friedel-Crafts alkylation reaction. $\newline$Statement II: Aniline cannot be prepared through Gabriel synthesis. $\newline$ $\newline$In the light of the above statements, choose the correct answer from the options given below:

Identify the major product C formed in the following reaction sequence: $\newline CH₃-CH₂-CH₂-I \xrightarrow{NaCN} A \xrightarrow[partial hydrolysis]{OH⁻} B \xrightarrow[Br₂]{NaOH} C \ (major)$