The given reaction sequence is;
Step 1: Diazotization. The first step involves the reaction of the given compound (2-hydroxycyclohexanone) with sodium nitrite (NaNO2) and hydrochloric acid (HCl). This is a diazotization reaction, which converts the amino group (-NH2) of an aromatic amine to a diazonium salt (-N+ 2Cl−). This reaction doesn’t happen with the carbonyl group. Since the starting compound shown is not an amino compound, it needs to have NH2 for diazotization reaction to happen. Hence it would be more logical if the question used a starting compound of 2-aminocyclohexanol rather than 2-hydroxycyclohexanone. Let’s assume that the starting material isThen the diazonium salt is formed
Step 2: Reduction of Diazonium salt. The second step involves the reaction of the diazonium salt (A) with ammonium hydrosulfide (NH4SH) in water. This re duces the diazonium salt to the corresponding amine, with nitrogen gas as a byproduct. So the final product B is 2-aminocyclohexanol.
The descending order of basicity of following amines is :
Choose the correct answer from the options given below :
Which of the following amine(s) show(s) positive carbamylamine test?
The correct order of basicity for the following molecules is:
Match the compounds given in List-I with the items given in List-II
Match List-I with List-II.
Choose the correct answer from the options given below :