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.
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.
Arrange the following in increasing order of their basic strength in aqueous solution:
CH$_3$–NH$_2$, (CH$_3$)$_2$NH, (CH$_3$)$_3$N
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.