Assertion (A): Diazonium salts of aromatic amines are more stable than those of aliphatic amines.
Reason (R): Diazonium salts of aliphatic amines show resonance.
Show Hint
- Both Assertion (A) and Reason (R) are true and Reason (R) is the correct explanation of the Assertion (A).
- Both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of the Assertion (A).
- Assertion (A) is true, but Reason (R) is false
- Assertion (A) is false, but Reason (R) is true.
The Correct Option is C
Solution and Explanation
Top Questions on Amines
- Which of the following is a primary amine?
- The correct order of basic strength of the following molecules is:
(A) \(\text{C}_6\text{H}_4\text{NH}_2\text{O}\)
(B) \(\text{C}_6\text{H}_4\text{NH}_2\text{MeO}\)
(C) \(\text{C}_6\text{H}_4\text{NH}_2\text{NO}_2\)
(D) \(\text{C}_6\text{H}_4\text{NH}_2\text{CH}_3\) - The product B formed in the following reaction sequence is: $$ {C}_6{H}_5{CN} \xrightarrow{{HCl}} (A) \xrightarrow{{AgCN}} (B) $$
- Identify correct statements: (A) Primary amines do not give diazonium salts when treated with \({NaNO}_2\) in acidic condition.
(B) Aliphatic and aromatic primary amines on heating with \({CHCl}_3\) and ethanolic \({KOH}\) form carbylamines.
(C) Secondary and tertiary amines also give 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: Amines have a lone pair of electrons on the nitrogen atom, due to which they behave as Lewis bases. Greater the value of \( K_b \) or smaller the value of \( pK_b \), stronger is the base. Amines are more basic than alcohols, ethers, esters, etc. The basic character of aliphatic amines should increase with the increase of alkyl substitution. However, it does not occur in a regular manner, as a secondary aliphatic amine is unexpectedly more basic than a tertiary amine in aqueous solutions. Aromatic amines are weaker bases than ammonia and aliphatic amines. Electron-releasing groups such as \( -CH_3 \), \( -NH_2 \), etc., increase the basicity, while electron-withdrawing substituents such as \( -NO_2 \), \( -CN \), halogens, etc., decrease the basicity of amines. The effect of these substituents is more pronounced at the para-position than at the meta-position.
(a) Arrange the following in increasing order of their basic character. Give reason:
\[ \includegraphics[width=0.5\linewidth]{ch29i.png} \]
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