To address the provided statements about the basicity of ethylamine compared to ammonia, we need to consider both the assertion and the reason:
Assertion (A):Ethylamine is indeed a stronger base than ammonia. This is because the ethyl group in ethylamine has an electron-donating nature, which increases the electron density on the nitrogen atom. This increased electron density makes it easier for ethylamine to donate a pair of electrons, enhancing its basicity compared to ammonia.
Reason (R):The statement suggests that the $-$I effect (inductive effect) of the ethyl group is responsible for the increased basicity. However, this is incorrect because the ethyl group actually shows a $+$I effect, meaning it donates electrons rather than withdrawing them. The positive inductive effect contributes to the electron-donating property, strengthening the base.
Based on this, while the assertion about ethylamine's basicity is correct, the reason provided is incorrect. The increased basicity is due to the $+$I effect of the ethyl group rather than the $-$I effect.
Therefore, the correct answer is: A is correct but R is incorrect.
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.
Which of the following amine(s) show(s) positive carbamylamine test? 