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प्रश्न
Give reasons for the following:
CH3NH2 is more basis than C6H5NH2.
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उत्तर
Aromatic amines are far less basic than aliphatic amines. This can be explained as follows:
Resonance stabilisation is there in aniline. It can be regarded as a resonance hybrid of the following structures:

Hence, the lone pair of electrons on the nitrogen atom gets delocalised over benzene ring and thus is less available for protonation.
The electron density on the nitrogen atom is increased by electron-donating inductive effect of the alkyl groups. As a result, aliphatic amines are much stronger bases than aniline.
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संबंधित प्रश्न
Classify the following amine as primary, secondary or tertiary:
(C2H5)2NH
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[NaNO2/HCl][273 K] B ->[H2O][283 K] C}\] ‘C’ is:
Write a short note on the following.
Carbylamine reaction
Write a short note on the following.
Mustard oil reaction
Account for the following.
pKb of aniline is more than that of methylamine.
Account for the following.
Although amino group is o- and p-directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.
The following amine can be classified as (C2H5)2NH:
The amine formed from an amide by mean of bromine and alkali has how many number of carbon atoms?
Which among the following is the strongest Bronsted base?
Write a short note on the following.
Ammonolysis
