The most basic compound among the following is:-a)Acetanilideb)Benzyla...
Basicity is inversely proportional to resonance of lone pair electrons. Benzylamine is more basic. The electron pairs do not involve in resonance in benzylamine. In other amines, there is delocalization of lone pair of electron on N atom on the ring. In acetanilide, the delocalization of lone pair of electrons on N atom is due to adjacent CO group.
Hence option (B) is the answer.
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The most basic compound among the following is:-a)Acetanilideb)Benzyla...
Basicity of compounds
In chemistry, the term "basicity" refers to the ability of a compound to donate a pair of electrons or accept a proton. A basic compound is one that can accept a proton and forms a conjugate acid. The basicity of a compound depends on the presence of electron-donating groups or atoms.
Comparing the compounds
To determine the most basic compound among the options given, let's compare their structures and identify any electron-donating groups or atoms.
a) Acetanilide:
Acetanilide is an organic compound that consists of an acetamide group attached to an aniline group. The aniline group contains a nitrogen atom, which can act as a lone pair donor. However, the presence of the acetyl group (-COCH3) attached to the nitrogen atom decreases its basicity. The acetyl group is an electron-withdrawing group, which decreases the availability of the lone pair of electrons on the nitrogen atom.
b) Benzylamine:
Benzylamine is an organic compound that consists of a benzyl group attached to an amino group (-NH2). The amino group contains a lone pair of electrons, which can act as a donor. The benzyl group is a relatively weak electron-donating group, but it does not significantly decrease the basicity of the amino group. Therefore, benzylamine is more basic than acetanilide.
c) p-Nitroaniline:
p-Nitroaniline is an organic compound that consists of an aniline group with a nitro group (-NO2) attached to the para position of the benzene ring. The nitro group is an electron-withdrawing group, which decreases the basicity of the amino group. Therefore, p-nitroaniline is less basic than both acetanilide and benzylamine.
d) Aniline:
Aniline is the simplest compound among the options given. It consists of a benzene ring attached to an amino group (-NH2). The amino group contains a lone pair of electrons, making aniline a basic compound. However, benzylamine is more basic than aniline because the benzyl group is a stronger electron-donating group than the phenyl group.
Conclusion
Among the given options, the most basic compound is benzylamine (option b). It has a relatively strong electron-donating group (benzyl group) attached to the amino group, which increases its basicity compared to the other compounds.
The most basic compound among the following is:-a)Acetanilideb)Benzyla...
Basicity is inversely proportional to resonance of lone pair electrons. Benzylamine is more basic. The electron pairs do not involve in resonance in benzylamine. In other amines, there is delocalization of lone pair of electron on N atom on the ring. In acetanilide, the delocalization of lone pair of electrons on N atom is due to adjacent CO group.
Hence option (B) is the answer.