Question
Question: Which of the following is the strongest base: A., the corresponding negative or positive charge is relayed through the carbon chain by the atoms belonging to it. This causes a permanent dipole to arise in the molecule and is referred to as the inductive effect.
Presence of the electron-donating group increases the basicity of the amines whereas the electron-withdrawing group decreases the basicity.
In the compounds A, B and C, the lone pair of electrons on the nitrogen atom is in resonance with the aromatic ring and is not available for donation to an acid. Hence, these compounds are weak bases.
In the compound D, due to the presence of methylene group between the amino group and the benzene ring, the resonance between the lone pair of electrons on N and the benzene ring is not possible. Hence, this lone pair can be readily donated and benzylamine is the strongest base among the given bases.
Thus, the correct answer to this question is option D.
Note:
Relative inductive effects have been experimentally in laboratories with Hydrogen as the reference, the order of increasing +I effect is, as follows: NH3+>NO2>SO2R>SO3H>CHO>CO>COOH>COCl>CONH2>F>Cl
>Br>I>OH>OR>NH2 >C6H5>CH=CH2>H