The correct options are
A B
D Aromatic hydrocarbons are hydrocarbons containing sigma bonds and pi electrons between the carbon atom in a ring. According to the Huckel rule, ring having planarity, complete delocalization of the pi electrons, conjugation of double bonds, and the presence of
4n+2π electrons in the ring where n is an integer are aromatic compounds.
Thus,
are aromatic in nature. In option (b) and (d) lone pairs on
N atom and
O atom respectively takes part in the conjugation.
(a) For
n=1,
4n+2π=6π and benzene is having
6π electrons as can be seen from its structure. All double bonds are in conjuation and are in one plane. Hence, it is aromatic.
(b) For
n=1=6π electrons as the lone pair on nitrogen atom participate in conjugation. Hence, aromatic.
(c)
For this compound, there are only
4π electrons, as per huckel's rule (
4n+2π )electrons, keeping
n=0 we get,
2π electrons and keeping
n=1 we get
6π electrons but in the system , only
4π electrons are present. Hence, it is non-aromatic.
(d) Compound (d) contains
6π electrons as lone pair of oxygen takes part in conjugation, hence it is aromatic.