The correct options are
A
B
D ![](https://df0b18phdhzpx.cloudfront.net/ckeditor_assets/pictures/789080/original_11._Option_D.png)
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,
![](https://search-static.byjusweb.com/question-images/byjus/ckeditor_assets/pictures/789076/original_11._option_A.png)
![](https://search-static.byjusweb.com/question-images/byjus/ckeditor_assets/pictures/789077/original_11._Option_B.png)
![](https://search-static.byjusweb.com/question-images/byjus/ckeditor_assets/pictures/789080/original_11._Option_D.png)
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)
![](https://search-static.byjusweb.com/question-images/byjus/ckeditor_assets/pictures/789079/original_11._Option_C.png)
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.