A compound is said to be aromatic if it satisfies the following three conditions:
(i) It should have a planar structure.
(ii) The π-electrons of the compound are completely delocalized in the ring.
(iii) The total number of \(\pi\)-electrons present in the ring should be equal to \((4n + 2)\), where \(n = 0, 1, 2\) … etc. This is known as Huckel's rule.
Which of the following are aromatic?

Give plausible explanation for:
(a) Diazonium salts of aromatic amines are stable.
(b) Aniline does not undergo Friedel-Crafts reaction.
(c) Aniline on nitration gives substantial meta product.
Figure 8.9 shows the strain-stress curve for a given material. What are (a) Young’s modulus and (b) approximate yield strength for this material?

Two identical ball bearings in contact with each other and resting on a frictionless table are hit head-on by another ball bearing of the same mass moving initially with a speed V. If the collision is elastic, which of the following (Fig. 5.14) is a possible result after collision ?

Aromatic hydrocarbons, sometimes known as arenes, are aromatic organic molecules made up entirely of carbon and hydrogen. In aromatic compounds a benzene ring which is named after the simple aromatic chemical benzene, or a phenyl group when part of a larger structure, is the configuration of six carbon atoms.
Read More: Aromaticity
This reaction involves the replacement of one substituent on the ring of an aromatic hydrocarbon, commonly a hydrogen atom, by a different substituent group.
The common types of aromatic substitution reactions are:
In these types of reactions, the coupling of two fragments that have a radical nature is achieved with the help of a metal catalyst