Answer:
Benzene is extraordinarily stable despite containing three double bonds because it does not behave like a normal polyunsaturated compound. Its stability is explained by the concept of resonance and aromaticity.
Reasons for the high stability of benzene:
Conclusion:
Thus, benzene is extraordinarily stable because of resonance stabilization and aromatic character, which make its electronic structure more stable than that of ordinary compounds containing multiple double bonds.
Consider the following sequence of reactions:
The major product $P$ is:
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.