Aromaticity:
A compound is said to be aromatic if it shows special stability due to delocalisation of π-electrons.
Necessary conditions for a system to be aromatic:
1. Cyclic structure
The molecule must be cyclic so that π-electrons can be delocalised around a closed loop.
2. Planarity
The molecule must be planar (or nearly planar) so that effective overlap of p-orbitals can occur.
3. Complete conjugation
Each atom in the ring must have a p-orbital, resulting in continuous overlap and complete conjugation. This usually means all atoms in the ring are sp2 hybridised.
4. Hückel’s rule (4n + 2 rule)
The ring must contain (4n + 2) π-electrons, where n = 0, 1, 2, 3, …
Examples:
n = 0 → 2 π-electrons
n = 1 → 6 π-electrons
n = 2 → 10 π-electrons
Conclusion:
A system is aromatic only if it is cyclic, planar, fully conjugated and obeys Hückel’s (4n + 2) π-electron rule. Such systems are exceptionally stable.
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.