Which of the following are aromatic?

Condition 1: Aromaticity Criteria.
A compound is aromatic if it adheres to Hückel's rule: a planar ring structure with \( 4n + 2 \) π-electrons, where \(n\) is any non-negative integer.
Condition 2: Individual Compound Evaluation.
- (A) Not aromatic. Although it possesses 6 π-electrons, its non-planar ring disqualifies it.
- (B) Aromatic. The presence of a nitrogen atom and a conjugated system confirms its aromaticity.
- (C) Aromatic. Features a 6-membered ring with alternating single and double bonds, meeting aromaticity requirements with 6 π-electrons.
- (D) Aromatic. Exhibits a conjugated system and satisfies aromaticity criteria with 6 π-electrons.
Condition 3: Determination.
Therefore, compounds (B), (C), and (D) are aromatic. The correct choice is (3).
Final Determination: \[ \boxed{\text{(3) B, C \& D}} \]
Consider the following sequence of reactions:
The major product $P$ is:
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.