Which of the following are aromatic?
Step 1: Aromaticity Conditions.
For a compound to be aromatic, it must satisfy Hückel's rule, which states that a molecule is aromatic if it has a planar ring structure with \( 4n + 2 \) π-electrons (where \(n\) is a non-negative integer).
Step 2: Analyze Each Compound.
- (A) This compound is not aromatic because it has 6 π-electrons (a common number for aromatic systems), but the ring is not planar, so it is not aromatic.
- (B) This compound has a nitrogen atom and a conjugated system, making it aromatic.
- (C) This compound contains a 6-membered ring with alternating single and double bonds, fitting the requirements for aromaticity with 6 π-electrons.
- (D) This compound has a conjugated system and satisfies the aromaticity condition with 6 π-electrons.
Step 3: Conclusion.
Thus, the aromatic compounds are (B), (C), and (D). The correct answer is (3).
Final Answer: \[ \boxed{\text{(3) B, C \& D}} \]
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.
A weight of $500\,$N is held on a smooth plane inclined at $30^\circ$ to the horizontal by a force $P$ acting at $30^\circ$ to the inclined plane as shown. Then the value of force $P$ is:
A steel wire of $20$ mm diameter is bent into a circular shape of $10$ m radius. If modulus of elasticity of wire is $2\times10^{5}\ \text{N/mm}^2$, then the maximum bending stress induced in wire is: