Aromaticity is determined based on Hückel's Rule, which states that a molecule is aromatic if it:
The species that satisfy all conditions for aromaticity (planar, cyclic, conjugated, and having \(4n + 2\) π electrons) are structures I, II, and IV.
Therefore, the correct answer is Option (D): I, II and IV.
To determine which of the following species are aromatic, we must apply Hückel's rule, which states that a molecule is aromatic if it is cyclic, planar, fully conjugated, and has 4n + 2 π-electrons, where n is a non-negative integer.
I: This is a benzene ring (C₆H₆), which is aromatic. It is cyclic, planar, fully conjugated, and has 6 π-electrons (n = 1).
II: This is cycloheptatrienyl cation (C₇H₇⁺), which is aromatic. It has 6 π-electrons (n = 1) and is planar and conjugated.
III: This is a benzene ring with a single bond (C₆H₆), which is not aromatic because the conjugation is disrupted by the single bond.
IV: This is a cyclopropenyl cation (C₃H₃⁺), which is aromatic. It has 4 π-electrons (n = 1) and is planar and conjugated.
V: This is a cyclohexane ring, which is not aromatic because it does not have a conjugated π-system.
Thus, the aromatic species are I, II, and IV.
Hence, the correct answer is (D) I, II, and IV.
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.