Aromaticity is determined based on Hückel's Rule, which states that a molecule is aromatic if it:
- is planar, cyclic, and conjugated.
- has \(4n + 2\) π electrons (where \( n = 0,1,2,3, \dots \)).
Analyzing the given species:
- Structure I: Aromatic (benzene-like), planar cyclic conjugated system with 6 π electrons (\(4(1) + 2 = 6\)), satisfies Hückel's rule.
- Structure II: Aromatic, typically represents a planar cyclic conjugated ion (e.g., cyclopentadienyl anion) with 6 π electrons, satisfies Hückel's rule.
- Structure III: Non-aromatic or antiaromatic (doesn't fulfill Hückel's rule, usually due to non-planarity or not having \(4n+2\) electrons).
- Structure IV: Aromatic (likely represents tropylium ion, cycloheptatrienyl cation), planar cyclic conjugated system with 6 π electrons (\(4(1) + 2 = 6\)), satisfies Hückel's rule.
- Structure V: Non-aromatic or antiaromatic, does not fulfill the aromaticity criteria.
Conclusion:
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.