The Aromaticity Rulebook, Aromatic Vs Antiaromatic Vs non-aromatic
Автор: OrganiChemVerse
Загружено: 2025-10-30
Просмотров: 85
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Let’s decode Aromatic, Anti-Aromatic, and Non-Aromatic compounds
For a molecule to be aromatic, it must be:
👉 Cyclic,
👉 Planar,
👉 Fully conjugated, and
👉 Must have (4n + 2) π electrons — that’s Hückel’s Rule!
Example: Benzene (6 π electrons) — aromatic and super stable. 💫
Now, if it’s still cyclic, planar, and conjugated but has 4n π electrons,
it becomes anti-aromatic — highly unstable! ⚡
Example: Cyclobutadiene (4 π electrons).
And if it’s non-planar or not fully conjugated,
it’s non-aromatic — neither stable nor unstable due to aromaticity.
Example: Cyclooctatetraene bends out of plane to stay non-aromatic. 🌀
So remember the rule:
4n + 2 → Aromatic ✅
4n → Anti-aromatic ❌
Not planar/conjugated → Non-aromatic 😴
That’s aromaticity simplified — only on OrganiChemVerse! 🔥”
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