The Aromaticity Rulebook, Aromatic Vs Antiaromatic Vs non-aromatic скачать в хорошем качестве

The Aromaticity Rulebook, Aromatic Vs Antiaromatic Vs non-aromatic

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! 🔥”