SN2 Reaction Explained (Organic Chemistry)
Автор: Joy Oyebisi Tutoring
Загружено: 2025-10-07
Просмотров: 45
This is an organic chemistry tutorial explaining SN2 Reaction and factors affecting SN2 reactions.
Even if there’s no stereochemistry involved, SN2 reactions still follow the same key principles:
✅ Backside attack of the nucleophile
✅ One-step mechanism (concerted reaction)
✅ Inversion of the bonding arrangement—if stereocenters were present
Think of it like opening a door: the nucleophile pushes from one side while the leaving group exits from the opposite side.
That’s the SN2 reaction in a nutshell!
But what really makes SN2 reactions unique?
✅ Strong nucleophile
✅ Polar aprotic solvent
✅ Less steric hindrance = faster reaction
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