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Organic Chemistry II • Intermediate
Can you explain how SN2 reactions work?
SN2 (Bimolecular Nucleophilic Substitution) is a one-step reaction where the nucleophile attacks the electrophilic carbon simultaneously as the leaving group departs.

Key points:
• Backside attack → Walden inversion
• Rate = k[substrate][nucleophile]
• Favoured with 1° carbons & strong nucleophiles
Give me a practice problem!
🧪 Problem: Predict the major product of the reaction between (R)-2-bromobutane and NaCN in DMSO...
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