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Real AI-generated output for "SN1 vs SN2 Reactions" — generated in 28 seconds.
SN1 vs SN2 Reactions
SN2 — Bimolecular Nucleophilic Substitution
Mechanism: One-step, concerted backside attack
Rate law: Rate = k[substrate][nucleophile]
Substrate: Methyl > 1° > 2° (3° never)
Stereochemistry: Complete inversion (Walden inversion)
Solvent: Polar aprotic (DMSO, DMF, acetone)
Nucleophile: Strong, unhindered (CN⁻, I⁻, OH⁻)
SN1 — Unimolecular Nucleophilic Substitution
Mechanism: Two-step — ionization then capture
Rate law: Rate = k[substrate] (nucleophile not in rate)
Substrate: 3° > 2° > 1° (methyl never)
Stereochemistry: Racemization (planar carbocation)
Solvent: Polar protic (water, methanol, ethanol)
⚠️ Common Exam Trap
2° substrates can go either SN1 or SN2 — answer depends on nucleophile strength and solvent.
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