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Since SN2 reactions are concerted, that means that this singular step is the
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- alkylation of enolate ions, aldol reactions compete, base can attack alkyl halide (SN2/E2)
- Br2 gives syn 3 membered ring with Br, water attacks more substituted carbon, deprotonation gives hydroxide, additional deprotonation gives an O electrophile, leaving group leaves and O binds to carbon that leaving group left
- LDA (or NAH... H2 product) can convert a carbonyl compound completely to its enolate, avoiding an equilibrium mixture of carbonyl compound and enolate