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If you start with an alkyl halide that is optically active (has chirality), an SN1 reaction will generate a
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- What are the conditions in the oxidation of secondary alcohols?
- substrates with different kinds of α-H's are used; LDA gives side reactions with aldehydes, and so they are unsuitable here
- 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