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When an elimination reaction occurs to give the more stable, highly substituted alkene, we say the elimination reaction follows
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- to describe the proximity of atoms to the carbonyl center (which isn't given a Greek letter designation!
- convert more hindered alcohol into alkoxide, less hindered to its tosylate/alkyl halide, make sure tosylate/halide is a good SN2 substrate
- a nucleophilic enolate anion, which then attacks the electrophilic halogen molecule