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1. Stereoselectivity in E1 eliminations favors the E alkene product as substituents are farther apart in the anti-periplanar conformation, minimizing steric interactions. 2. In E2 eliminations, the anti-periplanar transition state is favored as it allows optimal orbital overlap while minimizing steric interactions between the base and the leaving group. 3. Stereospecific E2 eliminations from chiral starting materials give different alkene stereochemistry depending on the stereochemistry of the starting m

Author
rashid
Language
EN

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