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Explores nucleophilic substitutions through SN1 and SN2 mechanisms, stereochemical inversion, leaving group quality, and nucleophilicity determination.
Explores redox reactions of aldehydes, including Evans-Tishchenko, Cannizzaro, and Benzoin reactions, reduction of imines, and Wittig reaction variants.
Explores chemical kinetics, including reaction rates, transition state, and catalysts, emphasizing the impact of concentration and temperature on reaction rates.
