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Unformatted text preview: 3 for R = Br, Cl)) Nucleophiles relative strengths, basicity, reactivity Acids and Bases relative basicity and acidity Mechanism arrow pushing Retrosynthesis Resonance Carbocations (formation, factors affecting stability, etc) Leaving groups relative reactivity Lewis acids and bases Keto-enol tautomerization Stereochemistry Retention and inversion of configuration Syn and anti-addition to C=C bonds Hydroboration-Oxidation...
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This note was uploaded on 02/16/2010 for the course CHEM ORGANIC CH taught by Professor Dotsevisogah during the Spring '09 term at Cornell University (Engineering School).
- Spring '09