Advanced Organic Chemistry: Reactions, Mechanisms, and Structure

acetic acyl addition alcohols aldehydes aldehydes or ketones aliphatic alkyl halides allylic amides amines ammonia Angew anhydrides aromatic rings aryl atom attack base benzene bromine carbanion carbon carbonium ion carboxylic acids catalyst CH₂ CH3 CH3 Chapter Chem chim chloride cleavage cleaved compounds conjugated COOH cyclic diazonium double bond electrons electrophilic elimination energy enol esters ethers example formed free radicals free-radical Friedel-Crafts give Grignard reagents H H H H₂O halogen hydrogen hydrolysis intermediate Interscience Publishers involves isomer ketones leaving group mechanism method methyl migration molecule nitriles nitro nitrogen nucleophilic substitution Olah olefins optically active orbital Organic Chemistry ortho oxidation oxygen pair phenols position prepared primary proton react reaction reactivity rearrangement reduction resonance salts secondary similar SN1 reactions sodium solvent species stable step steric structure substrate sulfonic sulfur tertiary Tetrahedron Letters tion trans treatment triple bonds usually York он