First year mechanisms:       Alkenes       Alkynes       Amines       Aromatic       Biological       Conjugate Addition       Enols and Enolates       Epoxides       Nucleophilic addition       Nucleophilic Substitution       Organohalides       Organometallics   Second year mechanisms   Third year mechanisms   All mechanisms   Books

Alkenes Mechanisms Displaying 21 mechanisms: Alkenes- addition of Br2 Alkenes- anti-dihydroxylation Alkenes- CCl3 and NaOH with alkene (carbene formation). Alkenes- Diels Alder- cycloaddition Alkenes- Diols from OsO4 to aldehydes (IO4/H2O) Alkenes- electrophilic addition of Br2 and H2O Alkenes- electrophilic addition of H2O Alkenes- electrophilic addition of HBr Alkenes- electrophilic addition of HBr (Hydride Shift) Alkenes- formation by dehydrogenation of alcohols Alkenes- formation by elimination of charged leaving group (Hoffman product) Alkenes- formation by elimination of HHal from RHal (E2) Alkenes- free radical addition of HBr Alkenes- hydroboration Alkenes- I2 AgOAc, AcOH (dry)- Prevost reaction. Alkenes- I2 AgOAc, AcOH (wet)- Woodward reaction Alkenes- organoboranes to alcohols Alkenes- oxymercuration to form alcohol Alkenes- ozonolysis Alkenes- Ozonolysis of cyclohexene (1,6 dialdehyde) Alkenes- syn-dihydroxylation (OsO4)