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
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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)