First year mechanisms
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Redox Mechanisms
Displaying 32 mechanisms:
Redox- Oxidation- alcohol to ketone using CrO3
Redox- Oxidation- alcohol to aldehyde (DCC)- Pfitzner-Moffatt oxidation
Redox- Oxidation- alcohol to carbonyl- bromine water
Redox- Oxidation- alcohol to carbonyl- Dess Martin
Redox- Oxidation- alcohol to carbonyl- Oppenauer
Redox- Oxidation- alcohol to carbonyl- Swern Oxidation
Redox- Oxidation- Aldehyde to carboxylic acid using CrO3
Redox- Oxidation- alkene using Pb(OAc)4
Redox- Oxidation- alkenes to ketones (Wacker)
Redox- Oxidation- alkenes using SeO2 to form allylic alcohol
Redox- Oxidation- autoxidation using O2
Redox- Oxidation- formation of PCC (CrO3 equivalent)
Redox- Oxidation- oxidation of alkene to alcohol and amine using osmium compund
Redox- Oxidation- oxidation of alkene to alcohol and amine using Sharpless method
Redox- Oxidation- oxidation of alkene to allylic alcohol using CrO3
Redox- Oxidation- oxidation of alkene to diol using OsO4
Redox- Oxidation- oxidation of alpha-hydroxy carboxylic acid to aldehyde
Redox- Oxidation- oxidation of cyclohexene to cyclopentane aldehyde uisng thallium
Redox- Oxidation- oxidation of diol to dialdehyde using NaIO4
Redox- Oxidation- oxidation of diol using Pb(OAc)4
Redox- Oxidation- oxidation of phenol using Fe(III)
Redox- Oxidation- reaction of diol with CrO3
Redox- Oxidation- SeO2 oxidation of ketone
Redox- Reduction- Birch reduction of benzene
Redox- Reduction- Birch reduction- with carbonyl functional group
Redox- Reduction- Diborane reduction of carboxylic acids/amides
Redox- Reduction- Evans- beta hydroxy-ketone to 1,3-diol
Redox- Reduction- metal ammonia reduction of alpha-beta unsaturated ketone (trans-decalin)
Redox- Reduction- methylation of amines using formaldehyde and formic acid (Eschweiler-Clark)
Redox- Reduction- Red-Al? reduction of alkyne
Redox- Reduction- reduction of ester to ketone using DIBAL-H
Redox- Reduction- reduction of ketone- Meerwein-Pondorf-Verley reaction