Wittig Reaction
The Wittig Reaction
It is a reaction in which organophosphorus ylides react with aldehydes or ketones to give substituted alkenes. George Wittig was awarded the Nobel prize for this work in 1979. The most important advantage of alkene synthesis by this reaction is that the location of the double bond is absolutely fixed, as compare to the mixtures of alkenes produced by alcohol dehydration.
Course Material
- Resonance
- Resonance Effect
- Dipole Moment
- Iductive effect
- Hydrogen Bonding
- Nomenclature of Organic Compounds
- Alkanes and Cycloalkanes
- Alkenes and Alkynes
- Wittig Reaction
- Isomerism
- Isomerism I
- optical isomerism
- Aromatic Electrophilic Substitution Reactions
- Nucleophilic Substitution Reactions I
- Nucleophilic Substitution Reactions II
- Nucleophilic Substitution Reactions III
- Alcohols 1
- Alcohols 2
- Carboxylic Acid 1
- Carboxylic Acid 2
- Aldehyde and ketone
- Base catalyzed reactions of carbonyl compounds I
- Base catalyzed reactions of carbonyl compounds II
- Aldol Condensation
- Reactions of alkyl amines, Arene diazonium salts
- Unsaturated Hydrocarbons
- Chapters 26
- Department Biotechnology
- Teacher
Dr. Syed Gohar Taqi Kazimi