What is the Difference Between Wittig Reaction and Wittig Rearrangement?
🆚 Go to Comparative Table 🆚The Wittig reaction and Wittig rearrangement are both important chemical reactions in organic chemistry. They are named after Nobel Prize-winning chemist Georg Wittig. Here are the key differences between the two:
Wittig Reaction:
- The Wittig reaction is a coupling reaction that involves the coupling of aldehydes.
- It is useful in the production of alkenes in organic synthesis processes.
- The nature of the produced alkene depends on the stability of the ylide, with unstabilized ylides giving Z-alkenes and stabilized ylides giving E-alkenes.
- The formation of E-alkenes is highly selective in this reaction.
Wittig Rearrangement:
- The Wittig rearrangement is a transformation of one form into another form depending on the stability.
- There are two main types of Wittig rearrangement: 1,2-Wittig rearrangement and 2,3-Wittig rearrangement.
- The 1,2-Wittig rearrangement involves the rearrangement of an ether with an alkyllithium compound, forming an alkoxy lithium salt as an intermediate and an alcohol as the final product.
- When the ether contains a good leaving group and electron-withdrawing group, such as a cyanide group, this group is eliminated during the rearrangement, forming the corresponding ketone.
In summary, the Wittig reaction is a coupling reaction used to produce alkenes, while the Wittig rearrangement is a transformation reaction involving the rearrangement of ethers.
Comparative Table: Wittig Reaction vs Wittig Rearrangement
The Wittig reaction and Wittig rearrangement are both important processes in organic chemistry, but they have distinct differences. Here is a comparison table highlighting their key differences:
Feature | Wittig Reaction | Wittig Rearrangement |
---|---|---|
Purpose | Forms alkenes from aldehydes and ketones | Involves the rearrangement of an ether |
Mechanism | Coupling reaction between aldehydes or ketones and a phosphorus ylide | Rearrangement of an ether with the formation of an alkoxy lithium salt as an intermediate |
Final Product | Alkenes | Ketones |
Types | Unstabilized ylides give Z-alkenes; stabilized ylides give E-alkenes | 1,2-Wittig rearrangement and 2,3-Wittig rearrangement |
The Wittig reaction is widely used in organic synthesis for the preparation of alkenes, while the Wittig rearrangement is a transformation of one form into another form depending on the stability of the ylide.
- Wittig vs Wittig Horner Reaction
- Cope vs Claisen Rearrangement
- Synthesis Reaction vs Substitution Reaction
- Sandmeyer Reaction vs Gattermann Reaction
- Hofmann vs Curtius Rearrangement
- SN1 vs SN2 Reactions
- Addition vs Substitution Reaction
- Gattermann vs Gattermann Koch Reaction
- Metathesis vs Redox Reactions
- Synthesis Reaction vs Dissociation Reaction
- Reductive Amination vs Transamination
- Oxidative Addition vs Reductive Elimination
- Catalytic vs Stoichiometric Reagents
- Finkelstein vs Swarts Reaction
- Elimination vs Substitution Reaction
- Electrocyclic vs Cycloaddition Reaction
- Oxidation Reaction vs Reduction Reaction
- Stereospecific vs Stereoselective Reactions
- Resonance vs Tautomerism