Wurtz-Fittig Reaction FAQs
What is Wurtz Fittig Reaction named after?
Wurtz Fittig Reaction is named after French Chemist Charles-Adolphe Wurtz and Wilhelm Rudolph Fittig
Is Catalyst used in Wurtz Fittig Reaction?
Typically no catalyst is used, but a strong base like sodium or potassium is required.
What does Wurtz Fittig Reaction synthesize?
Wurtz Fittig Reaction Synthesize substituted aromatic compound
What is key reagent in Wurtz Fittig Reaction?
Sodium metal act as key reagent in Wurtz Fittig Reaction
How Can Toluene be Prepared using Wurtz Fittig Reaction?
To prepare toluene with wurtz fittig reaction, we have to take a mixture of chlorobenzene and methyl chloride and react it with sodium metal in presence of dry ether
Wurtz-Fittig Reaction
Wurtz Fittig Reaction is a chemical process related to the classic Wurtz Reaction. It is primarily used to join alkyl and aryl halides, commonly chlorides, bromides, or iodides in the presence of sodium metal and dry ether. This reaction is similar to the Wurtz Reaction, and results in the formation of a new carbon-carbon bond and merge two smaller alkyl or aryl molecules into a larger one.
In this article, we will learn in detail about the Wurtz Fittig Reaction, its equation, example, uses, and comparison with the Wurtz and the Fittig Reaction.
Table of Content
- What is Wurtz Fittig Reaction?
- Wurtz Fittig Reaction Equation
- Wurtz-Fittig Reaction Mechanism
- Uses of Wurtz Fittig Reaction
- Limitations of Wurtz Fittig Reaction
- Wurtz Fittig Reaction Distinction