Limitations of Wurtz Fittig Reaction
Wurtz Fittig Reaction has limitations:
- Exclusive synthesis of symmetric alkanes.
- Inability to synthesize methane through this method.
- Tertiary alkyl halides exhibit lower reactivity due to steric hindrance.
- Limited application in coupling aryl halides.
- Safety concerns associated with the use of highly reactive metals like sodium.
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