Important Notice: Our web hosting provider recently started charging us for additional visits, which was unexpected. In response, we're seeking donations. Depending on the situation, we may explore different monetization options for our Community and Expert Contributors. It's crucial to provide more returns for their expertise and offer more Expert Validated Answers or AI Validated Answers. Learn more about our hosting issue here.

Why dont tertiary alkyl halides undergo Wurtz reaction?

0
Posted

Why dont tertiary alkyl halides undergo Wurtz reaction?

0
adianadi adi

 Since the free radicals are formed during the wurtz reaction, those from tertiary halides may undergo elimination rather than SN2 required for getting alkane, the wurtz conditions for tertiary halides give alkenes rather than alkanes as expected.

 

Ref: http://www.adichemistry.com/organic/namedreactions/wurtz/wurtz-reaction-1.html

0

Tertiary alkyl halides dehydrohalogenate to give alkenes as the primary reaction presumably because this is the most favorable energetically stable structure.

Related Questions

What is your question?

*Sadly, we had to bring back ads too. Hopefully more targeted.

Experts123