November 27, 2024, 05:49:04 PM
Forum Rules: Read This Before Posting


Topic: Birch reduction  (Read 2343 times)

0 Members and 3 Guests are viewing this topic.

Offline missUK11

  • Regular Member
  • ***
  • Posts: 55
  • Mole Snacks: +0/-4
Birch reduction
« on: November 03, 2012, 12:12:30 PM »
Hello all,

I know how do write a mechanism for the birch reduction of benzene, but would the mechanism be the exactly the same for the birch reduction of anthracene to 9,10-dihydroanthracene except that reduction would take place in the central ring because it is the region of highest electron density? 

Thanks.
« Last Edit: November 03, 2012, 01:07:06 PM by missUK11 »

Offline discodermolide

  • Chemist
  • Sr. Member
  • *
  • Posts: 5038
  • Mole Snacks: +405/-70
  • Gender: Male
    • My research history
Re: Birch reduction
« Reply #1 on: November 03, 2012, 12:21:26 PM »
Why should it be any different?
Development Chemists do it on Scale, Research Chemists just do it!
My Research History

Offline missUK11

  • Regular Member
  • ***
  • Posts: 55
  • Mole Snacks: +0/-4
Re: Birch reduction
« Reply #2 on: November 03, 2012, 01:06:10 PM »
I read somewhere that it produces a dianion so I wasn't too sure if that would change the mechanism a little.

Why should it be any different?

Sponsored Links