November 01, 2024, 02:33:02 PM
Forum Rules: Read This Before Posting


Topic: E2-Elimination reaction.  (Read 2954 times)

0 Members and 1 Guest are viewing this topic.

Offline Heli0x

  • Regular Member
  • ***
  • Posts: 21
  • Mole Snacks: +0/-0
E2-Elimination reaction.
« on: December 25, 2010, 05:09:11 PM »
I'm having trouble understanding why product nr.2 is formed, and not nr.1:



I'm guessing it has something to do with the E/Z-classification, though I'm not sure whether the Phenyl is to be interpreted as one unit, or to merely include the connected carbon from the ring.

If so then then, would that mean that the E formation, in which the methyl groups are trans-positioned, would dominate, rendering the second molecule the main one?

Offline Trave11er

  • Regular Member
  • ***
  • Posts: 25
  • Mole Snacks: +4/-0
Re: E2-Elimination reaction.
« Reply #1 on: December 26, 2010, 09:04:02 AM »
This because in order for E2 to proceed hydrogen and leaving group should be in kind of trans position to each other and when they are the 2. product is the only option.

Offline Heli0x

  • Regular Member
  • ***
  • Posts: 21
  • Mole Snacks: +0/-0
Re: E2-Elimination reaction.
« Reply #2 on: December 27, 2010, 06:09:01 AM »
Oh I see. Thank you very much.

Sponsored Links