November 21, 2024, 11:37:25 PM
Forum Rules: Read This Before Posting


Topic: Reactivity in EAS  (Read 3398 times)

0 Members and 1 Guest are viewing this topic.

Offline kahalla

  • New Member
  • **
  • Posts: 4
  • Mole Snacks: +0/-0
Reactivity in EAS
« on: April 29, 2010, 08:08:37 PM »
Which of the following substances are least reactive in EAS:

Benzene, Nitrobenzene, Ethylbenzene, Phenol, Phenoxide anion?

I know that the more stable the carbocation, the faster the reaction will proceed. I also know that nitrobenzene reacts faster than benzene, which excludes that one from the list. I also think I read somewere that phenol is very reactive in EAS. Maybe the phenoxide anion is slowest because it won't be very stable as a cation? Any help?

Offline Smrt guy

  • Full Member
  • ****
  • Posts: 101
  • Mole Snacks: +5/-4
Re: Reactivity in EAS
« Reply #1 on: April 29, 2010, 09:17:42 PM »
Electron rich aromatics react much faster than electron poor ones.  Which is the most electron poor?

Offline kahalla

  • New Member
  • **
  • Posts: 4
  • Mole Snacks: +0/-0
Re: Reactivity in EAS
« Reply #2 on: April 30, 2010, 12:21:37 AM »
In that case Penoxide anion is probably the one that reacts fastest. Ethylbenzene will be less electronrich than benzene, so ethylbenzene is probably correct then? Thanks!

Offline Smrt guy

  • Full Member
  • ****
  • Posts: 101
  • Mole Snacks: +5/-4
Re: Reactivity in EAS
« Reply #3 on: May 01, 2010, 01:17:58 PM »
Ethyl benzene is more e- rich than benzene.  What about nitrobenzene?

Sponsored Links