November 01, 2024, 02:28:51 AM
Forum Rules: Read This Before Posting


« previous next »
Pages: [1]   Go Down

Topic: mCPBA epoxidation products  (Read 4192 times)

0 Members and 1 Guest are viewing this topic.

Offline science123

  • Regular Member
  • ***
  • Posts: 47
  • Mole Snacks: +1/-2
mCPBA epoxidation products
« on: December 31, 2010, 04:21:53 PM »


Is it correct that we get two products? Why ? Is it because of formation of two new chiral centers?
Logged

Offline democanarchis

  • Regular Member
  • ***
  • Posts: 72
  • Mole Snacks: +9/-0
Re: mCPBA epoxidation products
« Reply #1 on: December 31, 2010, 04:57:00 PM »
No, it is not due to the number of chiral centres formed. The starting material is achiral and planar; nucleophilic attack by the alkene onto mCPBA could occur from either face of the compound, giving the two products.
Logged
Pages: [1]   Go Up
« previous next »
Sponsored Links