April 25, 2024, 03:43:19 AM
Forum Rules: Read This Before Posting


Topic: enzymatic hydrolysis  (Read 3760 times)

0 Members and 1 Guest are viewing this topic.

Offline noda

  • Regular Member
  • ***
  • Posts: 18
  • Mole Snacks: +0/-0
enzymatic hydrolysis
« on: January 04, 2007, 07:59:04 PM »
I need your help someone can explain why in the enzymatic hydrolysis of racemic cis-lactone 7(table 1) at low conversion values one of the products is ester 7 (from ring fission) and in table 2 with trans-lactone 8 the only product was the lactonic acid( why there isn't ring fission)?
thank you and happy new year

Offline FeLiXe

  • Theoretical Biochemist
  • Chemist
  • Full Member
  • *
  • Posts: 462
  • Mole Snacks: +34/-7
  • Gender: Male
  • Excited?
    • Chemical Quantum Images
Re: enzymatic hydrolysis
« Reply #1 on: January 05, 2007, 06:32:41 AM »
my guess:

with the cis form the enzyme can attack from the side where only hydrogens are

in the trans form there are big groups on both sides. so the enzyme can't attack from either side

the ester is always accessible
Math and alcohol don't mix, so... please, don't drink and derive!

Sponsored Links