April 18, 2024, 04:59:31 PM
Forum Rules: Read This Before Posting


Topic: carbocation stability  (Read 4091 times)

0 Members and 1 Guest are viewing this topic.

Offline CLMZ

  • Very New Member
  • *
  • Posts: 1
  • Mole Snacks: +0/-0
carbocation stability
« on: March 22, 2010, 01:32:11 AM »
Need help in determining a logical reaction mechanism to explain the formation of the major and minor products for the reaction of alcohol 1 with HBr which gave 3-bromo-2,3-dimethylpentane as the major product and 2-bromo-3,4-dimenthylpentane as the minor product

Offline AC Prabakar

  • Full Member
  • ****
  • Posts: 109
  • Mole Snacks: +5/-1
  • Gender: Male
Re: carbocation stability
« Reply #1 on: April 01, 2010, 09:14:24 AM »
It will be helpful if i got the structure of alcohol to reply your question.

Offline Dan

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 4716
  • Mole Snacks: +469/-72
  • Gender: Male
  • Organic Chemist
    • My research
Re: carbocation stability
« Reply #2 on: April 01, 2010, 11:59:08 AM »
I assume the structure of the alcohol is unknown and you need to work its structure out from the products.

CLMZ - Look up 1,2 hydride shifts and carbocation rearrangements, there's tons of stuff on google and in any organic textbook - it's fairly straightforward from there.
My research: Google Scholar and Researchgate

Sponsored Links