December 27, 2024, 03:36:31 AM
Forum Rules: Read This Before Posting


Topic: SN1  (Read 1858 times)

0 Members and 1 Guest are viewing this topic.

Offline Bassel

  • Regular Member
  • ***
  • Posts: 27
  • Mole Snacks: +0/-2
SN1
« on: December 06, 2013, 09:26:14 PM »
since it is an SN1 I first thought to look at the stabilities of the carbocat ions. since the are the same and there is no shifting I looked at the steric effect so i think that cpd A is the one reacting faster because it has less steric effect. is that true ? is it the right way of thinking in like these questions?

Offline orgopete

  • Chemist
  • Sr. Member
  • *
  • Posts: 2636
  • Mole Snacks: +213/-71
    • Curved Arrow Press
Re: SN1
« Reply #1 on: December 06, 2013, 09:37:22 PM »
I think the compound with higher energy, higher strain, will react faster.
Author of a multi-tiered example based workbook for learning organic chemistry mechanisms.

Offline Kate

  • Full Member
  • ****
  • Posts: 197
  • Mole Snacks: +8/-3
  • Gender: Female
Re: SN1
« Reply #2 on: December 07, 2013, 06:16:08 PM »
Yep, I think so too.

The best way to figure it out is to construct the chair conformation of A and B and see which one is less stable by looking at the axial position of Br. 

Offline rasoooool

  • New Member
  • **
  • Posts: 6
  • Mole Snacks: +0/-3
Re: SN1
« Reply #3 on: December 09, 2013, 09:01:16 PM »
Yep, I think so too.

The best way to figure it out is to construct the chair conformation of A and B and see which one is less stable by looking at the axial position of Br.
correction answer.

Sponsored Links