November 25, 2024, 01:36:24 AM
Forum Rules: Read This Before Posting


« previous next »
Pages: [1]   Go Down

Topic: Which reagent to use?  (Read 2298 times)

0 Members and 2 Guests are viewing this topic.

Offline noor123

  • Regular Member
  • ***
  • Posts: 54
  • Mole Snacks: +0/-0
Which reagent to use?
« on: October 15, 2014, 08:04:14 AM »
Does it work well to use H2O in Sn1 rxn?  Are there any other reagents that can be used?
Logged

Offline orgopete

  • Chemist
  • Sr. Member
  • *
  • Posts: 2636
  • Mole Snacks: +213/-71
    • Curved Arrow Press
Re: Which reagent to use?
« Reply #1 on: October 15, 2014, 08:40:58 AM »
Quote from: noor123 on October 15, 2014, 08:04:14 AM
Does it work well to use H2O in Sn1 rxn?  Are there any other reagents that can be used?

Could you use an SN2 mechanism? If not, why not.
Logged
Author of a multi-tiered example based workbook for learning organic chemistry mechanisms.

Offline noor123

  • Regular Member
  • ***
  • Posts: 54
  • Mole Snacks: +0/-0
Re: Which reagent to use?
« Reply #2 on: October 15, 2014, 09:22:36 AM »
what reagent do i use then?  Its tertiary...and i only know of sn1 rxn.
Logged

Offline Babcock_Hall

  • Chemist
  • Sr. Member
  • *
  • Posts: 5705
  • Mole Snacks: +330/-24
Re: Which reagent to use?
« Reply #3 on: October 15, 2014, 09:40:58 AM »
I would also give some thought to how one might tip the balance toward substitutions and away from eliminations.
Logged

Offline zsinger

  • Full Member
  • ****
  • Posts: 374
  • Mole Snacks: +18/-60
  • Gender: Male
  • Graduate Chemist
Re: Which reagent to use?
« Reply #4 on: October 16, 2014, 10:47:22 AM »
^^ What Babcock said.
Logged
"The answer is of zero significance if one cannot distinctly arrive at said place with an explanation"
Pages: [1]   Go Up
« previous next »
Sponsored Links