November 27, 2024, 05:40:24 AM
Forum Rules: Read This Before Posting


« previous next »
Pages: [1]   Go Down

Topic: Condensation mechanism for formation of Tetraphenylcyclopentadienone  (Read 6005 times)

0 Members and 1 Guest are viewing this topic.

Offline amk5462

  • Very New Member
  • *
  • Posts: 1
  • Mole Snacks: +0/-0
Condensation mechanism for formation of Tetraphenylcyclopentadienone
« on: December 07, 2010, 12:46:28 AM »
I'm having a lot of trouble trying to figure of the mechanism for the reaction of 1,3-diphenylacetone with benzil to form tetraphenylcyclopentadienone. Triethylene glycol is the solvent and the base catalyst is Triton B (benzyl trimethylammonium hydroxide)
Logged

Offline Dan

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 4716
  • Mole Snacks: +469/-72
  • Gender: Male
  • Organic Chemist
    • My research
Re: Condensation mechanism for formation of Tetraphenylcyclopentadienone
« Reply #1 on: December 07, 2010, 04:01:53 AM »
Think about the reactivity of ketones, what can happen when you put them in base?
Logged
My research: Google Scholar and Researchgate
Pages: [1]   Go Up
« previous next »
Sponsored Links