November 30, 2024, 07:33:35 AM
Forum Rules: Read This Before Posting


Topic: Friedel Crafts mechanism problem help  (Read 3971 times)

0 Members and 1 Guest are viewing this topic.

Offline michaelaaaaa

  • Very New Member
  • *
  • Posts: 1
  • Mole Snacks: +0/-0
Friedel Crafts mechanism problem help
« on: March 17, 2012, 01:21:13 AM »
http://26.media.tumblr.com/tumblr_m10jt7PUmr1qzof18o1_500.png

Ok so the problem is written at the top its a benzene with a och3 on it, you use reagents:
1. ch3co2coch3, AlCl3, CS2
2. HCl, H2O
to get the product (sorry the picture is so small)

my problem is I got the product before using the second step reagents (HCl, and H2O) so what is the function of the HCl and H2O?

Anyone?

Offline Potla

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Re: Friedel Crafts mechanism problem help
« Reply #1 on: March 21, 2012, 03:23:28 AM »
my problem is I got the product before using the second step reagents (HCl, and H2O) so what is the function of the HCl and H2O?
I think HCl and H2O means dil. H+, which acts as a catalyst for the process. In case of anhydrides, I think two moles of AlCl3 is required, one mole is used for liberating the acid chloride from the anhydride:
R-CO-O-CO-R + AlCl3 --> RCOCl +RCOOAlCl2.
The second mole, forms the sigma complex with C6H6OMe and then the O-Al-Cl3 might take H+ and liberate one mole of HCl. Then the complex may lose a proton to regain aromaticity, followed by which the Cl may (intramolecular) attack the -AlCl2, causing breakage of O-Al bond and C-Cl bond through a 4-membered transition state.
This may be possible. I don't really know if all of this is correct or not, since I am a beginner. Hope I could be of some help. :)

Sponsored Links