destroyer OG

This forum made possible through the generous support of SDN members, donors, and sponsors. Thank you.

Nano242

New Member
10+ Year Member
15+ Year Member
Joined
Jul 31, 2007
Messages
2
Reaction score
0
Points
0
  1. Pre-Dental
Advertisement - Members don't see this ad
Hi everyone,
I have a question regarding organic chemistry in destroyer... question # 97..
can any one explain to me how does this reaction work? I am not quite sure about the answer.. please help me!!!
 
Hi everyone,
I have a question regarding organic chemistry in destroyer... question # 97..
can any one explain to me how does this reaction work? I am not quite sure about the answer.. please help me!!!

First off, assume you are saturated in CH3MgCl.

1 mole attacks and the carbonyl turns into O-.

The O- reforms the carbonyl and kicks off the -OCH3 group because that is the most stable form. Now you have a ketone.

Another mole attacks the ketone and the O- is protonated with H30+ resulting in t-butyl alcohol.
 
Top Bottom