In the last post, we mentioned that one of the consequences of the fact that carbon can form rings is that small rings (less than 8 carbons) are so rigid that they can’t be turned inside out [video]. One of the …
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Imagine having a comprehensive online guide to help you solve your own problems in organic chemistry. That's my mission with this site. After earning a Ph.D. at McGill and doing a postdoc at MIT, I applied to be a professor. That didn't work out. So I decided to teach organic chemistry anyway. Master Organic Chemistry is the site I wish I had when I was learning the subject. -
Our New Book, "Practice Organic Mechanisms", Is OutPosted on: Mar 14, 2016
The Heck, Suzuki, and Olefin Metathesis Reactions (And Why They Don't Belong In Most Posted on: Mar 10, 2016
Gilman Reagents (Organocuprates): What They're Used ForPosted on: Feb 05, 2016
Gilman Reagents (Organocuprates): How They're MadePosted on: Jan 29, 2016
Grignard Reactions And Synthesis (2)Posted on: Jan 19, 2016
said in Reagent Friday: Chromic Acid, H2CrO4 - The reaction is usually run in acetone or other organic solvent. Whether or not an aldehyde is water soluble wo... →
said in Conversion of carboxylic acids to esters using acid and alcohols (Fischer Esterification) - How about in the case of mevalonate forming a cyclic ester to become mevalolactone? Mevalonate is in its carboxyl... →
said in Imines and Enamines - Ah! This makes so much sense! Might I suggest the Learn 6 reactions for the price of one article be linked? ... →
said in The Heck, Suzuki, and Olefin Metathesis Reactions (And Why They Don’t Belong In Most Introductory Organic Chemistry Courses) - I completely agree with your analysis, and your conclusion that these reactions shouldn't be taught as a part... →
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