In the last post we introduced the concept of aromaticity, a property of some unusually stable organic molecules such as benzene. Although some aromatic molecules are indeed fragrant (hello, vanillin! ) the term &#…
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Reactions of Sugars: Glycosylation and ProtectionPosted on: Apr 24, 2018
Electrophilic Aromatic Substitutions (1) - HalogenationPosted on: Apr 18, 2018
Molecular Orbitals in the Diels Alder ReactionPosted on: Mar 23, 2018
Disubstituted Benzenes: The Strongest Electron-Donor "Wins"Posted on: Mar 19, 2018
Why are halogens ortho- para- directors?Posted on: Mar 05, 2018
said in Reagent Friday: Grignard Reagents - Oxygen, yes, although it should be protected as an ether and not have O-H. Nitrogen also possible but on comple... →
said in Reagent Friday: Grignard Reagents - Is it possible to synthesize Grignard using an organic compound that has nitrogen or oxygen? →
said in The Malonic Ester Synthesis - Why is this reaction called a Malonic ester "synthesis"? We're starting with a malonic ester and ending up w... →
About Master Organic Chemistry
After doing a PhD in organic synthesis at McGill and a postdoc at MIT, I applied for faculty positions at universities and it didn’t work out, yada yada yada. So I decided to teach organic chemistry anyway! Master Organic Chemistry is the resource I wish I had when I was learning the subject.
What Makes A Good Nucleophile?
3 Trends That Affect Boiling Points
Five Key Factors That Influence Acidity
Polar Protic? Polar Aprotic? Nonpolar? All About Solvents
Table of Functional Group Priorities for Nomenclature