Last post in this series we introduced the Diels-Alder reaction. We saw that no matter how complex the diene or dienophile, or no matter what substituents are attached, the pattern of bonds that form and break are alw…
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The Hofmann and Curtius RearrangementsPosted on: Sep 19, 2017
Reducing SugarsPosted on: Sep 12, 2017
Cyclic Dienes and Dienophiles in the Diels-Alder ReactionPosted on: Sep 08, 2017
Reductive AminationPosted on: Sep 01, 2017
The Diels-Alder ReactionPosted on: Aug 30, 2017
said in A Handy Rule of Thumb for Acid-Base Reactions - Generally not practical for pKa difference of >10. Absolutely not practical for NaCl and CH4. We're talking 55... →
said in A Handy Rule of Thumb for Acid-Base Reactions - What if the pka difference between an acid and base species is significantly greater than 10. I know the... →
said in The Hofmann and Curtius Rearrangements - Ha, very true statement about there being no narrative behind coverage of amines. I tend to frame them first a... →
said in Organic Chemistry IUPAC Nomenclature Demystified With A Simple Puzzle Piece Approach - Hi, I want to correct my previous comment (I double checked the IUPAC guidance) I got one detail wrong. Rul... →
said in Grossman’s Rule - I was one of the lucky ones to be part of Grossman's Organic chemistry course that taught writing reaso... →
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.
3 Trends That Affect Boiling Points
What Makes A Good Nucleophile?
Five Key Factors That Influence Acidity
Polar Protic? Polar Aprotic? Nonpolar? All About Solvents
Table of Functional Group Priorities for Nomenclature