![Reagent Friday: LiAlH[Ot-Bu]3](https://11452-presscdn-0-51-pagely.netdna-ssl.com/wp-content/uploads/2011/11/1-thumbnail.png "Reagent Friday: LiAlH[Ot-Bu]3")
In a blatant plug for the Reagent Guide and the Reagents App for iPhone, each Friday I profile a different reagent that is commonly encountered in Org 1/ Org 2. Today’s reagent is probably a bit on the o…
-
The Hofmann EliminationPosted on: Oct 18, 2017
Hybrid OrbitalsPosted on: Oct 10, 2017
Activating and Deactivating Groups In Electrophilic Aromatic SubstitutionPosted on: Sep 26, 2017
The Hofmann and Curtius RearrangementsPosted on: Sep 19, 2017
Reducing SugarsPosted on: Sep 12, 2017
said in Don’t Be Futyl, Learn The Butyls - They are "common wrong names". As I wrote, they should be commented (and encourage people not to use them). →
said in Reagent Friday: Sodium Amide (NaNH2) - I think example 2 is a bit misleading. Although two equivalents of NaNH2 can result in some of the alkyne, it... →
said in Common Mistakes with Carbonyls: Carboxylic Acids… Are Acids! - Hydroxyl groups (OH), thiols (SH), and generally any other mildly acidic functional groups. Carboxylic acids ar... →
said in Bromination of alkenes with Br2 to give dibromides - I take issue with your incomplete curly arrows for the formation of the cyclic bromonium ion. You've missed a... →
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