Common Blind Spot: Intramolecular Reactions
So I bought a belt today (pleather, 75 cents at the Goodwill). and decided to show it off. This is me putting it together. This
Read moreDon’t Be Futyl, Learn The Butyls
There are four different types of “butyls”, and they all have their own name. In addition they each have a common name (“trivial name”) which
Read moreReagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride)
TsCl (p-toluenesulfonyl chloride) And MsCl (methanesulfonylchloride) As Reagents In Organic Chemistry In a blatant plug for the Reagent Guide, each Friday I profile a different reagent
Read moreReagent Friday: NBS (N-Bromo Succinimide)
N-Bromosuccinimide (NBS) As A Reagent In Organic Chemistry In a blatant plug for the Reagent Guide, each Friday I profile a different reagent that is commonly
Read moreReagent Friday: Chromic Acid, H2CrO4
H2CrO4 (Chromic Acid, a.k.a. the protonated form of K2Cr2O7 / Na2Cr2O7 / K2CrO4 / Na2CrO4) As A Reagent In Organic Chemistry In a blatant plug
Read moreGrossman’s Rule
A few months ago after putting up this post on “Hidden Hydrogens, Hidden Lone Pairs, and Hidden Counterions”, commenter Stewie Griffin made me aware of
Read moreThe Organic Chemistry Reagent Guide is here!
It’s taken a long time – late April through early May was hectic – but today I’m thrilled to finally announce the launch of the
Read moreWhy organic chemistry is hard (2)
Today’s post is about how a simple reaction can lead to all kinds of complications. I’m talking about the Grignard reaction here, although the principles
Read moreOrganic Chemistry Study Tips: Super-Detailed Advice
The other day a student named Peter left several comments about his specific study methods in organic chemistry. I thought it was so useful that
Read moreThionyl Chloride (SOCl2)
Thionyl Chloride, SOCl2 – Reaction With Carboxylic Acids to Give Acid Halides Thionyl chloride (SOCl2) is a useful reagent for converting carboxylic acids to acid chlorides.
Read more