Another Exercise In Mind Reading
Here’s another great example of how one reagent used in a certain context performs one thing, and in a different context performs a completely different
Read moreHere’s another great example of how one reagent used in a certain context performs one thing, and in a different context performs a completely different
Read moreBetween posts on tautomerism and on lewis acid catalysis, I neglected to mention a really important point in carbonyl chemistry that illustrates another facet of
Read moreIn 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
Read moreIn a blatant plug for the Reagent Guide, each Friday I profile a different reagent that is commonly encountered in Org 1/ Org 2. Version 1.2
Read moreIn a blatant plug for the Reagent Guide, each Friday I profile a different reagent that is commonly encountered in Org 1/ Org 2. Version 1.2
Read moreToday, building on the previous 2-part series on mechanisms of anionic nucleophiles in carbonyl chemistry, I’m going to start looking at the reactions of the
Read moreLet’s talk about carbonyl chemistry today (aldehydes, ketones, carboxylic acids, and esters). Specifically, reaction mechanisms. If you look at the reaction mechanisms in detail you
Read moreAs part 4 of the most important reactions you learn in org 1, (acid-base, substitution, and addition) here’s an introduction to the elimination reaction. This
Read more(The last lesson in the series. I wish I had this series done by the time school started for most people, but I initially thought
Read moreOne thing has been missing from our discussion of acid-base reactions. Who cares? What does it matter that we understand acid base reactions? Why is
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