Wrapup: The Quick N’ Dirty Guide To SN1/SN2/E1/E2
The previous several posts dealt with an approach to solving substitution and elimination problems that can only be described as a Quick N’ Dirty Guide
Read moreThe previous several posts dealt with an approach to solving substitution and elimination problems that can only be described as a Quick N’ Dirty Guide
Read moreLike I said in the introduction to substitution reactions, organic chemistry is an empirical, experimental science. We make observations, and then try to reason backwards
Read moreFor nucleophilic substitution, the pattern of bonds that form and break is pretty straightforward. You break C-(leaving group) and you form C-(nucleophile). A straight swap. But
Read moreFollowing up on the 4 most important patters of reactions in Org 1, and introduction to acid-base reactions, here’s the second major pattern. It’s called
Read moreToday starts a new series of posts on walking through one of the key classes of reaction in organic chemistry: substitution reactions. The goal of
Read moreChemistry is an experimental science. There is no great Ramanujan of our discipline, who, starting with a simple set of premises, could derive and predict
Read moreHaving gone through the two different types of substitution reactions, and talked about nucleophiles and electrophiles, we’re finally in a position to reveal the mechanism
Read moreHaving gone through the mechanism of the SN2 reaction, let’s take a second and look at why it might be useful. In nucleophilic substitution reactions,
Read morePreviously we saw that there are two important classes of nucleophilic substitution reactions, which differ in their rate laws, dependence on substitution pattern, and the
Read moreOne of the key factors that determines whether a nucleophilic substitution reaction will happen or not is the identity of the leaving group. Previously, we’ve
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