Elimination Reactions (1): Introduction And The Key Pattern
Introduction to Elimination Reactions As you’ve probably noticed by now, organic chemistry is a lot different from physics. When we’re looking to predict what reaction
Read moreIntroduction to Elimination Reactions As you’ve probably noticed by now, organic chemistry is a lot different from physics. When we’re looking to predict what reaction
Read moreThe Williamson Ether Synthesis In the Williamson Ether Synthesis, an alkyl halide (or sulfonate, such as a tosylate or mesylate) undergoes nucleophilic substitution (SN2) by an alkoxide to give an ether.
Read moreSN1/SN2/E1/E2 – Summarizing The Key Factors That Determine Whether A Reaction Will Be SN1, SN2, E1 or E2 In this article we walk through the
Read moreElimination Reactions Are Favored By Heat Elimination reactions are often in competition with substitution reactions Generally speaking, adding heat tends to increase the proportion of elimination products relative
Read moreThe E1 Reaction – Three Key Pieces of Evidence, and a Mechanism Last time in this walkthrough on elimination reactions, we talked about two types
Read moreE2 Mechanism – How The E2 (Elimination, Biomolecular) Reaction Works Having gone through the E1 mechanism for elimination reactions, we’ve accounted for one way in
Read moreE1 versus E2 : Comparing The E1 and E2 Reactions Now that we’ve gone through the mechanisms of the E1 and E2 reactions, let’s take
Read moreAntiperiplanar Relationships Between C-H And The Leaving Group: The E2 Reaction and Cyclohexane Rings Here we come to a very testable application of the E2 reaction
Read moreElimination Reactions Using “Bulky Bases” – When The Zaitsev Product Is Minor We’ve recently talked about Zaitsev’s rule in elimination reactions, and how the transition
Read moreThe Important Role of The Counter-Ion In Determining E1 vs SN1 With tertiary alckyl halides, E1 will generally be favored over SN1 when heat is
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