The E1 Reaction
The E1 Reaction – Three Key Pieces of Evidence, and a Mechanism Last time in this walkthrough on elimination reactions, we talked about two types
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 moreMy main goal at Master Organic Chemistry has always been to provide students with useful resources that they can’t easily find anywhere else. About six
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
Read moreElimination Reactions (E1) That Occur With Rearrangements – Hydride Or Alkyl Shifts Where there are carbocations (see last post), rearrangement reactions are never far behind.
Read moreThe E1cB (E1, Conjugate Base) Elimination Mechanism The E1cB (Elimination, Unimolecular, Conjugate Base) mechanism is a third mechanistic pathway for elimination reactions. In many ways
Read moreAlkyl Shifts In Carbocation Rearrangement Reactions, Including Ring Expansion Hydride shifts can sometimes occur when a more stable carbocation can be formed through migration of
Read more