E1cB – Elimination (Unimolecular) Conjugate Base
The 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 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 moreFunctional Groups Summary Sheet I thought it would be good to make a summary sheet based on functional groups, so here one is: Functional Group
Read moreThe Pinacol Rearrangement The pinacol rearrangement is an acid-catalyzed rearrangement of 1,2-diols (vicinal diols) The acid serves to protonate one of the hydroxyl groups, which
Read moreOver at Med School Odyssey, the author recently wrote about finishing Org 1, and has a lot to share about his experiences with the course.
Read moreIntroduction to Nucleophilic Substitution Reactions Today starts a new series of posts on walking through one of the key classes of reaction in organic chemistry:
Read moreOne of the reasons why so many students find organic chemistry difficult is that the problem-solving methods required to succeed in the course take them
Read more[image photo credit: www.nyapplecountry.com] What does it take to be a great organic chemistry TA? A few weeks ago, Dan Coiro, a graduate of Rutgers
Read moreComparing Two Nucleophilic Substitution Reactions That Clearly Have Different Mechanisms Experiments tell us that nucleophilic substitution reactions generally fall into two main groups: In one group: The reaction
Read moreThe SN2 Reaction Mechanism Having gone through the two different types of substitution reactions, and talked about nucleophiles and electrophiles, we’re finally in a position
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