Tosylates And Mesylates
All About Tosylates and Mesylates By themselves, alcohols are poor leaving groups since the hydroxide ion (HO-) is a strong base The OH group can
Read moreAll About Tosylates and Mesylates By themselves, alcohols are poor leaving groups since the hydroxide ion (HO-) is a strong base The OH group can
Read moreSN1 / SN2 / E1 / E2 The Nucleophile / Base This article assumes you understand the mechanisms of the SN1/SN2/E1 and E2 reactions. For
Read moreMany students taking organic chemistry one day plan to write the Medical College Admission Test (MCAT). A common question students have for me is what
Read moreSN1 vs E1, and SN2 vs. E2: The Role Of Heat This article assumes you understand the mechanisms of the SN1/SN2/E1 and E2 reactions. For
Read moreSecondary Alkyl Halides With Strongly Basic Nucleophiles. The “Ask Your Instructor” Edition In the previous four articles in this series, we covered how to identify where
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 moreA Tale of Two Elimination Reaction Patterns Like I said in the introduction to substitution reactions, organic chemistry is an empirical, experimental science. We make
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 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
Read more