The Cyclohexane Chair Flip
The Cyclohexane Chair Flip All about how to draw the product of a cyclohexane chair flip – and also, three ways not to! The Two
Read moreThe Cyclohexane Chair Flip All about how to draw the product of a cyclohexane chair flip – and also, three ways not to! The Two
Read moreEnergy Diagram Of The Cyclohexane Chair Flip In the last post, we showed a video of a cyclohexane ring flip – turning a cyclohexane chair
Read moreEquatorial vs Axial Groups: Why The Equatorial Position Is Of Lower Energy Just to bring you up to speed, let’s quickly review the last post.
Read more“A-Values” For Substituted Cyclohexanes “A-Values” are a numerical way of rating the bulkiness of substituents on a cyclohexane ring. The “A-Value” represents the difference in
Read moreCarboxylic Acid to Ester Under Acidic Conditions (Fischer Esterification) The conversion of a carboxylic acid to an ester under acidic conditions is commonly known as
Read moreCarboxylic acids… are acids. I know that seems obvious. But it’s a near certainty that students taking Org 2 for the first time will forget
Read moreSpecial to MOC from Variety HOLLYWOOD, CA – Mirimax Entertainment announced today that they are suing educational organic chemistry website Master Organic Chemistry for an
Read moreFinding The Most Stable Conformation Of A Cyclohexane Chair You’re given a structure with two or more substituents on a cyclohexane ring, and you’re asked
Read moreWhy Is trans-Decalin More Stable Than cis-Decalin? At the beginning of this series I said that the fact that carbon can form rings leads to
Read moreIn the last post we talked about how having a great memory is no guarantee of doing well on many types of organic chemistry exams.
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