Aromatic Synthesis (1) – “Order Of Operations”
Planning An Aromatic Synthesis: Putting Reactions In The Right Order When planning a synthesis of simple aromatic compounds, it’s not enough to pick the right
Read morePlanning An Aromatic Synthesis: Putting Reactions In The Right Order When planning a synthesis of simple aromatic compounds, it’s not enough to pick the right
Read moreAzide Ion: Structure, Properties, and Substitution Reactions Table of Contents The Azide Ion Is A Great Nucleophile Organic Azides As “Masked” Amines Exploding On The
Read moreSynthesis of Benzene Derivatives: Converting ortho-,para- directors into meta- directors and vice versa. In planning the synthesis of simple benzene derivatives and other aromatic compounds,
Read moreMan, is there ever a lot of sugar nomenclature to know! This post aims to provide single place giving you the definitions of terms like
Read moreThe Haworth Projection The Haworth Projection is a convenient notation for showing the structure of sugars. Since every substituent points either straight up or straight
Read more“s-cis and s-trans conformations of dienes.” What does those terms mean? The “s–cis” is a conformation where both double bonds are on the same side
Read moreThe Sulfonyl Blocking-Group Strategy For Synthesis of Aromatic Molecules Or, how to just get the “ortho” product without any para- . Table of Contents Why
Read moreThe Hofmann Elimination Of Alkylammonium Salts: Examples and Mechanism The Hofmann Elimination is an elimination reaction of alkylammonium salts that forms C-C double bonds [pi
Read moreToday’s post is all about hybrid orbitals. Here’s a quick summary: [Note: This post was co-authored with Matthew Pierce of Organic Chemistry Solutions. Ask Matt about scheduling
Read moreBirch Reduction of Electron-Rich and Electron-Poor Aromatic Molecules – Examples and Mechanisms The Birch Reduction is a process for converting benzene (and its aromatic relatives)
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