Enolates – Formation, Stability, and Simple Reactions
All about enolates Enolates can be formed through removing the proton on carbons adjacent to a carbonyl (i.e. the “alpha-carbon“). The resulting anions are much
Read moreAll about enolates Enolates can be formed through removing the proton on carbons adjacent to a carbonyl (i.e. the “alpha-carbon“). The resulting anions are much
Read moreKinetic versus Thermodynamic Enolates of Ketones Enolates have a lot in common with alkenes. They are flat and have a C-C pi bond. Zaitsev’s rule
Read moreAldol Addition and Condensation Reactions (Base-Catalyzed) The Aldol Addition reaction is the addition of an enolate to an aldehyde (or ketone). Heating with base can result
Read moreReactions of Enols – Aldol Condensation, Halogenation, Mannich Reaction In a previous post on keto-enol tautomerism, we described the keto and enol forms. In this
Read moreDegrees of Unsaturation (Index Of Hydrogen Deficiency) The molecular formula of a compound can give clues about its structure. The formula for an alkane follows
Read moreConjugation And Color Why are tomatoes red? Why are carrots orange? Why are egg yolks yellow? And… why is Vulcan blood green? OK, I’m not going
Read moreThe Reaction Map PDF from Master Organic Chemistry (MOC) is a 15-page summary of the key reactions in introductory organic chemistry.
Read moreUnderstanding UV-Vis Spectroscopy Will Make You More Fun At Parties In today’s post we’ll discuss why most molecules are colourless, introduce the useful technique of
Read moreIf you are an instructor and prefer to source your exam questions to the original literature, Organic Syntheses [1] is a great source of classic,
Read moreSeventeen new pages have been recently added to the Reaction Guide: Olefin Metathesis The Strecker Synthesis Birch Reduction Cope Rearrangement Claisen Rearrangement Addition of Organolithiums
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