The Hofmann and Curtius Rearrangements
Here’s the thing about the coverage of “amines” in Org 2: there’s no narrative. Unlike most chapters, it doesn’t start with a set of concepts
Read moreHere’s the thing about the coverage of “amines” in Org 2: there’s no narrative. Unlike most chapters, it doesn’t start with a set of concepts
Read moreEverything you ever wanted to know about converting Fischer Projections to Haworth Projections, And Vice Versa Starting with a Fischer projection, it’s not too hard
Read moreThe Diels-Alder Reaction Is Awesome Today we’ll introduce a reaction I consider to be the most useful and powerful reaction in all of organic chemistry: the
Read moreCope Elimination The “Cope Elimination” is a reaction where an amine is oxidized to an intermediate called an “N-oxide“, which, when heated, acts as the
Read moreCyclic Dienes (e.g. Cyclopentadiene) and Cyclic Dienophiles In The Diels-Alder Reaction Last post in this series we introduced the Diels-Alder reaction. We saw that no
Read moreA Shortcut For Determining The Hybridization Of An Atom In A Molecule Here’s a shortcut for how to determine the hybridization of an atom in
Read moreSodium borohydride (NaBH4) For the Reduction of Aldehydes and Ketones Sodium borohydride (NaBH4) is a convenient source of hydride ion (H-) for the reduction of
Read moreFinally, Some Reactions Of Sugars: Glycosylation And Protection In this post we introduce some simple reactions of sugars, especially glycosylation and protection: Formation of “glycosides”
Read moreKiliani-Fischer Synthesis and the Ruff Degradation The Kiliani-Fischer Synthesis is a method for extending a carbohydrate chain by a single carbon. The Ruff Degradation is
Read moreReactions of Benzene and Aromatic Compounds: A Reaction Map (PDF) Let’s map out all of the reactions we’ve learned in this section on aromatic rings
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