The Amide Functional Group: Properties, Synthesis, and Nomenclature
Synthesis, Nomenclature, and Properties Of The Amide Functional Group In this post, we’ll try to provide a broad overview of amides. We’ll provide a brief
Read moreSynthesis, Nomenclature, and Properties Of The Amide Functional Group In this post, we’ll try to provide a broad overview of amides. We’ll provide a brief
Read moreThe Michael Addition Reaction (and Conjugate Addition) The Michael reaction (sometimes “Michael Addition”) is the addition of an enolate to an electrophilic alkene, such as
Read moreQuantifying The Basicity Of Amines, Using “The pKa Of The Conjugate Acid”, a.k.a. “pKaH” How do you measure the basicity of an amine? Case in point:
Read moreActivating and Deactivating Groups in Electrophilic Aromatic Substitution The rate of electrophilic aromatic substitution (EAS) reactions is greatly affected by the groups attached to the
Read moreElectrophilic Aromatic Substitution: The Mechanism Electrophilic aromatic substitution (EAS) reactions proceed through a two-step mechanism. In the first step, the aromatic ring, acting as a
Read more5 Key Amine Basicity Trends What are the most important factors that affect the basicity of amines? Here are 5 key trends. Basicity increases with
Read moreBonding And Antibonding Orbitals For A Simple Pi Bond Two adjacent p-orbitals each containing an electron can overlap to form a pi-bond In a pi
Read morePyranoses , Furanoses, Straight-Chain Glucose, And Ring-Chain Tautomerism Sugars such as glucose exist in equilibrium between their open-chain form and various cyclic forms where an
Read moreTwo Important Reaction Patterns: Ortho- , Para- Directors and Meta- Directors It’s one thing to learn about electrophilic aromatic substitution reactions of benzene itself. But
Read moreOrtho-, Para– and Meta– Directors In Electrophilic Aromatic Substitution (EAS), some substituents on benzene will direct the electrophile E to the ortho– (1,2)and para– (1,4) positions. These
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