Two Important Reaction Patterns: Ortho- , Para- Directors and Meta- Directors It’s one thing to learn about electrophilic aromatic substitution reactions of benzene itself. But
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Ortho-, 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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Why are halogens ortho-, para- directors? All activating groups are also ortho-, para- directors. Halogens (F, Cl, Br, I) are notable in that they are deactivating ortho-, para- directors.
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How To Draw The Molecular Orbitals of The Allyl Cation, Allyl Radical And Allyl Anion Drawing the molecular orbitals of a pi system like allyl
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A Puzzle In The Basicity Of Some Disubstituted Aromatic Amines We’ve seen that several key factors influence the basicity of amines – charge, resonance, inductive
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Having gone through the mechanism of electrophilic aromatic substitution, explored activating and deactivating substituents, and seen the importance of directing groups, let’s now take the opportunity to
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Assigning R and S Configurations With the Cahn-Ingold-Prelog (CIP) Rules Enantiomers are stereoisomers that are non-superimposable mirror images of each other (by the way, molecules that are
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The Molecular Orbital Diagram of Butadiene, And How To Build It Butadiene is a conjugated diene consisting of two adjacent pi-bonds and comprised of 4 p-orbitals and
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Halogenation of Benzene via Electrophilic Aromatic Substitution Unlike alkenes, benzene does not undergo rapid chlorination or bromination with Cl2 or Br2 When it does undergo
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Aromatic rings undergo nitration and sulfonation through the electrophilic aromatic substitution mechanism. Aromatic rings can undergo nitration when treated with nitric acid HNO3 in addition to
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