Electrophilic aromatic substitution. Part XII. The nitration of 1-acetamidonaphthalene in acetic anhydride, in acetic acid, and in sulphuric acid
S. R. Hartshorn, Keith Schofield
Abstract
S. R. Hartshorn, Keith Schofield
Abstract
The kinetics and products of nitration of 1-acetamidonaphthalene in the named solvents are presented. In acetic anhydride and in sulphuric acid the behaviour is similar to that observed for acetanilide, but in acetic acid, nitration occurs via nitrosation. Earlier results for the nitration of 1-acetamidonaphthalene are discussed.
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The kinetics and products of nitration of 1-acetamidonaphthalene in the named solvents are presented. In acetic anhydride and in sulphuric acid the behaviour is similar to that observed for acetanilide, but in acetic acid, nitration occurs via nitrosation. Earlier results for the nitration of 1-acetamidonaphthalene are discussed.
Key concepts: Nitration, Acetic anhydride, Acetanilide, Chemistry, Acetic acid, Electrophilic aromatic substitution, Electrophilic substitution, Nitrosation