Nucleophile Substitution in der 1,3,5-Triazinreihe. IX. Kinetik und Mechanismus der Reaktion von Cyanurchlorid mit 4′-substituierten 4-Aminoazobenzenen

Nucleophilic Substitutions in 1,3,5-Triazines. VII. The Kinetic and ¦ Mechanism of Cyanuric Chloride with 4′-Substituted 4-Aminoazobenzens The kinetic and mechanism of cyanuric chloride reaction with 4′-substituted 4-aminoazobenzens in dioxan-water was studied by conductometry. An addition-elimination mechanism with a monomolecular elimination of chlorine ion at low water concentrations or a nucleophilic attack of 4-aminoazobenzens at high water concentration as low step has been supported by experimental data.