Explanation: In the reaction of 2-Aminoanthraquinone from 2- Chloroanthraquinone, by the use of potassium chlorate and ammonium nitrate as oxidants, it is possible to obtain directly a 2-aminoanthraquinone of 97.5-98.5 per cent purity.

Explanation: The preparation of p-Nitroaniline in done in batch reactor.

Explanation: The magma consist of finely divided nitroaniline and ammonium chloride solution.

Explanation: In continuous production of nitroaniline, CK stands for water-cooled agitated vessel.

Explanation: Sodium Anthraquinone-2-sulfonate on amination in presence of oxidant produces 2-Aminoanthraquinone.

Explanation: The preparation of 2-aminoanthraquinone from “silver” salt i.e. Sodium Anthraquinone-2-sulfonate.

Explanation: The 2-aminoanthraquinone obtained by this process generally averages 99 per cent pure, by titration with sodium nitrite. The yields range from 90-94 per cent of the theoretical.

Explanation: Mono-, di-, and trimethylamines are obtained by the reaction of methanol with ammonia under a pressure of 50 atm at about 380-450°C, over an aluminium oxide catalyst.

Explanation: Trimethylamine forms a binary azeotrope not only with NH3, but with mono- and dimethylamines as well, and that mono- and dimethylamine mixtures, boiling about 14°C apart, can be conveniently separated by fractional distillation.

Explanation: Solubility is influenced not only by the solvent, but by the different basicities of the amines.

Explanation: The full form of TMMD is Tetramethylmethylenediamine.

Explanation: Hydroammonolysis of Acetone thus yields a mixture of mono-, di-, and triisopropylamines.

Explanation: The successful industrial preparation of amines by the ammonolysis of aromatic halides, alcohols, and sulfonic acids depends largely upon the proper functioning of the ammonia system.