By chlorination, i.e.
Long-continued treatment with halogens may, in some cases, result in the formation of aromatic compounds; thus perchlorbenzene, C 6 C1 6, frequently appears as a product of exhaustive chlorination, while hexyl iodide, C 6 H 13 I, yields perchlorand perbrom-benzene quite readily.
The chlorination or Plattner process, in which the metal is converted into the chloride, and the cyanide or MacArthur-Forrest process, in which it is converted into potassium aurocyanide.
As calciners they are used in tin mines and for the chlorination of silver ores.
Chlorination in glacial acetic acid solution yields pentachlor-m-diketo-R-hexene (2) and, at a later stage, heptachlor-m-diketo-R-hexene (3).
The ultimate chlorination product of copper, CuC1 2, when heated to redness, decomposes into the lower chloride, CuCI, and chlorine.
(3) Chlorination or Plattner Process.
Both fixed and rotating vats are employed, the chlorination proceeding more rapidly in the latter case; rotating barrels are sometimes used.
After charging, the barrel is rotated, and when the chlorination is complete the contents are emptied on a filter of quartz or some similar material, and the filtrate led to settling tanks.
This compound is readily oxidized to benzoic acid, C 6 H 5 000H, the aromatic residue being unattacked; nitric and sulphuric acids produce nitro-toluenes, C6H4 CH3 N02j and toluene sulphonic acids, C 6 H 4 CH 3 SO 3 H; chlorination may result in the formation of derivatives substituted either in the aromatic nucleus or in the side chain; the former substitution occurs most readily, chlor-toluenes, C 6 H 4 CH 3 Cl, being formed, while the latter, which needs an elevation in temperature or other auxiliary, yields benzyl chloride, C 6 H 5 CH 2 C1, and benzal chloride, C 6 11 5 CHC1 2.
By conducting the chlorination in alkaline solution, A.