Abstract
Conversions of aliphatic chlorine-containing compounds (chloroalkenes, chloroalkanes, and derivatives of chloro-substituted carboxylic acids) occur under the action of aprotic acids. Chloroethylenes are polymerised by a cationic mechanism with the formation of oligomeric and polymeric products. The principal reaction of chloroalkanes and chlorocycloalkanes in the presence of salts of coordination-unsaturated metals is dehydrochlorination, which proceeds either intramolecularly or intermolecularly with the formation of polymers with conjugated double bonds. For polychloro-containing compounds, in addition to the dehydrochlorinations, elimination of chlorine occurs. Perchloroalkanes (from C3 and higher) in the presence of aprotic acids also undergo degradation with breaking of the carbon–carbon bond.
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