Abstract
1. The kinetics of the reaction of trans-β-chlorovinylmercury chloride with iodine was studied in nonpolar solvents-carbon tetrachlorine and benzene. 2. In nonpolar solvents the reaction proceeds without conservation of the geometrical configuration. Each of the isomers ofβ-chlorovinylmercury chloride gives the same equimolar mixture of trans- and cis-1,2-chloroiodoethylenes.
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