1,2-Dichloroethylene

The two compounds are isomers, each being colorless liquids with a sweet odor.

[4] cis-DCE, the Z isomer, is obtainable by the controlled chlorination of acetylene: Industrially both isomers arise as byproducts of the production of vinyl chloride, which is produced on a vast scale.

[6] These compounds have "moderate oral toxicity to rats".

[1] The dichloroethylene isomers occur in some polluted waters and soils, as the decomposition products of trichloroethylene.

Significant attention has been paid to their further degradation, e.g. by iron particles.

Skeletal formula of cis-1,2-dichloroethene
Skeletal formula of cis-1,2-dichloroethene
Skeletal formula of trans-1,2-dichloroethene
Skeletal formula of trans-1,2-dichloroethene
Ball-and-stick model of cis-1,2-dichloroethene
Ball-and-stick model of cis-1,2-dichloroethene
Ball-and-stick model of trans-1,2-dichloroethene
Ball-and-stick model of trans-1,2-dichloroethene