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Stereoisomeric olefins, cycloalkanes, etc. which differ in the positions of groups relative to a reference plane: in the cis-isomer the atoms are on the same side, in the trans-isomer they are on opposite sides. An obsolete synonym, for which the usage is strongly discouraged, is geometric isomerism.

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Why is cis-1,2-dichloroethene more stable than trans-1,2-dichloroethene?

In this answer, I will point out an inadequacy of the reasoning based on resonance structures and I will also provided another MO perspective, which I believe is more convincing, on the issue. A fla …
Tan Yong Boon's user avatar