Geometrical isomerism (cis-trans isomerism) arises in compounds that have restricted rotation around a double bond or a ring system, typically involving alkenes or cyclic compounds where two substituents are attached to a double bond or ring.
- Option A: 2-methylbut-2-ene has a double bond between two carbon atoms (C=C) with different groups attached, making it a compound that can show cis-trans isomerism.
- Option B: 2-methylpropene has a double bond but the two groups on the same carbon (C=CH2) do not allow for cis-trans isomerism due to identical substituents.
- Option C: Cyclohexene does not exhibit cis-trans isomerism because its double bond is part of a cyclic structure, and there is no opportunity for the type of substitution that allows for such isomerism.
- Option D: 1,2-dibromopropene is a compound that exhibits geometrical isomerism. The bromine atoms are attached to different carbons of the double bond (C=C), and the two positions can lead to cis (both bromines on the same side) and trans (bromines on opposite sides) isomerism.
Thus, 1,2-dibromopropene shows geometrical isomerism.