Which of the following compounds can show geo | vedclass

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(D) For a compound to show geometrical isomerism,each carbon atom of the double bond must be attached to two different groups.In option $A$,the right

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(D) For a compound to show geometrical isomerism,each carbon atom of the double bond must be attached to two different groups.In option $A$,the right carbon is attached to two identical $Cl$ atoms,so it cannot show geometrical isomerism.In option $B$,the right carbon is attached to two identical $CH_3$ groups,so it cannot show geometrical isomerism.In option $C$,the left carbon is attached to $F$ and $Cl$ (different),and the right carbon is attached to two $Et$ groups (identical),so it cannot show geometrical isomerism.In option $D$,the ring carbon attached to the double bond has a $CH_3$ group and a ring bond (different),and the other ring carbon also has a $CH_3$ group and a ring bond. This structure allows for cis-trans isomerism due to the restricted rotation and different substituents on the ring carbons.

List-$I$ (Pair of Compounds)	List-$II$ (Type of Isomers)
$A$. $2-$Methylpropene and but$-1-$ene	$I$. Stereoisomers
$B$. $Cis-$but$-2-$ene and $trans-$but$-2-$ene	$II$. Position isomers
$C$. $2-$Butanol and diethyl ether	$III$. Chain isomers
$D$. But$-1-$ene and but$-2-$ene	$IV$. Functional group isomers

Which of the following compounds can show geometrical isomerism?

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