(i) Enantiomers: Enantiomers are pairs of molecules that are non-superimposable mirror images of each other. They have identical physical properties but differ in their interaction with plane-polarized light and in the way they interact with other chiral substances. For example, the right- and left-handed forms of a chiral molecule are enantiomers.
(ii) Racemic mixture: A racemic mixture is a mixture containing equal amounts of two enantiomers of a chiral compound. In a racemic mixture, the optical activities of the enantiomers cancel each other out, resulting in no net optical rotation.
Given below are two statements:
Statement (I):
are isomeric compounds.
Statement (II):
are functional group isomers.
In the light of the above statements, choose the correct answer from the options given below:


The incorrect statements regarding geometrical isomerism are:
(A) Propene shows geometrical isomerism.
(B) Trans isomer has identical atoms/groups on the opposite sides of the double bond.
(C) Cis-but-2-ene has higher dipole moment than trans-but-2-ene.
(D) 2-methylbut-2-ene shows two geometrical isomers.
(E) Trans-isomer has lower melting point than cis isomer.
Calculate the angle of minimum deviation of an equilateral prism. The refractive index of the prism is \(\sqrt{3}\). Calculate the angle of incidence for this case of minimum deviation also.