
To determine the number of geometrical isomers for the given structure:
Identifying Stereocenters: The given structure contains three stereocenters, which influence the overall geometric configurations.
Counting Geometrical Isomers: The maximum potential geometric isomers can be calculated using the formula:
Total Geometrical Isomers = 2n
where n is the number of stereocenters. In this case:
23 = 8
However, due to symmetry in the molecule, some configurations are equivalent, reducing the number of unique geometrical isomers.
Final Count: Considering the symmetry and equivalent configurations, the total number of unique geometrical isomers for the given structure is 4.
To determine the number of geometrical isomers possible for the given structure, follow these steps:
Conclusively, the solution meets the provided range of 4,4. Thus, the number of geometrical isomers possible is 4.
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.
Consider the following sequence of reactions : 
Molar mass of the product formed (A) is ______ g mol\(^{-1}\).

In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by: