Chemistry - Coordination Chemistry Question with Solution | TestHub

ChemistryCoordination ChemistryIsomerismMedium2 minQB
ChemistryMediummultiple choice

Select correct sketch(s) of opticaly active isomer of

Options:(select one or more)

Answer:
A, B
Solution:

To determine the optically active isomers of , we look for structures that lack a plane of symmetry (POS) or a center of inversion.

 

Solution:

Option (A) is correct: This is a cis-cis-cis isomer. The arrangement of ligands is asymmetrical, meaning no plane can divide the molecule into two identical halves, making it chiral and optically active.

 

Option (B) is correct: This is another cis-isomer configuration where the ethylenediamine (en) ring and other ligands are positioned such that there is no plane of symmetry. Like option (A), it is non-superimposable on its mirror image.

 

Option (C) is incorrect: In this sketch, the two Cl⁻ ligands are trans to each other (180° apart). This creates a vertical plane of symmetry passing through the Co and the en ring, rendering the molecule achiral and optically inactive.

 

Option (D) is incorrect: Here, the two NH₃ groups are trans to each other. This linear arrangement creates a plane of symmetry (the molecular plane containing Co, en, and Cl atoms), which makes the isomer optically inactive.

Stream:JEESubject:ChemistryTopic:Coordination ChemistrySubtopic:Isomerism
2mℹ️ Source: QB

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