Q.Identify the optically active compounds from the following:
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Start your 14-day free trial to unlock the full solution →Optical activity in coordination compounds arises from the absence of a plane of symmetry. Among the given complexes, only cis- and are optically active. The correct options are (i) and (iii).
Why optical activity matters here
Optical activity is a property of chiral molecules — those that are non-superimposable on their mirror image. In coordination chemistry, chirality usually appears when the complex lacks any plane of symmetry. The classic test: if you can draw a plane that cuts the complex into two mirror-image halves, the complex is achiral and optically inactive. If no such plane exists, the complex is chiral and can exist as a pair of enantiomers.
The ligands here are important:
- en (ethylenediamine) is a bidentate chelating ligand — it forms a ring with the metal.
- Cl and NH are monodentate.
Let’s examine each complex one by one.
1.
This is an octahedral complex with three bidentate en ligands. Each en ligand forms a five-membered chelate ring. The three rings are arranged around the cobalt ion.
Think of the geometry: the three en ligands wrap around the metal like a three-bladed propeller. This arrangement has no plane of symmetry — the complex is chiral. It exists as a pair of enantiomers (often called and forms).
Any octahedral complex with three identical bidentate ligands (like ) is always chiral — the propeller shape guarantees it.
So (i) is optically active.
2. trans-
Here, two en ligands occupy four positions in the octahedron, and the two Cl ligands are opposite each other (trans).
Draw the structure: the two en ligands lie in a plane, and the two Cl atoms are on opposite sides. This complex has several planes of symmetry — for instance, the plane that contains the metal and both Cl atoms, cutting through the middle of both en rings.
Because a plane of symmetry exists, the molecule is superimposable on its mirror image.
A common mistake is to think that chelate rings automatically create chirality. In the trans isomer, the symmetry of the Cl positions kills any chirality.
So (ii) is optically inactive.
3. cis- …
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