Question
For the complex ion , find:
- The oxidation state of cobalt
- The coordination number of cobalt
- The geometry of the complex
Solution — Step by Step
Let the oxidation state of Co be .
is a neutral ligand (oxidation state = 0). The overall charge of the complex ion is .
Setting up the equation:
The oxidation state of cobalt is +3, written as Co(III).
The coordination number is the number of ligand atoms directly bonded to the central metal atom.
is a monodentate ligand — it binds through its nitrogen atom (one donor atom per ligand). There are 6 NH₃ ligands, each contributing 1 bond.
For a coordination number of 6, the geometry is almost always octahedral — the 6 ligands arrange themselves at the corners of a regular octahedron around the central metal atom.
Co(III) with 6 NH₃ ligands forms a regular octahedral complex. The bond angles are all 90° (adjacent ligands) and 180° (opposite ligands).
Co has atomic number 27. Co³⁺ configuration: [Ar] (loses 3 electrons from 4s and 3d).
NH₃ is a strong field ligand (appears high in the spectrochemical series). In a strong field, the 3d electrons pair up:
All 6 electrons are paired → diamagnetic complex.
Hybridisation: (inner orbital complex — uses , , and orbitals).
Why This Works
The IUPAC rules for finding oxidation state follow simple algebra: sum of oxidation states = overall charge. Since NH₃ is neutral and doesn’t carry a charge, all the positive charge comes from cobalt.
The octahedral geometry for CN = 6 follows from VSEPR theory and the geometrical arrangement that minimises repulsion among 6 identical ligands — an octahedron achieves equal 90° angles between all adjacent ligands.
Common Mistake
Students often confuse oxidation state with coordination number. Oxidation state is determined by charge; coordination number is determined by number of bonds from ligands. In , the oxidation state is +3 (from charge calculation) and the coordination number is 6 (from counting ligand bonds). These are both 6 and 3 respectively — not the other way around.
For NEET and JEE: is a classic example of an inner orbital () octahedral complex. Contrast it with — F⁻ is a weak field ligand, giving outer orbital () hybridisation and a paramagnetic complex with unpaired electrons.