Step 1: Basic idea.
According to Valence Bond Theory (VBT), the central metal ion in a coordination compound makes available a certain number of vacant orbitals (hybrid orbitals) for the formation of coordinate covalent bonds with ligands.
The ligands donate lone pairs of electrons into these vacant orbitals.
Step 2: Hybridisation concept.
- The type of hybridisation depends on the coordination number of the complex.
- For example:
- Coordination number 6 $\Rightarrow$ octahedral complexes $\Rightarrow$ \(d^2sp^3\) (inner orbital) or \(sp^3d^2\) (outer orbital).
- Coordination number 4 $\Rightarrow$ tetrahedral complexes $\Rightarrow$ \(sp^3\).
- Coordination number 4 $\Rightarrow$ square planar complexes $\Rightarrow$ \(dsp^2\).
Step 3: Example.
\([Co(NH_3)_6]^{3+}\): Cobalt in +3 oxidation state has 3d$^6$.
Pairing occurs to give empty \(d\)-orbitals.
Hybridisation is \(d^2sp^3\), leading to an octahedral geometry.
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\boxed{\text{VBT explains geometry, magnetic properties and bonding in coordination complexes.}}
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(i) Draw the diagram which indicates the splitting of d-orbitals in tetrahedral field.
(ii) Write any one limitation of valence bond theory.
(i)[Ni(CN)₄]²⁻ and [Ni(CO)(_4)] have different structures, but do not differ in their magnetic behaviour. Explain.
(ii) Write the formula of Tetraamineaquachloridocobalt(III)chloride.
(i) Write two postulates of Werner's coordination theory.
(ii) Draw the geometrical isomers of [(NH_3)_3(NO_2)_3] and give their structures.