1- i think in mn 3 plus only1 d is vecant hybridisation is dsp3

2-justify this vbt doesnt make exact prediction regarding the tetrahedral and square planer str of 4- coordinated complex

3- justify and explain d orbitals splitting is inverted and is smaller as compare to octahedral field splitting

4- how dd transition helps in deciding the colour of complex

5- explain instability constant and compile complex

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2. According to valence bond theory, square planar complexes are formed only in case of central metal ion with configuration of (n-1)d8 or (n-1)d9.But this generalisation is not always true as for example the the complex [NiCl4]2- with d8 configuration is tetrahedral and not square planar.
So, it can be said that vbt doesnt make exact prediction regarding the tetrahedral and square planer structure of 4-coordinated complex.

4. d-d transition refers to the transition of electron/s from a lower energy t2g level to the higher energy eg level on absorption of light.When an electron in t2g d orbital absorbs light it gets excited and makes a transition to eg d orbital.If the light absorbed is in visible region, the transition complex appears coloured.Therefore, d-d transition helps in deciding the colour of complex.For example: in the complex [Ti(H2O)6]3+, Ti3+ ion has 3d1 configuration.The only electron in d orbital occupies t2g level in ground state.If this electron absorbs light in blue-green region, it gets excited to eg level and appears violet in colour.

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