Answer the following:
(i) What happens to the colour of the complex \([ \text{Ti(H}_2\text{O)}_6 ]^{3+}\) when heated gradually?
(ii) Write the electronic configuration for a \(d^5\) ion if \(\Delta_o < P\).
(iii) Write the hybridization and magnetic behaviour of the complex \([ \text{Ni(CO)}_4 ]\).
(Atomic number: Ni = 28)
(i) What happens to the colour of the complex \([ \text{Ti(H}_2\text{O)}_6 ]^{3+}\) when heated gradually?
Answer: The colour of the complex \([ \text{Ti(H}_2\text{O)}_6 ]^{3+}\) deepens when it is heated gradually. This occurs because thermal energy promotes electronic transitions between the metal ion and the ligands. As temperature increases, the ligand field interaction may change slightly, shifting the absorption spectrum and resulting in a more intensely coloured complex.
(ii) Write the electronic configuration for a \(d^5\) ion if \(\Delta_o < P\).
Answer: When \(\Delta_o < P\), the complex forms a high-spin configuration. Thus, the electronic configuration is:
\[ t_{2g}^3 e_g^2 \]
This means three electrons occupy the lower-energy \(t_{2g}\) orbitals and two occupy the higher-energy \(e_g\) orbitals, following Hund’s rule of maximum multiplicity.
(iii) Write the hybridization and magnetic behaviour of the complex \([ \text{Ni(CO)}_4 ]\).
(Atomic number: Ni = 28)
Answer: In \([ \text{Ni(CO)}_4 ]\), nickel is in the zero oxidation state. The electron configuration of Ni is:
\[ [\text{Ar}]\, 3d^8 4s^2 \]
CO is a strong field ligand, so it causes pairing of the \(3d\) electrons. All electrons pair up, and the \(4s\) and \(4p\) orbitals hybridize to form four equivalent \(sp^3\) orbitals, giving:
Werner’s coordination theory in 1893 was the first attempt to explain the bonding in coordination complexes. It must be remembered that this theory was put forward before the electron had been discovered by J.J. Thomson in 1897, and before the electronic theory of valency. Werner did not have any of the modern instrumental techniques and all his studies were made using simple experimental techniques. Werner was able to explain the nature of bonding in complexes and he concluded that in complexes, the metal shows two different sorts of valency: primary and secondary. Primary valences are normally ionisable whereas secondary valences are non-ionisable.
Time (Hours) | [A] (M) |
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0 | 0.40 |
1 | 0.20 |
2 | 0.10 |
3 | 0.05 |