Give the oxidation state, d-orbital occupation and coordination number of the central metal ion in the following complexes:
(i) \(K_3[Co(C_2O_4)_3] \)
(ii)\( cis-[Cr(en)_2Cl_2]Cl \)
(iii) \((NH_4)_2[CoF_4] \)
(iv) \([Mn(H_2O)_6]SO_4\)
(i) \(K_3[Co(C_2O_4)_3] \)
The central metal ion is \(Co.\)
Its coordination number is \(6\).
The oxidation state can be given as:
\(x-6 =-3 \)
\(x =+3 \)
The d orbital occupation for\( Co^{ 3+}\) is \(t_{2g}^{ 6}e_g^{0}.\)
(ii) \(cis-[Cr(en)_2Cl_2]Cl \)
The central metal ion is \(Cr. \)
The coordination number is \(6.\)
The oxidation state can be given as:
\(x+2(0)+2(-1)=+1 \)
\(x - 2 = +1\)
\(x = +3 \)
The d orbital occupation for \(Cr^{3+}\) is \(t_{2g}^{3} .\)
(iii) \((NH_4)_2[CoF_4]\) The central metal ion is\( Co. \)
The coordination number is \(4. \)
The oxidation state can be given as:
\(x-4 =-2 \)
\(x=+2\) The d orbital occupation for \(Co^{2+} \)is \(e_g^{4}\space t_{2g} ^{3}.\)
(iv) \([Mn(H_2O)_6]SO_4 \)The central metal ion is \(Mn.\)
The coordination number is \(6\).
The oxidation state can be given as:
\(x+0=+2 \)
\(x=+2\) The d orbital occupation for \(Mn \) is \(t_{2g}^{3}\space e_g^{2} .\)
The correct IUPAC name of \([ \text{Pt}(\text{NH}_3)_2\text{Cl}_2 ]^{2+} \) is:
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
What is crystal field splitting energy?
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
On the basis of CFT, explain why [Ti(H$_2$O)$_6$]Cl$_3$ complex is coloured? What happens on heating the complex [Ti(H$_2$O)$_6$]Cl$_3$? Give reason.

A ladder of fixed length \( h \) is to be placed along the wall such that it is free to move along the height of the wall.
Based upon the above information, answer the following questions:
(iii) (b) If the foot of the ladder, whose length is 5 m, is being pulled towards the wall such that the rate of decrease of distance \( y \) is \( 2 \, \text{m/s} \), then at what rate is the height on the wall \( x \) increasing when the foot of the ladder is 3 m away from the wall?
The metal-carbon bond possesses both the σ and π character in a metal carbonyl. The synergic effect produced by the metal-ligand bond strengthens the bond between the carbonyl molecule and the metal. The types of bonding that exist in metal carbonyls are as follows:
They are found to dissociate in various solutions. The stability of a coordination compound in a solution mainly depends on the degree of association between the two species involved in the state of equilibrium. For the formation of the compound quantitatively the stability of any complex is given by the magnitude of the equilibrium constant. For instance,
A + 4B→ AB4