Crystal Field Theory (CFT) explains the splitting of metal d-orbitals based on ligand interactions. The strength of a ligand, often referred to as its position in the spectrochemical series, determines the magnitude of the crystal field splitting ($\Delta_o$). Strong field ligands cause a larger splitting compared to weak field ligands.
Ligands are ranked according to their field strength. For the given ligands:
The correct order reflecting the decreasing field strength of these ligands, according to the spectrochemical series, is:
CO > NH3 > H2O > Cl-
Match List I with List II :
| List I (Transition metal/compound) | List II (Catalytic Role) |
| A. $V_2O_5$ | I. Preparation of ammonia from $N_2/H_2$ mixture |
| B. Fe | II. Polymerisation of alkynes |
| C. $PdCl_2$ | III. Preparation of $H_2SO_4$ from $SO_2$ |
| D. Ni complex | IV. Oxidation of ethyne to ethanal |
Choose the correct answer :
Match List I with List II :
| List I (Complex/Ion) | List II (Shape/geometry) |
| A. $[Pt(Cl)_2(NH_3)_2]$ | I. Octahedral |
| B. $[Co(NH_3)_6]Cl_3$ | II. Trigonal bipyramidal |
| C. $[NiCl_4]^{2-}$ | III. Square planar |
| D. $[Fe(CO)_5]$ | IV. Tetrahedral |
Choose the correct answer :
Match List I with List II :
| List I (Complex) | List II (Type of Isomerism) |
| A. $[Pt(NH_3)_2Cl_2]$ | I. Optical |
| B. $[Co(en)_3]^{3+}$ | II. Solvate |
| C. $[Co(NH_3)_4(NO_2)_2]Cl$ | III. Geometrical |
| D. $[Cr(H_2O)_6]Cl_3$ | IV. Linkage |
Choose the correct answer :
| List I | List II |
|---|---|
| A. $PCl_5$ | I. Tetrahedral |
| B. $BrF_5$ | II. Square Planar |
| C. $BF_4^-$ | III. Trigonal bipyramidal |
| D. $[Ni(CN)_4]^{2-}$ | IV. Square pyramidal |
The crystal field splitting energy of $[\text{Co(oxalate)}_3]^{3-}$ complex is '$n$' times that of the $[\text{Cr(oxalate)}_3]^{3-}$ complex. Here '$n$' is ___________. (Assume $\Delta_o >> P$)