Match the LIST-I with LIST-II.
| LIST-I (Coordination Complex) | LIST-II (Characteristic) | ||
| A. | [Co(NH3)6]Cl3 | I. | Square Planar |
| B. | [Ni(CO)4] | II. | t2g4eg2 |
| C. | [CoF6]Br3 | III. | Tetrahedral |
| D. | [Ni(CN)4]Cl2 | IV. | t2g6 |
Choose the correct answer from the options given below:
Answer & explanation
Correct answer: option 3
The correct answer is Option (3) → A-IV, B-III, C-II, D-I
The d electron count of the metal ion and the strength of the ligand field decide the arrangement of electrons and the shape of a complex. In an octahedral field, the d orbitals split into t2g (lower) and eg (higher). A strong field ligand (\( \ce{CN^{-}} \), CO, \( \ce{NH3} \) with \( \ce{Co^{3+}} \)) makes the splitting larger than the pairing energy, so the electrons pair up in t2g. A weak field ligand (\( \ce{F^{-}} \)) gives a small splitting, so the electrons occupy eg before pairing.
(A) \( \ce{[Co(NH3)6]Cl3} \) — This matches (IV) t2g6. \( \ce{NH3} \) is neutral and three \( \ce{Cl^{-}} \) ions are outside the bracket, so cobalt is +3. Co (Z = 27) is [Ar]3d74s2; losing the two 4s electrons and one 3d electron leaves 3d6, and \( \ce{NH3} \) acts as a strong field ligand with \( \ce{Co^{3+}} \), so all six electrons pair in t2g (low spin, d2sp3, diamagnetic).
(B) \( \ce{[Ni(CO)4]} \) — This matches (III) Tetrahedral. CO is neutral, so nickel is in the zero oxidation state: Ni (Z = 28) is [Ar]3d84s2. CO is a strong field ligand, so the 4s electrons pair into 3d, giving 3d10. The empty 4s and 4p orbitals give sp3 hybridisation, and the complex is tetrahedral and diamagnetic.
(C) \( \ce{[CoF6]Br3} \) — This matches (II) t2g4eg2. The complex ion \( \ce{[CoF6]^{3-}} \) has cobalt in the +3 state (x + 6(−1) = −3), so it is Co3+, 3d6 as worked out in (A); as printed, [CoF6]Br3 would need cobalt in the +9 state, so the item is read as the complex ion, and \( \ce{F^{-}} \) is a weak field ligand. The electrons go into eg before pairing, giving the high spin arrangement t2g4eg2 with four unpaired electrons (sp3d2, paramagnetic).
(D) \( \ce{[Ni(CN)4]Cl2} \) — This matches (I) Square Planar. The complex ion \( \ce{[Ni(CN)4]^{2-}} \) has nickel in the +2 state (x + 4(−1) = −2); losing the two 4s electrons of Ni ([Ar]3d84s2) gives Ni2+, 3d8 (as printed, [Ni(CN)4]Cl2 would need nickel in the +6 state). The strong field \( \ce{CN^{-}} \) ligands pair the two unpaired electrons, leaving one 3d orbital empty. This gives dsp2 hybridisation, so the complex is square planar and diamagnetic.
Shortcut: The pair A–IV appears in Options (3) and (4), and B–III then leaves only Option (3).
Note: It seems that there is a mistake in the original NTA paper, which prints [CoF6]Br3 (item C) and [Ni(CN)4]Cl2 (item D) when it should read K3[CoF6] and K2[Ni(CN)4].