Q.22 Match the coordination complexes given in Column I with the most appropriate properties in Column II.
(Given: Atomic numbers of Mn: 25; Co: 27; Ni: 28)
| Column I Coordination complexes |
Column II Properties |
|---|---|
| E. [Mn(H2O)6]2+ F. [CoF6]3− G. [NiCl4]2− H. [Ni(CN)4]2− |
1. 5.92 Bohr Magneton (BM) 2. CFSE = 0.4 Δo 3. Metal ion hybridisation is sp3 4. Diamagnetic |
(A) E–1, F–2, G–3, H–4
(B) E–2, F–1, G–4, H–3
(C) E–4, F–2, G–1, H–3
(D) E–1, F–4, G–3, H–2
Introduction
This article explains how to match the coordination complexes [Mn(H₂O)₆]²⁺, [CoF₆]³⁻, [NiCl₄]²⁻ and [Ni(CN)₄]²⁻ with the most appropriate properties using crystal field theory, hybridisation and spin-only magnetic moments.[web:23][web:26][web:9][web:18] The discussion is designed for competitive exams, especially where understanding of high-spin and low-spin complexes is essential.
Data from the question
Column I: Coordination complexes
- E. [Mn(H₂O)₆]²⁺
- F. [CoF₆]³⁻
- G. [NiCl₄]²⁻
- H. [Ni(CN)₄]²⁻
Column II: Properties
- 5.92 Bohr Magneton (BM)
- CFSE = 0.4 Δ₀
- Metal ion hybridisation is sp³
- Diamagnetic
Detailed analysis of each complex
E. [Mn(H₂O)₆]²⁺
Mn has atomic number 25, so Mn²⁺ has configuration 3d⁵ and with weak field H₂O ligands it forms a high-spin octahedral complex with five unpaired electrons.
The spin‑only magnetic moment is given by the formula
μ = √n(n + 2) with n = 5 gives μ = √35 ≈ 5.92 BM.
Therefore, [Mn(H₂O)₆]²⁺ corresponds to property 1 (5.92 BM) → E–1.
F. [CoF₆]³⁻
- In [CoF₆]³⁻ the oxidation state of Co is +3; Co³⁺ is 3d⁶.
- F⁻ is a weak field ligand, so the complex is octahedral, high‑spin, with configuration t₂g4eg2, giving four unpaired electrons.
- For d⁶ high‑spin octahedral: CFSE = −0.4 × 4Δo + 0.6 × 2Δo = −1.6Δo + 1.2Δo = −0.4Δo, so magnitude 0.4 Δo as given in Column II.
Thus [CoF₆]³⁻ corresponds to property 2 (CFSE = 0.4 Δo) → F–2.
G. [NiCl₄]²⁻
Nickel has atomic number 28, so Ni²⁺ is 3d⁸ in both [NiCl₄]²⁻ and [Ni(CN)₄]²⁻. Chloride is a weak field ligand, so no pairing occurs and the complex adopts tetrahedral geometry with sp³ hybridisation using the 4s and 4p orbitals, containing two unpaired electrons and therefore paramagnetic.
Hence [NiCl₄]²⁻ matches property 3 (metal ion hybridisation is sp³) → G–3.
H. [Ni(CN)₄]²⁻
In [Ni(CN)₄]²⁻ the metal is again Ni²⁺ (3d⁸), but CN⁻ is a strong field ligand that causes pairing of the 3d electrons. This leads to dsp² hybridisation and a square‑planar low‑spin complex in which all d‑electrons are paired, making the complex diamagnetic.
Therefore [Ni(CN)₄]²⁻ corresponds to property 4 (diamagnetic) → H–4.
Checking the options (A–D)
| Option | E ([Mn(H₂O)₆]²⁺) | F ([CoF₆]³⁻) | G ([NiCl₄]²⁻) | H ([Ni(CN)₄]²⁻) | Correct or not |
|---|---|---|---|---|---|
| (A) | 1 | 2 | 3 | 4 | All correct |
| (B) | 2 | 1 | 4 | 3 | All wrong |
| (C) | 4 | 2 | 1 | 3 | All wrong |
| (D) | 1 | 4 | 3 | 2 | F and H wrong |
Since only option (A) reproduces the correct set E–1, F–2, G–3, H–4, the answer is (A).


