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

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

  1. 5.92 Bohr Magneton (BM)
  2. CFSE = 0.4 Δ₀
  3. Metal ion hybridisation is sp³
  4. 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).

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