Question:

Among the following metal carbonyl species, the one with the highest metal-carbon back bonding is

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Back bonding is most effective when the metal has a low oxidation state and the ligand (CO) can accept electron density into its \( \pi^* \) orbitals.
Updated On: Dec 14, 2025
  • \([ \text{Ti(CO)}_6 ]^{2-} \)
  • \([ \text{V(CO)}_6 ]^{-} \)
  • \([ \text{Cr(CO)}_6 ] \)
  • \([ \text{Mn(CO)}_6 ]^{+} \)
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The Correct Option is A

Solution and Explanation

Understanding metal-carbon back bonding in metal carbonyls:

Back bonding occurs when:

  1. Metal donates electron density from filled d-orbitals
  2. Into empty π* antibonding orbitals of CO
  3. This strengthens M-C bond and weakens C-O bond

Factors favoring strong back bonding:

  • High electron density on metal (negative charge, low oxidation state)
  • Good orbital overlap between metal d-orbitals and CO π* orbitals

Analyzing each complex:

(A) [Ti(CO)₆]²⁻

  • Ti in oxidation state: -2 (very electron-rich)
  • Configuration: Ti²⁻ has d⁶ configuration
  • Very high electron density on metal
  • Strong back donation expected
  • Highest back bonding 

(B) [V(CO)₆]⁻

  • V in oxidation state: -1
  • Configuration: V⁻ has d⁶ configuration
  • High electron density, but less than Ti²⁻
  • Strong back bonding, but less than (A)

(C) Cr(CO)₆

  • Cr in oxidation state: 0
  • Configuration: Cr⁰ has d⁶ configuration
  • Neutral metal, moderate electron density
  • Good back bonding, but less than charged species

(D) [Mn(CO)₆]⁺

  • Mn in oxidation state: +1
  • Configuration: Mn⁺ has d⁶ configuration
  • Positive charge reduces electron density
  • Weakest back bonding among these

Trend: As metal becomes more electron-rich (more negative charge), back bonding increases.

Order: [Ti(CO)₆]²⁻ > [V(CO)₆]⁻ > Cr(CO)₆ > [Mn(CO)₆]⁺

Answer: (A) [Ti(CO)₆]²⁻

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