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Question #44584
The Question
A researcher is investigating a diamagnetic, binuclear complex of Iron (Fe) containing terminal carbonyl (CO) and bridging nitrosyl (NO) ligands, with the general formula . The NO ligands act as 3-electron donors to the dimer.
Initially, the researcher predicts the stoichiometry by assuming the complex strictly obeys the 18-electron (EAN) rule with NO metal-metal bonds, while maintaining an octahedral geometry ( hybridization) around each Iron atom.
However, X-ray crystallography reveals the actual complex has the stoichiometry , maintains the hybridization, but contains exactly ONE Fe-Fe single bond.
What are the values of the predicted stoichiometry and the actual stoichiometry , respectively?
Options
- A.
and
- B.
and
- C.
and
- D.
and
Check Your Answer
Correct Answer
Step-by-Step Solution
Explanation
How the Examiner Thinks
Numerical_Precision
Improve calculation stamina and avoid rounding errors in high-stakes competitive examinations.
Concepts Behind This Question
Valence Bond Theory Hybridization|EAN Rule (Sidgwick's Rule)|Coordination Compounds - Class 12
Why This Question Is Tricky
Common Mistakes
This problem tests the intersection of the Effective Atomic Number (EAN) rule and Valence Bond Theory (VBT) in multi-nuclear organometallic complexes.
The core trap is the dual role of a metal-metal bond: students often remember that it reduces the required Total Valence Electrons (TVE) by 2, but they frequently forget that it also occupies a physical coordination site (a hybrid orbital) in VBT.
Failing to account for the M-M bond in the Coordination Number calculation leads to incorrect stoichiometric predictions.
Additionally, it tests the knowledge of bridging NO as a 3-electron donor, distinguishing it from standard 2-electron donors.
Quick Facts About This Question
Question Information
| Subject | Chemistry |
| Chapter | Coordination Compounds - Class 12 |
| Concept | Valence Bond Theory Hybridization |
| Difficulty | 8 |
| Cognitive Load | 7 |
| Target Solve Time | 160 sec |
| Access | Free |