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Question #44159

Difficulty: 8/10 | 🟢 Free

The Question

Consider the gaseous transition metal dimer \ceCr2\ce{Cr2}. Assuming ideal Molecular Orbital Theory (MOT) for d-block dimers where all valence electrons participate in bonding, determine the formal bond order, its magnetic nature, and the number of δ\delta-bonds present in its ground state.

Options

  • A.

    6, \text{Diamagnetic}, 2

  • B.

    5, \text{Paramagnetic}, 1

  • C.

    4, \text{Diamagnetic}, 0

  • D.

    0, \text{Paramagnetic}, 0

Check Your Answer

Correct Answer

Step-by-Step Solution

Explanation

How the Examiner Thinks

Exception_Exposure

Learn to identify edge cases and boundary exceptions that JEE examiners hide in math problems.

Concepts Behind This Question

MOT and Magnetic Nature|Aufbau Principle Exceptions|Screening Effect in Inner Shells

Why This Question Is Tricky

Common Mistakes

This question tests the limits of Molecular Orbital Theory (MOT) by moving beyond the standard s−ps-p mixing seen in period 2 homonuclear diatomics (like \ceO2\ce{O2} or \ceN2\ce{N2}).

Students often incorrectly assume that dd-electrons remain non-bonding or that the 3d54s13d^5 4s^1 configuration will lead to a highly paramagnetic species due to Hund's rule in isolated atoms.

The hidden mechanism here is the profound inner-shell dd-orbital overlap that occurs in Group 6 dimers, leading to the formation of a sextuple bond (comprising σ\sigma, π\pi, and δ\delta interactions) and a completely diamagnetic ground state.

Failing to account for δ\delta-bond formation from face-to-face dd-orbital overlap is a critical trap.

Quick Facts About This Question

Question Information

SubjectChemistry
ChapterChemical Bonding and Molecular Structure - Class 11 Part 1
ConceptMOT and Magnetic Nature
Difficulty8
Cognitive Load7
Target Solve Time160 sec
AccessFree