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Question #44145

Difficulty: 8/10 | 🟢 Free

The Question

Consider the central atoms in the following species: (I) \ce{CrO5} (II) \ce{H2SO5} (III) \ce{XeF6} (IV) \ce{ClO2}

Which of the following statements correctly describes the ability of the central atom in these species to undergo disproportionation (for III, specifically into other binary fluorides) under standard conditions, and identifies the underlying structural reasons?

Options

  • A.

    The central atoms in (I) and (II) cannot disproportionate as they are already in their maximum +6 oxidation states due to peroxy linkages; (III) disproportionates into \ce{XeF4} and \ce{XeF8} because Xe can expand its octet to +8.

  • B.

    The central atoms in (I), (II), and (III) cannot disproportionate; (I) and (II) are at their maximum +6 oxidation state due to peroxy linkages, and (III) cannot form the sterically and thermodynamically unstable \ce{XeF8}. The central atom in (IV) disproportionates in an alkaline medium.

  • C.

    The central atoms in (I) and (II) undergo disproportionation because their formal oxidation states (+10 and +8) are highly unstable; (IV) cannot disproportionate as Cl is in a stable +4 state.

  • D.

    The central atoms in (II) and (IV) disproportionate to yield S(+8)/S(+4) and Cl(+5)/Cl(+3) respectively, while (I) and (III) cannot disproportionate due to the absence of higher accessible oxidation states for Cr and Xe.

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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

Disproportionation Constraints|Stability of High O.S. Fluorides/Oxides|Peroxy Linkage Identification

Why This Question Is Tricky

Common Mistakes

This question evaluates the student's ability to differentiate between algebraically calculated formal oxidation states and actual structural oxidation states.

A common pedagogical trap is blindly applying the algebraic sum rule, leading to impossible oxidation states (e.g., +10 for Cr in \ce{CrO5} or +8 for S in \ce{H2SO5}).

Recognizing the peroxy linkages reveals the central atoms are already at their maximum group oxidation states (+6), making disproportionation impossible.

Furthermore, the question tests the 'Stability of High O.S.

Fluorides' exception: while Xe can reach a +8 oxidation state with oxygen, \ce{XeF8} is sterically forbidden.

This prevents the disproportionation of \ce{XeF6} into binary fluorides, acting as a secondary trap for students who only consider electronic configurations without steric constraints.

Quick Facts About This Question

Question Information

SubjectChemistry
ChapterRedox Reactions - Class 11 Part 2
ConceptDisproportionation Constraints
Difficulty8
Cognitive Load7
Target Solve Time160 sec
AccessFree
Redox Reactions - Class 11 Part 2 Practice Question 44145 | RankRise360