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Chemistry · CHEMICAL BONDING AND MOLECULAR STRUCTURE

हिन्दी

In the resonance structures of ozone (\( \text{O}_3 \)) shown in Fig. 4.3 on the page, canonical forms I and II have distinct single and double bonds, while structure III represents the resonance hybrid. Which of the following statements correctly explains why structure III has identical \( \text{O}-\text{O} \) bond lengths of \( 128\text{ pm} \)?

Question diagram
  1. A
    The actual structure fluctuates rapidly between canonical forms I and II in a rapid dynamic equilibrium.
  2. B
    The two oxygen-oxygen bonds differ in energy, but spatial symmetry forces their physical bond lengths to appear identical.
  3. C
    The ozone molecule spends \( 50\% \) of its time as structure I and \( 50\% \) of its time as structure II.
  4. D
    Both canonical forms have no independent existence; the resonance hybrid represents the intermediate bond character with delocalised electron density.
View Answer & Solution

Correct answer · Option D

Both canonical forms have no independent existence; the resonance hybrid represents the intermediate bond character with delocalised electron density.

Explanation

Canonical structures have no real existence. The resonance hybrid III is a single stable structure where electron delocalisation renders both O-O bonds equivalent and intermediate (128 pm).
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