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Question #44831

Difficulty: 8/10 | 🟢 Free

The Question

The diazotization of aniline (\ceC6H5NH2\ce{C6H5NH2}) with \ceNaNO2\ce{NaNO2} and aqueous \ceHCl\ce{HCl} is optimally carried out at 278 K278\text{ K}, where the stable benzenediazonium chloride accumulates at a rate r1r_1. A student attempts to optimize the process by raising the reaction temperature to 298 K298\text{ K}. Assuming a temperature coefficient μ=2\mu = 2 for the reaction kinetics, the student predicts a new accumulation rate rpredictedr_{predicted} for the diazonium salt. However, experimentally, the actual accumulation rate of the diazonium salt at 298 K298\text{ K} is found to be ractualr_{actual}, accompanied by the vigorous evolution of a colorless gas and the formation of a major organic product P\textbf{P}.

Which of the following correctly identifies rpredictedr_{predicted}, ractualr_{actual}, and the product P\textbf{P}?

Options

  • A.

    rpredicted=4r1r_{predicted} = 4r_1; ractual≈0r_{actual} \approx 0; P=Phenol\textbf{P} = \text{Phenol}

  • B.

    rpredicted=2r1r_{predicted} = 2r_1; ractual=2r1r_{actual} = 2r_1; P=Chlorobenzene\textbf{P} = \text{Chlorobenzene}

  • C.

    rpredicted=4r1r_{predicted} = 4r_1; ractual=4r1r_{actual} = 4r_1; P=Benzenediazonium chloride\textbf{P} = \text{Benzenediazonium chloride}

  • D.

    rpredicted=4r1r_{predicted} = 4r_1; ractual≈0r_{actual} \approx 0; P=p-Aminoazobenzene\textbf{P} = p\text{-Aminoazobenzene}

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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

Temperature Coefficient (Q10)|Diazotization Temperature Sensitivity

Why This Question Is Tricky

Common Mistakes

This question tests the 'Lethal Collision' trap, where students blindly apply mathematical kinetic models (like the Q10Q_{10} temperature coefficient) without accounting for the thermal instability of the reaction intermediate.

While the Arrhenius equation predicts a four-fold increase in the reaction rate, the arenediazonium salt degrades rapidly above 5∘C5^\circ\text{C} (278 K278\text{ K}).

This creates a kinetic cliff where the effective yield and accumulation rate of the desired product drop to zero, overriding the theoretical kinetic extrapolation.

It also tests the competing pathways at higher temperatures, where hydrolysis to phenol dominates over diazo coupling in strongly acidic media.

Quick Facts About This Question

Question Information

SubjectChemistry
ChapterChemical Kinetics - Class 12
ConceptTemperature Coefficient (Q10)
Difficulty8
Cognitive Load7
Target Solve Time160 sec
AccessFree