Before You Begin
Question #44850
The Question
A rigid reactor of volume contains a solid tungsten catalyst with a total active surface area of . The decomposition of \ce{NH3(g)} on the catalyst surface at and an initial pressure of follows zero-order kinetics due to complete surface saturation (Langmuir-Hinshelwood mechanism).
The catalyst surface has a site density of . The rate-determining step is the decomposition of adsorbed \ce{NH3}, which occurs with a transition state vibrational frequency of .
Given the activation energy for the surface reaction is , calculate the magnitude of the initial rate of change of the partial pressure of \ce{NH3(g)} in the reactor.
(Assume ideal gas behavior, , , and . Each active site decomposes one \ce{NH3} molecule per effective vibration.)
Options
- A.
- B.
- C.
- D.
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
Units of Rate Constant (k)|Collision Frequency vs. Effective Collisions|Zero Order Rate Integration
Why This Question Is Tricky
Common Mistakes
The problem tests the 'Hidden Variable' of dimensionality in heterogeneous catalysis.
Students often memorize the Arrhenius equation and zero-order kinetics in terms of volumetric concentration ().
Here, the 'effective collision' frequency is limited by the 2D surface site saturation, meaning the pre-exponential factor and rate constant must be defined per unit area ().
Failing to account for the catalyst's surface area or incorrectly treating as a volumetric parameter leads to massive dimensional and numerical errors (as seen in the distractors).
Quick Facts About This Question
Question Information
| Subject | Chemistry |
| Chapter | Chemical Kinetics - Class 12 |
| Concept | Units of Rate Constant (k) |
| Difficulty | 8 |
| Cognitive Load | 7 |
| Target Solve Time | 160 sec |
| Access | Free |