Chemical Kinetics Mock Test – Class 12 Chemistry
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Chemical Kinetics Mock Test – Class 12 Chemistry

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Chemical Kinetics – Progressive Test

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1. A catalyst lowers the activation energy from to . Assuming the same pre-exponential factor, the ratio at is closest to:

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2. An energy profile has and . The reverse activation energy is:

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3. A mechanism contains a fast step followed by the slow elementary step . Why is not usually accepted as the final overall rate law?

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4. In the rate law , the rate constant is:

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5. The table lists values of for the same reaction at three temperatures.

Temperature condition
P
Q
R

Assuming the same , the order of rate constants is:

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6. A proposed mechanism is:


Writing as the final experimentally usable rate law is incomplete because:

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7. Assertion: The slope of an Arrhenius plot of against is negative, although activation energy is positive.
Reason: The slope is equal to .

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8. Reaction order is assessed through the statements below.
Statement I: An overall order may be zero.
Statement II: An overall order may be fractional.
Statement III: Every overall reaction must have a positive whole-number order.
The valid statements are:

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9. Assertion: The average rate of disappearance of a reactant is conventionally reported as a positive quantity.
Reason: During forward reaction progress, the concentration change of a consumed reactant is negative.

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10. A linear zero-order concentration-time graph has vertical intercept and slope . The extrapolated time-axis intercept is:

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11. Match each quantity in Column I with its usual unit or symbol in Column II.

Column I Column II
P. Concentration 1.
Q. Time 2.
R. Absolute temperature 3.
S. Reaction rate 4.

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12. According to collision theory, a chemical reaction can occur when reactant particles:

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13. Reaction rate is quantitatively described as:

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14. Which description best represents a graph of against absolute temperature for an ordinary reaction with positive activation energy?

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15. A zero-order reaction and a first-order reaction begin with the same reactant concentration and the same initial rate. At a later time, both reactions are still proceeding and the zero-order reaction remains within its valid kinetic regime. Their rates are then best compared by stating that:

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16. For zero-order disappearance, and . The concentration after is:

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17. A concentration-time line for zero-order disappearance has slope and vertical intercept . Its half-life and idealised completion time are:

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18. When the temperature of a reacting system is raised while concentrations and other conditions are kept unchanged, the reaction rate generally:

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19. During an interval, a reactant concentration decreases from to . Its average rate of disappearance is:

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20. The following average disappearance rates were obtained for successive intervals of the same reaction.

Interval Average disappearance rate
P.
Q.
R.

The data support the conclusion that:

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21. A process has a negative Gibbs energy change under certain conditions but proceeds extremely slowly. This observation shows that:

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22. Which feature may appear on a catalysed energy profile even when the uncatalysed profile has only one peak?

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23. When is held constant for the rate law , the missing exponent in the rate-ratio relation is ______.

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24. The units of rate constants are assessed through the statements below.
Statement I: The time dimension of is always reciprocal time for a rate law written in the usual concentration form.
Statement II: The concentration dimension of depends on the overall reaction order.
Statement III: The unit of reaction rate changes with reaction order.
The valid statements are:

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25. Concentration-time data for a reaction are shown below.

Time

If the reaction is zero order, the graph parameters are:

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26. A student uses

for the reaction , where is the total pressure. The procedure is incorrect because:

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27. Two experiments use identical initial concentrations and the same catalyst condition, but Experiment Q is performed at a higher temperature than Experiment P. If the reaction mechanism remains unchanged, the most likely result is:

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28. Two energy-distribution curves P and Q correspond to the same gas sample at different temperatures. Curve Q has a lower maximum, is broader, and is shifted toward higher energy. Which comparison is correct?

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29. The limiting relation that connects average and instantaneous rate is:

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30. The rate is expressed as . Its unit indicates:

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31. The instantaneous rate of a reaction at time is obtained conceptually by:

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32. For the true rate law , one experiment uses approximately times . Which interpretation is most suitable?

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33. Taking the natural logarithm of the Arrhenius equation

gives:

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34. Match each collision-theory quantity in Column I with its description in Column II.

Column I Column II
P. Collision frequency, 1. Fraction accounting for favourable orientation
Q. 2. Total encounter frequency
R. Steric factor, 3. Energetic fraction of collisions
S. Effective-collision frequency 4. Product of collision, energy, and orientation factors

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35. Four collisions differ in energy and orientation.

Collision Collision energy Orientation
P Favourable
Q Unfavourable
R Favourable
S Unfavourable

Which collision is effective according to collision theory?

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36. An activation energy of is reported for a reaction whose rate constant at an unknown temperature is four times its value at . The unknown temperature is closest to:

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37. At , a reaction has and . Using , the pre-exponential factor is closest to:

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38. A surface reaction is zero order in reactant while the catalyst surface is saturated. When becomes very small, the rate begins to decrease with . This observation shows that:

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39. Which statement best describes reaction order?

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40. A secant and a tangent are drawn on the same curved reactant concentration-time graph. Their kinetic meanings are:

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41. The measurements are made at identical reactant concentrations and otherwise identical conditions.
Rate data for a reaction are shown below.

Temperature Rate

Assuming a constant temperature coefficient over this range, its value is:

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42. The correct two-temperature Arrhenius relation is:

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43. For a first-order gas reaction , the pressure of remaining at time is represented by the blank:

when is the final total pressure.

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44. The missing relation in the definition of the temperature coefficient is ______.

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45. A rate law determined for a reaction at in the absence of a catalyst should be applied directly to another experiment only when:

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46. On a straight-line Arrhenius plot of against , the point corresponding to the higher temperature lies:

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47. A photochemical reaction is zero order in reactant while the absorbed light intensity remains constant. If the absorbed photon flux is doubled without changing other conditions, the rate is expected to:

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48. Two reactions have Arrhenius parameters:

Reaction
P
Q

Which conclusion is most appropriate at a specified temperature?

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49. The reported reaction rate is . The same rate expressed in is:

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50. The half-life of a first-order reaction is independent of the initial reactant concentration because:

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