Advertisements
Advertisements
Question
The decomposition of A into product has value of k as 4.5 × 103 s−1 at 10°C and energy of activation 60 kJ mol−1. At what temperature would k be 1.5 × 104 s−1?
Advertisements
Solution
Given: k1 = 4.5 × 103 s−1
T1 = 273 + 10 = 283 K
k2 = 1.5 × 104 s−1
Ea = 60 kJ mol−1 = 6.0 × 104 J mol−1
T2 = ?
From Arrhenius equation, we obtain,
`log k_2/k_1 = E_a/(2.303 R)((T_2 - T_1)/(T_1T_2))`
⇒ log `(1.5 xx 10^4)/(4.5 xx 10^3) = (60000)/(2.303 xx 8.314) ((T_2 - 283) /(283 xx T_2))`
⇒ log 3.333 = `3133.63 (T_2 - 283)/(283 xx T_2)`
⇒ 0.5228 = `3133.63 (T_2 - 283)/(283 xx T_2)`
⇒ `0.5228/3133.63 = (T_2 - 283)/(283 xx T_2)`
⇒ 1.6683 × 10−4 = `(T_2 - 283)/(283 xx T_2)`
⇒ 1.6683 × 10−4 × 283 × T2 = T2 − 283
⇒ 0.0472 T2 = T2 − 283
283 = T2 − 0.0472 T2
283 = (1 − 0.0472) T2
283 = 0.9528 T2
⇒ T2 = `283/0.9528`
= 297 K
= 297 − 273
= 24°C
Hence, k would be 1.5 × 104 s−1 at 24°C.
Notes
The answer in the textbook is incorrect.
RELATED QUESTIONS
What will be the effect of temperature on rate constant?
The rate constant for the decomposition of N2O5 at various temperatures is given below:
| T/°C | 0 | 20 | 40 | 60 | 80 |
| 105 × k/s−1 | 0.0787 | 1.70 | 25.7 | 178 | 2140 |
Draw a graph between ln k and `1/T` and calculate the values of A and Ea. Predict the rate constant at 30º and 50ºC.
The rate of a reaction quadruples when the temperature changes from 293 K to 313 K. Calculate the energy of activation of the reaction assuming that it does not change with temperature.
Calculate activation energy for a reaction of which rate constant becomes four times when temperature changes from 30 °C to 50 °C. (Given R = 8.314 JK−1 mol−1).
Predict the main product of the following reactions:
The reaction between \[\ce{H2(g)}\] and \[\ce{O2(g)}\] is highly feasible yet allowing the gases to stand at room temperature in the same vessel does not lead to the formation of water. Explain.
Why does the rate of a reaction increase with rise in temperature?
Match the statements given in Column I and Column II
| Column I | Column I | |
| (i) | Catalyst alters the rate of reaction | (a) cannot be fraction or zero |
| (ii) | Molecularity | (b) proper orientation is not there always |
| (iii) | Second half life of first order reaction | (c) by lowering the activation energy |
| (iv) | `e^((-E_a)/(RT)` | (d) is same as the first |
| (v) | Energetically favourable reactions (e) total probability is one are sometimes slow | (e) total probability is one |
| (vi) | Area under the Maxwell Boltzman curve is constant | (f) refers to the fraction of molecules with energy equal to or greater than activation energy |
Total number of vibrational degrees of freedom present in CO2 molecule is
For an endothermic reaction energy of activation is Ea and enthalpy of reaction ΔH (both of there in KJ moI–1) minimum value of Ea will be ______.
The activation energy in a chemical reaction is defined as ______.
The activation energy in a chemical reaction is defined as ______.
Arrhenius equation can be represented graphically as follows:

The (i) intercept and (ii) slope of the graph are:
Explain how and why will the rate of reaction for a given reaction be affected when the temperature at which the reaction was taking place is decreased.
The equation k = `(6.5 xx 10^12 "s"^(-1))"e"^(- 26000 " K"//"T")` is followed for the decomposition of compound A. The activation energy for the reaction is ______ kJ mol-1. (Nearest integer) (Given: R = 8.314 JK-1 mol-1)
An exothermic reaction X → Y has an activation energy 30 kJ mol-1. If energy change ΔE during the reaction is - 20 kJ, then the activation energy for the reverse reaction in kJ is ______.
It is generally observed that the rate of a chemical reaction becomes double with every 10°C rise in temperature. If the generalisation holds true for a reaction in the temperature range of 298 K to 308 K, what would be the value of activation energy (Ea) for the reaction?
