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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.
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The rate constants for the decomposition of N2O5 at different temperatures are shown below.
| T(°C) | T(K) | 1/T | k(s−1) | In k (= 2.303 log k) |
| 0 | 273 | 3.6 × 10−3 | 7.87 × 10−7 | −14.06 |
| 20 | 293 | 3.4 × 10−3 | 1.70 × 10−5 | −10.98 |
| 40 | 313 | 3.19 × 10−3 | 25.7 × 10−5 | −8.266 |
| 60 | 333 | 3.00 × 10−3 | 178 × 10−5 | −6.332 |
| 80 | 353 | 2.8 × 10−3 | 2140 × 10−5 | −3.844 |

Slope of the line = tan θ
= `(y_2 - y_1)/(x_2 - x_1)`
= `(-10.98 - (-14.06))/(3.4 - 3.6) xx 10^3`
= `3.08/-0.2 xx 10^3`
= −15.4 × 103
Ea = −slope × R
= −(−15.4 × 103 × 8.314)
= 128.035 kJ K−1 mol−1
Again In A = In k + `E_a/(RT)`
= `-14.06 + (128.035 xx 10^3)/(8.314 xx 273)`
= `-14.06 + 128035/2269.722`
= −14.06 + 56.40
= 42.34
or, log A = 42.34
or, A = antilog 42.34 = 0.3388 × 1019
or, A = 3.3888 × 1018
Values of rate constant k at 303 K and 323 K can be obtained from the graph.
First, k is obtained corresponding to `1/(303 K) and 1/(323 K)` and then k is calculated.
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Explain a graphical method to determine activation energy of a reaction.
Consider the reaction
`3I_((aq))^-) +S_2O_8^(2-)->I_(3(aq))^-) + 2S_2O_4^(2-)`
At particular time t, `(d[SO_4^(2-)])/dt=2.2xx10^(-2)"M/s"`
What are the values of the following at the same time?
a. `-(d[I^-])/dt`
b. `-(d[S_2O_8^(2-)])/dt`
c. `-(d[I_3^-])/dt`
The rate constant of a first order reaction increases from 2 × 10−2 to 4 × 10−2 when the temperature changes from 300 K to 310 K. Calculate the energy of activation (Ea).
(log 2 = 0.301, log 3 = 0.4771, log 4 = 0.6021)
What will be the effect of temperature on rate constant?
The rate of the chemical reaction doubles for an increase of 10 K in absolute temperature from 298 K. Calculate Ea.
The decomposition of hydrocarbon follows the equation k = `(4.5 xx 10^11 s^-1) e^(-28000 K//T)`
Calculate Ea.
In the Arrhenius equation for a first order reaction, the values of ‘A’ of ‘Ea’ are 4 × 1013 sec−1 and 98.6 kJ mol−1 respectively. At what temperature will its half life period be 10 minutes?
[R = 8.314 J K−1 mol−1]
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 chemical reaction in which reactants require high amount of activation energy are generally ____________.
During decomposition of an activated complex:
(i) energy is always released
(ii) energy is always absorbed
(iii) energy does not change
(iv) reactants may be formed
Which of the following statements are in accordance with the Arrhenius equation?
(i) Rate of a reaction increases with increase in temperature.
(ii) Rate of a reaction increases with decrease in activation energy.
(iii) Rate constant decreases exponentially with increase in temperature.
(iv) Rate of reaction decreases with decrease in activation energy.
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
The rate constant for a reaction is 1.5 × 10–7 sec–1 at 50°C. What is the value of activation energy?
The activation energy in a chemical reaction is defined as ______.
The slope of Arrhenius Plot `("In" "k" "v"//"s" 1/"T")` of first-order reaction is −5 × 103 K. The value of Ea of the reaction is. Choose the correct option for your answer. [Given R = 8.314 JK−1mol−1]
The decomposition of N2O into N2 and O2 in the presence of gaseous argon follows second-order kinetics, with k = (5.0 × 1011 L mol−1 s−1) `"e"^(-(29000 "K")/"T")`. Arrhenius parameters are ______ kJ 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 ______.
