Advertisements
Advertisements
प्रश्न
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]
In the Arrhenius equation for a certain reaction, the value of A and Ea (activation energy) are 4 × 1013 sec−1 and 98.6 kJ mol−1 respectively. If the reaction is of first order, at what temperature will its half-life period be ten minutes?
Advertisements
उत्तर
The value of k, corresponding to t1/2 = 10 min = 600 s, is given by
k = `0.693/t_(1//2)`
= `0.693/600`
= 1.155 ×10−3 s−1.
Given that A = 4 × 1013 sec−1 and Ea = 98.6 kJ mol−1.
According to the Arrhenius equation,
k = `e^(-E_a//RT)`
Taking logarithm, we get
loge k = `log_e A - E_a/(RT)`
or, log10 k = `log_10 A - E_a/(2.303 RT)`
Substituting the values, we get
log10 1.155 × 10−3 = `log_10 4 xx 10^13 - 98.6/(2.303 xx 8.314 xx 10^-3 xx 7`
or, −2.9374 = `13.6021 - 5149.6/7`
or, `5149.6/T` = 13.6021 + 2.9374 = 16.5395
or, T = `5149.6/16.5395`
= 311.35 K
APPEARS IN
संबंधित प्रश्न
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)
The activation energy for the reaction \[\ce{2 HI_{(g)} -> H2_{(g)} + I2_{(g)}}\] is 209.5 kJ mol−1 at 581 K. Calculate the fraction of molecules of reactants having energy equal to or greater than activation energy?
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.
Consider a certain reaction \[\ce{A -> Products}\] with k = 2.0 × 10−2 s−1. Calculate the concentration of A remaining after 100 s if the initial concentration of A is 1.0 mol L−1.
The decomposition of hydrocarbon follows the equation k = `(4.5 xx 10^11 s^-1) e^(-28000 K//T)`
Calculate Ea.
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?
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).
What is the effect of adding a catalyst on Activation energy (Ea)
Write a condition under which a bimolecular reaction is kinetically first order. Give an example of such a reaction. (Given : log2 = 0.3010,log 3 = 0.4771, log5 = 0.6990).
The rate of chemical reaction becomes double for every 10° rise in temperature because of ____________.
Activation energy of a chemical reaction can be determined by ______.
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
Thermodynamic feasibility of the reaction alone cannot decide the rate of the reaction. Explain with the help of one example.
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 |
What happens to most probable kinetic energy and the energy of activation with increase in temperature?
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 ______.
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)
A schematic plot of ln Keq versus inverse of temperature for a reaction is shown below

The reaction must be:
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?
Which plot of ln k vs `1/T` is consistent with the Arrhenius equation?
The rate of a reaction quadruples when temperature changes from 27°C to 57°C calculate the energy of activation.
(Given: R = 8. 314 J K−1 mol−1, log 4 = 0.6021)
Assertion (A): A reaction can have zero activation energy.
Reason (R): The minimum extra amount of energy absorbed by reactant molecules so that their energy becomes equal to the threshold value is called activation energy.
In the light of the above statements, choose the correct answer from the options given below:
