Advertisements
Advertisements
प्रश्न
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
उत्तर
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))`
or, log 3.333 = 3133.63`(T_2 - 283)/(283 xx T_2)`
or, `0.5228/3133.63 = (T_2 - 283)/(283 xx T_2)`
or, 0.0472T2 = T2 − 283
or, 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.
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 4 × 10−2 to 8 × 10−2 when the temperature changes from 27°C to 37°C. Calculate the energy of activation (Ea). (log 2 = 0.301, log 3 = 0.4771, log 4 = 0.6021)
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 constant for the decomposition of hydrocarbons is 2.418 × 10−5 s−1 at 546 K. If the energy of activation is 179.9 kJ/mol, what will be the value of pre-exponential factor?
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.
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).
A first-order reaction is 50% completed in 40 minutes at 300 K and in 20 minutes at 320 K. Calculate the activation energy of the reaction. (Given : log 2 = 0·3010, log 4 = 0·6021, R = 8·314 JK–1 mol–1)
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).
Consider figure and mark the correct option.
Which of the following graphs represents exothermic reaction?
(a)

(b)

(c)

Thermodynamic feasibility of the reaction alone cannot decide the rate of the reaction. Explain with the help of one example.
Why in the redox titration of \[\ce{KMnO4}\] vs oxalic acid, we heat oxalic acid solution before starting the titration?
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)
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 ______.
A schematic plot of ln Keq versus inverse of temperature for a reaction is shown below

The reaction must be:
