Advertisements
Advertisements
Questions
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
Solution
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
RELATED QUESTIONS
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 first-order decomposition of H2O2 is given by the following equation:
`logk=14.2-(1.0xx10^4)/TK`
Calculate Ea for this reaction and rate constant k if its half-life period be 200 minutes.
(Given: R = 8.314 JK–1 mol–1)
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 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.
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.
The rate constant of a first order reaction are 0.58 S-1 at 313 K and 0.045 S-1 at 293 K. What is the energy of activation for the reaction?
Define activation energy.
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)
Explain the following terms :
Half life period of a reaction (t1/2)
Activation energy of a chemical reaction can be determined by ______.
Which of the following graphs represents exothermic reaction?
(a)

(b)

(c)

Oxygen is available in plenty in air yet fuels do not burn by themselves at room temperature. Explain.
Why in the redox titration of \[\ce{KMnO4}\] vs oxalic acid, we heat oxalic acid solution before starting the titration?
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 |
The rate constant for a reaction is 1.5 × 10–7 sec–1 at 50°C. What is the value of activation energy?
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 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)
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 ______.
A schematic plot of ln Keq versus inverse of temperature for a reaction is shown below

The reaction must be:
What happens to the rate constant k and activation energy Ea as the temperature of a chemical reaction is increased? Justify.
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:
Given below are two statements:
Statement I: The nutrient deficient water bodies lead to eutrophication.
Statement II: Eutrophication leads to decrease in the level of oxygen in the water bodies.
In the light of the above statements, choose the correct answer from the options given below:
