Advertisements
Advertisements
प्रश्न
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?
उत्तर
Given: Rate constant k1 = 0.58 s-1
Rate constant k2 = 0.045 s-1
T1 = 313 K
T2 = 293 K
R = 8.314 J K-1mol-1
To find: Activation energy (Ea)
Formula : `log_10 "k"_2/"k"_1 = "E"_"a"/(2.303"R")[("T"_2 - "T"_1)/("T"_1"T"_2")]`
Calculation : From Formula,
`log10((0.045 "s"^-1)/(0.58 "s"^-1)) = "E"_"a"/(2.303 xx 8.314 "JK"^-1 "mol"^-1)[(293"K" - 313 "K")/(293 "K" xx 313 "K")]`
∴ log 0.0776 = `"E"_"a"/(19.147 "J" "mol"^-1)[(-20)/(293 xx 313)]`
∴ `-1.110 = "E"_"a"/19.147[(-20)/(293 xx 313)]`
∴`"E"_"a" = (-1.110 xx 19.147 xx 293 xx 313)/-20`
= 97455.34 J `"mol"^-1`
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 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)
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 rate of the chemical reaction doubles for an increase of 10 K in absolute temperature from 298 K. Calculate Ea.
The activation energy for the reaction \[\ce{2 HI_{(g)} -> H2_{(g)} + I2_{(g)}}\] is 209.5 kJ mol−1 at 581K. Calculate the fraction of molecules of reactants having energy equal to or greater than activation energy?
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 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?
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.
In the Arrhenius equation for a first order reaction, the values of ‘A’ of ‘Ea’ are 4 x 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]
Define activation energy.
The decomposition of a hydrocarbon has value of rate constant as 2.5×104s-1 At 27° what temperature would rate constant be 7.5×104 × 3 s-1if energy of activation is 19.147 × 103 J mol-1 ?
The rate of chemical reaction becomes double for every 10° rise in temperature because of ____________.
Consider figure and mark the correct option.
Which of the following graphs represents exothermic reaction?
(a)
(b)
(c)
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.
Mark the incorrect statements:
(i) Catalyst provides an alternative pathway to reaction mechanism.
(ii) Catalyst raises the activation energy.
(iii) Catalyst lowers the activation energy.
(iv) Catalyst alters enthalpy change of the reaction.
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.
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?
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 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:
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 first-order reaction is 50% complete in 30 minutes at 300 K and in 10 minutes at 320 K. Calculate activation energy (Ea) for the reaction. [R = 8.314 J K−1 mol−1]
[Given: log 2 = 0.3010, log 3 = 0.4771, log 4 = 0.6021]