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प्रश्न
Why does the rate of a reaction increase with rise in temperature?
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उत्तर
At higher temperatures, larger fraction of colliding particles can cross the energy barrier (i.e. the activation energy), which leads to faster rate.
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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 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)
What will be the effect of temperature on rate constant?
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?
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]
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 ?
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.
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.
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 ______.
Explain how and why will the rate of reaction for a given reaction be affected when the temperature at which the reaction was taking place is decreased.
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.
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.
