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प्रश्न
Thermodynamic feasibility of the reaction alone cannot decide the rate of the reaction. Explain with the help of one example.
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उत्तर
Thermodynamics feasibility of a reaction depends on Gibbs free energy i.e., AG must be negative for spontaneous process. Kinetic feasibility depends on the activation energy of reaction, the lesser is the activation energy, the greater is the feasibility of reaction, i.e.,
i.e., Diamond `->` Graphic ΔG = – ve
This process is thermodynamically feasible but it is very slow due to its high activation energy.
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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 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 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?
Define activation energy.
Explain the following terms :
Half life period of a reaction (t1/2)
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.
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 |
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 ______.
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 activation energy of one of the reactions in a biochemical process is 532611 J mol–1. When the temperature falls from 310 K to 300 K, the change in rate constant observed is k300 = x × 10–3 k310. The value of x is ______.
[Given: ln 10 = 2.3, R = 8.3 J K–1 mol–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.
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]
Which plot of ln k vs `1/T` is consistent with the Arrhenius equation?
Activation energy of any chemical reactions can be calculated if one knows the value of:
