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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

The reaction between HX2(g) and OX2(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.

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प्रश्न

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.

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उत्तर

\[\ce{2H2(g) + O2(g) -> 2H2O(I)}\]

This reaction does not take place at room because the activation energy of the reaction is very high.

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अध्याय 4: Chemical Kinetics - Exercises [पृष्ठ ५६]

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एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
अध्याय 4 Chemical Kinetics
Exercises | Q III. 43. | पृष्ठ ५६

संबंधित प्रश्न

Explain a graphical method to determine activation energy of a reaction.


(b) Rate constant ‘k’ of a reaction varies with temperature ‘T’ according to the equation:

`logk=logA-E_a/2.303R(1/T)`

Where Ea is the activation energy. When a graph is plotted for `logk Vs. 1/T` a straight line with a slope of −4250 K is obtained. Calculate ‘Ea’ for the reaction.(R = 8.314 JK−1 mol−1)


 

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 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.


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). 


 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).


The rate of chemical reaction becomes double for every 10° rise in temperature because of ____________.


Consider figure and mark the correct option.


Oxygen is available in plenty in air yet fuels do not burn by themselves at room temperature. 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

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 ______.


It is generally observed that the rate of a chemical reaction becomes double with every 10°C rise in temperature. If the generalisation holds true for a reaction in the temperature range of 298 K to 308 K, what would be the value of activation energy (Ea) for the reaction?


Which plot of ln k vs `1/T` is consistent with the Arrhenius equation?


The rate of a reaction quadruples when temperature changes from 27°C to 57°C calculate the energy of activation. 

(Given: R = 8. 314 J K−1 mol−1, log 4 = 0.6021)


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