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Published on: 13/05/2022
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Questions + Answers key
Take MCQ Chemistry Test1.
Write the differences between rate and rate constant of a reaction.
2.
Calculate the half-life of a first order reaction from their rate constants given below.
(i) 200 S-1
(ii) 2 min-1
(iii) 4 years-1
3.
What is the effect of temperature on the rate constant of a reaction? How can this temperature effect on rate constant be represented quantitatively?
4.
The decomposition of NH3 on platinum surface is zero order reaction what are the rates of production of N2 and H2 if k = 2.5 x10-4 mol + L S-1.
5.
The activation energy of the reaction 2HI(g) ⟶ H2(g) +I2(g) is 209.5 KJ mol-1 at 581 K. Calculate the fraction of molecules of reactants having energy equal to or greater than activation energy.
1.
| S.No | Rate of a reaction | Rate constant of a reaction |
|---|---|---|
| 1. | It represents the speed at which the reactants are converted into products at any instant | It is proportionality constant |
| 2. | It is measured as decrease in the concentration of the reactants or increase in the concentration of products. | It is equal to the rate of reaction when the concentration of each of the reactants in unity. |
| 3. | It depends on the initial concentration of reactants. | It does not depend on the initial concentration of reactants. |
2.
(i) Half life,
= \(\frac { 0.693 }{ 200{ s }^{ -1 } } \)= 3.47s (approximately)
(ii) Half life
= \(\frac { 0.693 }{ 2{ min }^{ -1 } } \) = 0.35 min (approximately)
(iii) Half life,
= \(\frac { 0.693 }{ 2{ 4years }^{ -1 } } \)= 0.173 years (approximately)
3.
(i) The rate constant is nearly doubled with a rise in temperature by 10oC for a chemical reaction.
(ii) The temperature effect on the rate constant can be represented quantitatively by Arrhenius equation.
\(k=A{ e }^{ \frac { -{ E }_{ a } }{ RT } }\)
4.
\(2{ NH }_{ { 3 }_{ (g) } }\overset { pt }{ \longrightarrow } { N }_{ { 2 }_{ (g) } }+3{ H }_{ { 2 }_{ (g) } }\)
Rate = \(-\frac { 1 }{ 2 } \frac { d\left[ { NH }_{ 3 } \right] }{ dt } =\frac { d\left[ { N }_{ 2 } \right] }{ dt } =\frac { 1 }{ 3 } \frac { d\left[ { N }_{ 2 } \right] }{ dt } \)
However, it is given that the reaction is of zero order. Therefore
\(-\frac { 1 }{ 2 } \frac { d\left[ { NH }_{ 3 } \right] }{ dt } =\frac { d\left[ { N }_{ 2 } \right] }{ dt } =\frac { 1 }{ 3 } \frac { d\left[ { N }_{ 2 } \right] }{ dt } k\)
= 2.5 x 10-4 mol L-1 S-1
The rate of production of N2 is
\(\frac { d\left[ { N }_{ 2 } \right] }{ dt } \)= 2.5 x 10-4 mol L-1 S-1
The rate of production of H2 is
\(\frac { d\left[ { N }_{ 2 } \right] }{ dt } \)= 3 x 2.5 x 10-4 mol L-1 s-1
= 7.5 x 10-4 mol L-1 s-1.
5.
In the given case
Ea = 209.5 KJ mol-1 = 209500 J mol-1
T = 581 K
R = 8.314 JK-1 mol-1
Now the fraction of molecules of reactants having energy equal to or greater than activation energy is given as.
x = e-Ea/RT
\(\Rightarrow \log { x } =-\frac { { E }_{ a } }{ RT } \)
\(\Rightarrow \log { x } =-\frac { { E }_{ a } }{ 2.303RT } \)
\(\Rightarrow \log { x } =\frac { 209500J{ mol }^{ -1 } }{ 2.303\times 8.314J{ K }^{ -1 }{ mol }^{ -1 }\times 581 } \)
= 18.8323
x = Antilogs (18.8323)
= Antilogs \(\overset { \_ \_ }{ 19 } .1677\)
= 1.471 x 10-19
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