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Chemical Kinetics and Nuclear Chemistry question

2009 · Shift 2 · Q1
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Chemical Kinetics and Nuclear Chemistry question

2009 · Shift 2 · Q1

JEE AdvancedChemistryChemical Kinetics and Nuclear ChemistryMCQ+3 / −1
For a first-order reaction A →\to→ P, the temperature (T) dependent rate constant (k) was found to follow the equation log⁡k=−(2000)1T+6.0\log k = - (2000){1 \over T} + 6.0logk=−(2000)T1​+6.0. The pre-exponential factor A and activation energy EaE_aEa​, respectively, are
  1. A
    1.0×106 s−11.0\times10^6~\mathrm{s^{-1}}1.0×106 s−1 and 9.2 kJ mol −1{}^{-1}−1
  2. B
    6.0 s−16.0~\mathrm{s^{-1}}6.0 s−1 and 16.6 kJ mol −1{}^{-1}−1
  3. C
    1.0×106 s−11.0\times10^6~\mathrm{s^{-1}}1.0×106 s−1 and 16.6 kJ mol −1{}^{-1}−1
  4. D
    1.0×106 s−11.0\times10^6~\mathrm{s^{-1}}1.0×106 s−1 and 38.3 kJ mol −1{}^{-1}−1
View written solutionFree

Correct answer: D

  1. Use the Arrhenius equation in logarithmic form

For a reaction,

k=Ae−Ea/(RT)k = A e^{-E_a/(RT)}k=Ae−Ea​/(RT)

Taking common logarithm,

log⁡k=log⁡A−Ea2.303RT\log k = \log A - \frac{E_a}{2.303RT}logk=logA−2.303RTEa​​
  1. Compare with the given equation

Given:

log⁡k=−2000T+6.0\log k = -\frac{2000}{T} + 6.0logk=−T2000​+6.0

Comparing with

log⁡k=log⁡A−Ea2.303RT\log k = \log A - \frac{E_a}{2.303RT}logk=logA−2.303RTEa​​

we get:

  • Intercept: log⁡A=6.0\log A = 6.0logA=6.0
  • Slope term: Ea2.303R=2000\frac{E_a}{2.303R} = 20002.303REa​​=2000
  1. Calculate the pre-exponential factor AAA

Since

log⁡A=6.0\log A = 6.0logA=6.0

therefore,

A=106 s−1A = 10^6~\mathrm{s^{-1}}A=106 s−1
  1. Calculate the activation energy EaE_aEa​
Ea=2000×2.303×RE_a = 2000 \times 2.303 \times REa​=2000×2.303×R

Using R=8.314 J mol−1 K−1R = 8.314~\mathrm{J~mol^{-1}~K^{-1}}R=8.314 J mol−1 K−1,

Ea=2000×2.303×8.314E_a = 2000 \times 2.303 \times 8.314Ea​=2000×2.303×8.314 Ea≈38288 J mol−1E_a \approx 38288~\mathrm{J~mol^{-1}}Ea​≈38288 J mol−1 Ea≈38.3 kJ mol−1E_a \approx 38.3~\mathrm{kJ~mol^{-1}}Ea​≈38.3 kJ mol−1
  1. Match with the options

Thus,

A=1.0×106 s−1,Ea=38.3 kJ mol−1A = 1.0\times10^6~\mathrm{s^{-1}}, \qquad E_a = 38.3~\mathrm{kJ~mol^{-1}}A=1.0×106 s−1,Ea​=38.3 kJ mol−1

This corresponds to Option D.

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