Relationship between ln k and 1/t using different formula

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SUMMARY

The discussion centers on the relationship between ln k and 1/t in the context of the Arrhenius equation and its implications for chemical kinetics and equilibrium. The confusion arises from the distinction between the rate constant (k) and the equilibrium constant (K), where k pertains to reaction kinetics and K pertains to thermodynamic equilibrium. The slopes derived from these equations yield different interpretations, specifically -Ea/R for activation energy and -H/R for enthalpy change, leading to the conclusion that they represent different constants. Understanding this distinction is crucial for accurately interpreting experimental data in chemistry.

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  • Understanding of the Arrhenius equation
  • Familiarity with concepts of activation energy and enthalpy
  • Basic knowledge of chemical kinetics and thermodynamics
  • Ability to perform linear regression analysis
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  • Study the Arrhenius equation in detail, focusing on its application in chemical kinetics
  • Explore the differences between rate constants (k) and equilibrium constants (K)
  • Learn about linear regression techniques in the context of chemical data analysis
  • Investigate the implications of activation energy and enthalpy in exothermic reactions
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Chemistry students, educators, and researchers interested in the nuances of chemical kinetics and thermodynamics, particularly those studying reaction mechanisms and equilibrium analysis.

Ethan Cheng
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Hi, I'm currently taking Chemistry 101 and came across this equation that seems to contradict what I've learned before. I don't know the name of it, but here is the equation and its implication.
Chem 1.PNG
Chem 2.PNG

Now another equation we have learned is the Arrhenius equation, which is as follows:
arrhenius%20plot1.jpg


If I understood the equations correctly, they are referring to the same k (equilibrium constant) and the same t (temperature), which gave rise to something that seems to be wrong.

Take the example of combustion, where the activation energy is above 0 and is an exothermic reaction. The graph produced by the first equation will be one with a positive slope, but the one produced by the second equation is one with a negative slope, even though they have the same axis. To illustrate this further, if we somehow experimentally determined the ln k and 1/t (appears very often in our homework), we usually start by graphing them. The linear regression is seen (using Arrhenius equation) as -Ea/R, and we can, therefore, use it to find activation energy. But this same slope should also be -H / R, and therefore will lead to Ea = H, which is also obviously wrong.

What am I missing here? Are the K referring to different values?
 

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The equation in your first figures refers to the equilibrium constant and the heat of reaction. The equation in your 2nd figure refers to the reaction rate constant and the activation energy for the reaction.
 
Ethan Cheng said:
Are the K referring to different values?

Yes. One is often written as k (for kinetics), the other as K (for equilibrium).
 

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