Chemistry

Temperature Dependence of Rate Constant

Arrhenius Equation

Chemistry
NEET UG
Version 1Updated 22 Mar 2026

The Arrhenius equation is a fundamental formula in chemical kinetics that describes the temperature dependence of reaction rates. Proposed by Svante Arrhenius in 1889, it quantitatively relates the rate constant (kk) of a chemical reaction to the absolute temperature (TT), the activation energy (EaE_a), and a pre-exponential factor (AA). This equation, k=AeEa/RTk = A e^{-E_a/RT}, is pivotal for unders…

Quick Summary

The Arrhenius equation, k=AeEa/RTk = A e^{-E_a/RT}, is a fundamental relationship in chemical kinetics that quantifies how the rate constant (kk) of a reaction changes with absolute temperature (TT). It highlights that reaction rates generally increase exponentially with temperature.

Key components include the pre-exponential factor (AA), representing collision frequency and orientation, and the activation energy (EaE_a), which is the minimum energy barrier reactants must overcome.

The term eEa/RTe^{-E_a/RT} signifies the fraction of molecules possessing sufficient energy to react. A higher EaE_a means a slower reaction, while higher TT leads to a faster reaction. The equation can be linearized as lnk=lnAEaRTln k = ln A - \frac{E_a}{RT}, allowing EaE_a and AA to be determined from an Arrhenius plot of lnkln k versus 1/T1/T.

The slope of this plot is Ea/R-E_a/R. For calculations, temperature must always be in Kelvin, and consistent units for EaE_a and RR are essential. This equation is vital for predicting and controlling reaction rates in various scientific and industrial applications.

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Key Concepts

Activation Energy (EaE_a)

Activation energy is the energy threshold that must be crossed for a chemical reaction to proceed. Imagine a…

Pre-exponential Factor (AA)

The pre-exponential factor, AA, is a composite term that accounts for the frequency of collisions and the…

Arrhenius Plot and its Interpretation

The Arrhenius plot is a powerful tool for experimentally determining EaE_a and AA. By rearranging the…

  • Arrhenius Equation:k=AeEa/RTk = A e^{-E_a/RT}
  • Logarithmic Form:lnk=lnAEaRTln k = ln A - \frac{E_a}{RT}
  • Two-Point Form:ln \frac{k_2}{k_1} = \frac{E_a}{R} left( \frac{1}{T_1} - \frac{1}{T_2} \right)
  • Arrhenius Plot:lnkln k vs 1/T1/T is a straight line.
  • Slope of Arrhenius Plot:EaR-\frac{E_a}{R}
  • Y-intercept of Arrhenius Plot:lnAln A
  • Units:TT in Kelvin (K), EaE_a in extJmol1ext{J mol}^{-1} (if R=8.314,J mol1K1R = 8.314,\text{J mol}^{-1}\text{K}^{-1}).
  • Catalyst Effect:Lowers EaE_a, increases kk.

To remember the Arrhenius equation k=AeEa/RTk = A e^{-E_a/RT}, think: King Arrhenius Explains Energy Required for Transformation.

  • King: kk (rate constant)
  • Arrhenius: AA (pre-exponential factor)
  • Explains: ee (base of natural logarithm)
  • Energy: Ea-E_a (negative activation energy)
  • Required: /R/R (divided by gas constant)
  • Transformation: TT (absolute temperature)
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