Effect of temperature on reaction rate — Arrhenius equation graphically explained

medium CBSE JEE-MAIN NEET 3 min read

Question

How does temperature affect reaction rate? What is the Arrhenius equation, and how do we use it to calculate activation energy from experimental data?

(JEE Main, NEET, CBSE 12 — Arrhenius equation numericals are high-frequency questions in both JEE and NEET)


Solution — Step by Step

A common rule of thumb: for every 10 degC rise in temperature, the reaction rate roughly doubles. This is called the temperature coefficient.

But why? At higher temperature, molecules move faster, collide more frequently, and — more importantly — a larger fraction of molecules have energy exceeding the activation energy (EaE_a). This second factor is the dominant one.

k=AeEa/RTk = A \cdot e^{-E_a/RT}

where:

  • kk = rate constant
  • AA = pre-exponential factor (frequency factor, related to collision frequency and orientation)
  • EaE_a = activation energy (J/mol)
  • RR = gas constant (8.314 J/mol/K)
  • TT = temperature in Kelvin

Taking natural log of both sides:

lnk=lnAEaRT\ln k = \ln A - \frac{E_a}{RT}

This is the equation of a straight line: plot lnk\ln k vs 1/T1/T, and you get:

  • Slope = Ea/R-E_a/R (from which we calculate EaE_a)
  • y-intercept = lnA\ln A

If we know kk at two temperatures T1T_1 and T2T_2:

lnk2k1=EaR(1T11T2)\ln\frac{k_2}{k_1} = \frac{E_a}{R}\left(\frac{1}{T_1} - \frac{1}{T_2}\right)

Or using log10\log_{10}:

logk2k1=Ea2.303R(1T11T2)\log\frac{k_2}{k_1} = \frac{E_a}{2.303R}\left(\frac{1}{T_1} - \frac{1}{T_2}\right)

Worked example: A reaction has k1=2×103k_1 = 2 \times 10^{-3} s1^{-1} at 300 K and k2=8×103k_2 = 8 \times 10^{-3} s1^{-1} at 320 K. Find EaE_a.

log8×1032×103=Ea2.303×8.314(13001320)\log\frac{8 \times 10^{-3}}{2 \times 10^{-3}} = \frac{E_a}{2.303 \times 8.314}\left(\frac{1}{300} - \frac{1}{320}\right) log4=Ea19.15(320300300×320)\log 4 = \frac{E_a}{19.15}\left(\frac{320-300}{300 \times 320}\right) 0.602=Ea19.15×20960000.602 = \frac{E_a}{19.15} \times \frac{20}{96000} 0.602=Ea19.15×2.083×1040.602 = \frac{E_a}{19.15} \times 2.083 \times 10^{-4} Ea=0.602×19.152.083×104=55,340 J/mol55.3 kJ/molE_a = \frac{0.602 \times 19.15}{2.083 \times 10^{-4}} = 55,340 \text{ J/mol} \approx \mathbf{55.3 \text{ kJ/mol}}
flowchart TD
    A["Temperature increases"] --> B["More molecules exceed Ea"]
    B --> C["Rate constant k increases exponentially"]
    C --> D["Reaction rate increases"]
    E["Arrhenius Plot"] --> F["Plot ln k vs 1/T"]
    F --> G["Straight line with negative slope"]
    G --> H["Slope = -Ea/R"]
    H --> I["Calculate Ea = -slope × R"]

Why This Works

The exponential factor eEa/RTe^{-E_a/RT} represents the fraction of molecules with kinetic energy greater than EaE_a (from the Maxwell-Boltzmann distribution). At low temperatures, this fraction is tiny. A small increase in TT dramatically increases this fraction because it appears in the exponent. This is why temperature has such a powerful effect on reaction rates — it is not linear but exponential.

The Arrhenius equation unifies two observations: reactions with high EaE_a are slow (large exponent), and raising temperature speeds them up (smaller effective exponent).


Common Mistake

The unit trap: EaE_a must be in J/mol (not kJ/mol) when using R=8.314R = 8.314 J/mol/K in the Arrhenius equation. If the question gives EaE_a in kJ/mol, multiply by 1000 before substituting. Alternatively, use R=8.314×103R = 8.314 \times 10^{-3} kJ/mol/K. Mixing units is the number one source of wrong answers in Arrhenius numericals.

For quick estimation: if the rate doubles for a 10 degC rise (temperature coefficient = 2), the activation energy is approximately 53 kJ/mol at room temperature. Most reactions tested in exams have EaE_a between 40-100 kJ/mol. If your calculated answer falls outside this range, double-check your units.

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