Arrhenius equation — calculate activation energy from rate constant data

medium CBSE NEET JEE-MAIN NEET 2023 3 min read

Question

The rate constant of a reaction is 1.5×1031.5 \times 10^{-3} s⁻¹ at 300 K and 4.5×1034.5 \times 10^{-3} s⁻¹ at 320 K. Calculate the activation energy of the reaction. (R=8.314R = 8.314 J mol⁻¹ K⁻¹)

(NEET 2023, similar pattern)


Solution — Step by Step

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

where kk = rate constant, AA = pre-exponential factor, EaE_a = activation energy, RR = gas constant, TT = temperature in Kelvin.

For two temperatures T1T_1 and T2T_2 with rate constants k1k_1 and k2k_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 equivalently using log base 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)

k1=1.5×103k_1 = 1.5 \times 10^{-3} (at T1=300T_1 = 300 K), k2=4.5×103k_2 = 4.5 \times 10^{-3} (at T2=320T_2 = 320 K)

lnk2k1=ln4.5×1031.5×103=ln3=1.0986\ln\frac{k_2}{k_1} = \ln\frac{4.5 \times 10^{-3}}{1.5 \times 10^{-3}} = \ln 3 = 1.0986 1T11T2=13001320=320300300×320=2096000=2.083×104 K1\frac{1}{T_1} - \frac{1}{T_2} = \frac{1}{300} - \frac{1}{320} = \frac{320 - 300}{300 \times 320} = \frac{20}{96000} = 2.083 \times 10^{-4} \text{ K}^{-1}
1.0986=Ea8.314×2.083×1041.0986 = \frac{E_a}{8.314} \times 2.083 \times 10^{-4} Ea=1.0986×8.3142.083×104E_a = \frac{1.0986 \times 8.314}{2.083 \times 10^{-4}} Ea=9.1332.083×104E_a = \frac{9.133}{2.083 \times 10^{-4}} Ea43,850 J/mol43.85 kJ/mol\boxed{E_a \approx 43,850 \text{ J/mol} \approx 43.85 \text{ kJ/mol}}

Why This Works

The Arrhenius equation tells us that only a fraction of molecules have enough energy to cross the activation energy barrier. Higher temperature means more molecules have sufficient energy, so the rate constant increases.

The two-temperature form eliminates the pre-exponential factor AA (which is hard to measure directly). By taking the ratio k2/k1k_2/k_1, the AA cancels out, leaving only EaE_a as the unknown.

A useful check: for most reactions, activation energy falls in the range 40-200 kJ/mol. If your answer is 4 kJ or 4000 kJ, something went wrong with the units.


Alternative Method — Using log₁₀

log4.5×1031.5×103=Ea2.303×8.314×2.083×104\log\frac{4.5 \times 10^{-3}}{1.5 \times 10^{-3}} = \frac{E_a}{2.303 \times 8.314} \times 2.083 \times 10^{-4} log3=0.4771\log 3 = 0.4771 0.4771=Ea19.147×2.083×1040.4771 = \frac{E_a}{19.147} \times 2.083 \times 10^{-4} Ea=0.4771×19.1472.083×104=43,850 J/molE_a = \frac{0.4771 \times 19.147}{2.083 \times 10^{-4}} = 43,850 \text{ J/mol}

For NEET, keep these values ready: ln2=0.693\ln 2 = 0.693, ln3=1.099\ln 3 = 1.099, log2=0.301\log 2 = 0.301, log3=0.477\log 3 = 0.477. Most Arrhenius problems give rate constant ratios of 2 or 3 — knowing these logarithm values saves calculation time.


Common Mistake

Two frequent errors: (1) Getting T1T_1 and T2T_2 mixed up in the formula — always put the lower temperature as T1T_1 and higher as T2T_2. If you swap them, you get a negative EaE_a, which is physically meaningless. (2) Forgetting to convert the final answer from J/mol to kJ/mol when the options are in kJ. Check your answer against the typical range (40-200 kJ/mol) as a sanity check.

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