Sign in to save

Bookmark this page so you can find it later.

Sign in to save

Bookmark this page so you can find it later.

Arrhenius Equation & Activation Energy cheat sheet - grade 11-12

Click image to open full size

Chemistry Grade 11-12

Arrhenius Equation & Activation Energy Cheat Sheet

A printable reference covering the Arrhenius equation, activation energy, rate constants, temperature effects, and Arrhenius plots for grades 11-12.

Download PNG

The Arrhenius equation explains how temperature affects the rate of a chemical reaction. This cheat sheet helps students connect particle collisions, activation energy, and rate constants in one clear reference. It is especially useful for interpreting lab data, comparing reactions, and solving chemistry problems involving temperature changes. Students need it because small temperature changes can cause large changes in reaction rate. The core equation is k=AeEaRTk = Ae^{-\frac{E_a}{RT}}, where kk is the rate constant, AA is the frequency factor, EaE_a is activation energy, RR is the gas constant, and TT is temperature in kelvins. The linear form, lnk=EaR(1T)+lnA\ln k = -\frac{E_a}{R}\left(\frac{1}{T}\right) + \ln A, allows students to find activation energy from a graph. A two-temperature form, ln(k2k1)=EaR(1T21T1)\ln\left(\frac{k_2}{k_1}\right) = -\frac{E_a}{R}\left(\frac{1}{T_2} - \frac{1}{T_1}\right), compares rate constants at two temperatures. Higher activation energy usually means a reaction is more sensitive to temperature changes.

Key Facts

  • The Arrhenius equation is k=AeEaRTk = Ae^{-\frac{E_a}{RT}}, where kk is the rate constant and TT must be measured in kelvins.
  • Activation energy EaE_a is the minimum energy particles must have for a successful reaction to occur.
  • The gas constant is commonly used as R=8.314 J mol1K1R = 8.314\ \text{J mol}^{-1}\text{K}^{-1} when EaE_a is measured in joules per mole.
  • The linear Arrhenius form is lnk=EaR(1T)+lnA\ln k = -\frac{E_a}{R}\left(\frac{1}{T}\right) + \ln A.
  • On a graph of lnk\ln k versus 1T\frac{1}{T}, the slope is m=EaRm = -\frac{E_a}{R}, so Ea=mRE_a = -mR.
  • The two-point Arrhenius equation is ln(k2k1)=EaR(1T21T1)\ln\left(\frac{k_2}{k_1}\right) = -\frac{E_a}{R}\left(\frac{1}{T_2} - \frac{1}{T_1}\right).
  • Temperature must be converted using TK=TC+273.15T_{K} = T_{^{\circ}\text{C}} + 273.15 before using any Arrhenius equation.
  • A catalyst lowers EaE_a, which increases kk at the same temperature without changing the overall reaction energy difference.

Vocabulary

Arrhenius Equation
An equation, k=AeEaRTk = Ae^{-\frac{E_a}{RT}}, that relates a reaction rate constant to temperature and activation energy.
Activation Energy
The minimum energy, EaE_a, that reacting particles must have to form products successfully.
Rate Constant
The value kk that connects reactant concentration to reaction rate for a specific reaction at a specific temperature.
Frequency Factor
The value AA that represents how often particles collide with the proper orientation for reaction.
Arrhenius Plot
A graph of lnk\ln k versus 1T\frac{1}{T} used to determine activation energy from the slope.
Catalyst
A substance that increases reaction rate by providing a lower-energy pathway and reducing EaE_a.

Common Mistakes to Avoid

  • Using Celsius instead of kelvins is wrong because the Arrhenius equation requires absolute temperature, so always convert with TK=TC+273.15T_{K} = T_{^{\circ}\text{C}} + 273.15.
  • Mixing joules and kilojoules is wrong because R=8.314 J mol1K1R = 8.314\ \text{J mol}^{-1}\text{K}^{-1} requires EaE_a in J mol1\text{J mol}^{-1}, not kJ mol1\text{kJ mol}^{-1}.
  • Forgetting the negative slope is wrong because an Arrhenius plot has slope m=EaRm = -\frac{E_a}{R}, so EaE_a must be calculated as Ea=mRE_a = -mR.
  • Using log\log instead of ln\ln without conversion is wrong because the standard Arrhenius forms use natural logarithms, not base-10 logarithms.
  • Assuming a catalyst changes the products is wrong because a catalyst lowers EaE_a and speeds the reaction without changing the balanced equation or overall energy change.

Practice Questions

  1. 1 A reaction has Ea=75.0 kJ mol1E_a = 75.0\ \text{kJ mol}^{-1} and A=2.5×1012 s1A = 2.5 \times 10^{12}\ \text{s}^{-1}. Calculate kk at T=298 KT = 298\ \text{K} using k=AeEaRTk = Ae^{-\frac{E_a}{RT}}.
  2. 2 For an Arrhenius plot of lnk\ln k versus 1T\frac{1}{T}, the slope is 9500 K-9500\ \text{K}. Calculate EaE_a in kJ mol1\text{kJ mol}^{-1} using Ea=mRE_a = -mR.
  3. 3 A reaction has k1=0.015 s1k_1 = 0.015\ \text{s}^{-1} at T1=300 KT_1 = 300\ \text{K} and Ea=48.0 kJ mol1E_a = 48.0\ \text{kJ mol}^{-1}. Use ln(k2k1)=EaR(1T21T1)\ln\left(\frac{k_2}{k_1}\right) = -\frac{E_a}{R}\left(\frac{1}{T_2} - \frac{1}{T_1}\right) to find k2k_2 at T2=330 KT_2 = 330\ \text{K}.
  4. 4 Explain why a reaction with a larger EaE_a usually shows a greater increase in rate when temperature rises.