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What does a reaction energy profile show about activation energy, the transition state and the enthalpy of reaction?

Topic 5.6 Reaction Energy Profile: interpret a potential-energy diagram to identify the activation energy of the forward and reverse reactions, the transition state and the enthalpy of reaction.

A focused answer to AP Chemistry Topic 5.6, covering the potential-energy diagram, the transition state, the activation energy of the forward and reverse reactions, the relationship to enthalpy of reaction, and the effect of a catalyst, with full worked examples.

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  1. What this topic is asking
  2. Reading the diagram
  3. Activation energies, forward and reverse
  4. Enthalpy of reaction
  5. The effect of a catalyst
  6. Try this

What this topic is asking

The College Board (Topic 5.6) wants you to read a potential-energy diagram (reaction energy profile) and identify the activation energy of the forward and reverse reactions, the transition state, and the enthalpy of reaction. These diagrams unify kinetics (the barrier height, which controls rate) and thermodynamics (the energy difference between reactants and products) on one picture.

Reading the diagram

The transition state is the highest-energy point on the path, an unstable arrangement in which old bonds are partly broken and new bonds partly formed. It is not an isolable species and not the same as an intermediate, which sits in a valley between two peaks (Topic 5.10).

Activation energies, forward and reverse

Because both reactions go over the same barrier, the peak is shared. For an exothermic reaction the products are lower than the reactants, so the reverse barrier is taller than the forward one; for an endothermic reaction the forward barrier is taller. Reading off both activation energies from a labelled diagram is a routine FRQ skill.

Enthalpy of reaction

The enthalpy of reaction is the vertical difference between products and reactants:

ΔH=EproductsEreactants\Delta H = E_{\text{products}} - E_{\text{reactants}}

If the products lie below the reactants the reaction is exothermic (ΔH<0\Delta H < 0); if above, endothermic (ΔH>0\Delta H > 0). This connects to Unit 6: the height of the barrier (kinetics) is independent of the sign of ΔH\Delta H (thermodynamics), so a strongly exothermic reaction can still be slow if its activation energy is high.

The effect of a catalyst

A catalyst provides an alternative pathway with a lower transition-state energy, so it lowers both the forward and reverse activation energies by the same amount and speeds both directions. Crucially it leaves the reactant and product energies untouched, so the enthalpy of reaction and the position of equilibrium are unchanged. The catalyst is drawn as a lower (or split) peak on the same diagram.

Try this

Q1. A reaction has forward Ea=90. kJ mol1E_a = 90.\ \text{kJ mol}^{-1} and ΔH=30. kJ mol1\Delta H = -30.\ \text{kJ mol}^{-1}. Calculate the reverse activation energy. [2 points]

  • Cue. Ea,reverse=Ea,forwardΔH=90.(30.)=120. kJ mol1E_{a,\text{reverse}} = E_{a,\text{forward}} - \Delta H = 90. - (-30.) = 120.\ \text{kJ mol}^{-1}.

Q2. Explain why a catalyst changes the activation energy but not the enthalpy of reaction. [2 points]

  • Cue. It lowers the transition-state energy (a new pathway), but the reactant and product energies are fixed, so ΔH=EproductsEreactants\Delta H = E_\text{products} - E_\text{reactants} is unchanged.

Exam-style practice questions

Practice questions written in the style of College Board exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.

AP 2022 (style)4 marksSection II (long FRQ, part). For a single-step reaction, the reactants lie at 80. kJ mol180.\ \text{kJ mol}^{-1}, the peak at 200. kJ mol1200.\ \text{kJ mol}^{-1}, and the products at 120. kJ mol1120.\ \text{kJ mol}^{-1} on a potential-energy diagram. (a) Calculate the activation energy of the forward reaction. (b) Calculate the activation energy of the reverse reaction. (c) Calculate the enthalpy change of the forward reaction and state whether it is endothermic or exothermic. (d) Justify how adding a catalyst would change parts (a) and (c).
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A 4-point quantitative FRQ on an energy profile.

(a) Forward EaE_a (1 point): peak minus reactants =200.80.=120. kJ mol1= 200. - 80. = 120.\ \text{kJ mol}^{-1}.
(b) Reverse EaE_a (1 point): peak minus products =200.120.=80. kJ mol1= 200. - 120. = 80.\ \text{kJ mol}^{-1}.
(c) Enthalpy (1 point): products minus reactants =120.80.=+40. kJ mol1= 120. - 80. = +40.\ \text{kJ mol}^{-1}; positive, so endothermic.
(d) Catalyst (1 point): a catalyst lowers both forward and reverse activation energies by providing a lower-energy pathway, so part (a) would decrease; it does not change the reactant or product energies, so ΔH\Delta H in part (c) is unchanged.

Markers reward both activation energies, the enthalpy with its sign and label, and the reasoning that a catalyst lowers EaE_a but leaves ΔH\Delta H unchanged.

AP 2021 (style)1 marksSection I (multiple choice). On a potential-energy diagram, the transition state is located at (A) the energy of the reactants (B) the energy of the products (C) the highest point of the curve (D) the lowest point of the curve. Justify your choice.
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A 1-point conceptual MCQ. The answer is (C).

The transition state is the highest-energy arrangement along the reaction path, the unstable configuration of partially broken and formed bonds at the top of the energy barrier. The trap is confusing it with a reaction intermediate, which sits in a valley, not at the peak.

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