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AP® Chemistry · Unit 6 · Topic 6.2

Energy Diagrams: Study Guide (Chemistry 6.2)

Draw and read energy diagrams that show whether a reaction, phase change or dissolving process is endothermic or exothermic, with a labelled axis, units and a sensible scale.

What an energy diagram shows

In Topic 6.1 you described processes in words: energy moves out of the system (exothermic) or into it (endothermic). An energy diagram shows the same idea as a picture.

  • The vertical axis is the energy of the system, usually in kilojoules per mole, kJ mol⁻¹. “Per mole” means per mole of the process as written in the equation.
  • The horizontal axis shows the progress of the process: start on the left, finish on the right. It has no scale and no unit.
  • A horizontal line (level) marks the energy of each stage: reactants, products, or an intermediate stage.
  • A vertical arrow from the starting level to the final level shows the energy change. In this unit it is written ΔH, the enthalpy change. (Topic 6.6 defines enthalpy properly; for now, read ΔH as the energy change of the system when the process happens at constant pressure.)

The surroundings are not drawn. They are implied: whatever energy the system loses goes to them, and whatever it gains comes from them.

Reading endothermic and exothermic from the levels

Feature Exothermic Endothermic
Products compared with reactants lower higher
Arrow from reactants to products points down points up
Sign of ΔH negative positive
Energy transfer system → surroundings surroundings → system
Effect on the surroundings warm up cool down

ΔH is always found as final level minus starting level:

ΔH = E(products) − E(reactants)

If the products are lower, this difference is negative, which matches energy leaving the system.

Scale and units

An energy diagram is a graph, so it follows graph rules. The vertical axis needs:

  1. A label with a quantity and a unit, such as “Energy (kJ mol⁻¹)”.
  2. Even tick spacing (for example every 50 kJ mol⁻¹), with the numbers written on the ticks.
  3. A range that includes every level you need to draw, with a little space above and below.

Where you put zero is a free choice. Energies of substances are not measured on an absolute scale here; only the differences between levels have meaning. Most students put the reactants at 0, which makes ΔH equal to the products’ level.

Energy diagrams for burning methane and melting ice Two panels, each with a vertical energy axis in kilojoules per mole. Left panel, exothermic, burning methane: the axis runs from minus 1000 to 0 in steps of 200. The level for CH4 gas plus 2 O2 gas is at 0; the level for CO2 gas plus 2 H2O liquid is at about minus 890. A downward arrow between them is labelled delta H about minus 890. Right panel, endothermic, melting ice: the axis runs from 0 to 8 in steps of 2. The level for solid water is at 0 and the level for liquid water is at 6.01. An upward arrow is labelled delta H plus 6.01. Both horizontal axes read before to after. Exothermic: burning methane 0 −200 −400 −600 −800 −1000 Energy (kJ mol⁻¹) ΔH ≈ −890 CH₄(g) + 2O₂(g) CO₂(g) + 2H₂O(l) Endothermic: melting ice 0 2 4 6 8 Energy (kJ mol⁻¹) ΔH = +6.01 H₂O(s) H₂O(l) before → after before → after
Figure 1. Two energy diagrams with very different scales. Left: burning one mole of methane, ΔH about −890 kJ mol⁻¹, so the products lie far below the reactants. Right: melting one mole of ice at 0 °C, ΔH = +6.01 kJ mol⁻¹, so the liquid lies above the solid. Both arrows look a similar length, so you must read the axis numbers, not the arrow length, to compare the two energy changes.

Figure 1 shows why the scale matters. The two arrows are a similar length, but the energy change on the left is about 150 times larger. Each diagram is correct for its own axis. When you compare two processes, draw them on the same axis.

Drawing an energy diagram, step by step

  1. Write the equation with state symbols, and note the value and sign of ΔH.
  2. Draw and label the vertical axis: quantity, unit, even ticks, a range that fits all levels.
  3. Draw the starting level (often at 0) on the left and label it with the reactants.
  4. Draw the final level on the right, at the correct height on your scale, and label it with the products.
  5. Draw the arrow from the starting level to the final level, pointing in the direction of change. Label it with ΔH, including its sign and unit.
  6. Check: products lower and ΔH negative go together; products higher and ΔH positive go together.

Diagrams for physical processes

Energy diagrams are not only for reactions. Any change of a system can be drawn.

Phase changes. For one substance, the gas has the highest energy, then the liquid, then the solid, because attractions between particles lower the energy as the particles come together. So melting and boiling arrows point up (endothermic), and freezing and condensing arrows point down (exothermic). The right panel of Figure 1 is a phase-change diagram.

Dissolving. In Topic 6.1 you split dissolving into three steps. A step diagram shows each step as its own arrow:

  • Step 1, separating solute particles: up.
  • Step 2, separating solvent molecules: up.
  • Step 3, forming solute–solvent attractions: down.

The overall arrow, from the first level to the last, shows whether dissolving is endothermic or exothermic. Worked example 2 draws one.

Diagrams with a hump

In Topic 5.6 you drew energy profiles with a curve that rises to a transition state before falling to the products, and in Topic 5.11 you saw a catalyst lower that hump. A profile is still an energy diagram. The hump shows the activation energy, but the endothermic or exothermic nature depends only on where the curve starts and ends. A catalyst changes the hump, not the two end levels, so it does not change ΔH. If a question asks only “is this exothermic?”, a two-level diagram like Figure 2 is enough.

Worked example 1: drawing a diagram to scale

Question. The fictional reaction J(g) + K₂(g) → JK₂(g) has ΔH = −184 kJ mol⁻¹. (a) Draw an energy diagram to scale. (b) Describe the diagram for the reverse reaction.

  1. Classify. ΔH is negative, so the reaction is exothermic. The product level must be below the reactant level.
  2. Choose the axis. Put the reactants at 0. The product level is −184, so the axis must reach below −184. A range from +50 to −200 kJ mol⁻¹ with ticks every 50 works and leaves space above the reactants for a label.
  3. Place the levels. Reactants on the 0 line. Products at −184, which is about two-thirds of the way from the −150 tick to the −200 tick (34 out of 50).
  4. Draw and label the arrow. Downward, from 0 to −184, labelled “ΔH = −184 kJ mol⁻¹”.
Energy diagram for the fictional reaction J plus K2 forming JK2 Vertical axis: energy in kilojoules per mole, from minus 200 to plus 50 in steps of 50, with dotted grid lines. Horizontal axis: reaction progress, no scale. The reactant level, J gas plus K2 gas, is a line at 0 on the left. The product level, JK2 gas, is a line at minus 184 on the right, a little above the minus 200 tick. A downward arrow from the reactant level to the product level is labelled delta H equals minus 184 kilojoules per mole, energy released to surroundings. 50 0 −50 −100 −150 −200 J(g) + K₂(g) JK₂(g) ΔH = −184 kJ mol⁻¹ (energy released to surroundings) Reaction progress (no scale) Energy (kJ mol⁻¹)
Figure 2. Energy diagram for the fictional reaction J(g) + K₂(g) → JK₂(g), drawn to scale. Energy axis from −200 to +50 kJ mol⁻¹ in steps of 50; dotted lines mark the ticks. The product level sits at −184 kJ mol⁻¹, below the reactants at 0, and the downward arrow shows ΔH.
  1. (b) The reverse reaction, JK₂(g) → J(g) + K₂(g), uses the same two levels. It now starts at the JK₂ level and ends at the J + K₂ level, so the arrow points up and ΔH = +184 kJ mol⁻¹. The reverse reaction is endothermic.

Check. Energy is conserved: the 184 kJ released per mole when JK₂ forms must be supplied to break it apart again.

Worked example 2: a step diagram for dissolving

Question. A fictional salt MQ dissolves in water. Illustrative energy changes for the three steps, per mole of MQ, are: separating the ions, +690 kJ; separating water molecules to make room, +60 kJ; forming ion–water attractions, −770 kJ. (a) Draw a step diagram. (b) Is dissolving MQ endothermic or exothermic? (c) Predict what happens to the temperature of the water.

  1. Start at 0 for solid MQ and water, separately.
  2. Step 1 (up 690): the level for “ions separated” is at +690 kJ mol⁻¹.
  3. Step 2 (up 60): the level for “ions and water molecules separated” is at 690 + 60 = +750 kJ mol⁻¹.
  4. Step 3 (down 770): the final level, MQ(aq), is at 750 − 770 = −20 kJ mol⁻¹.
Step diagram for dissolving the fictional salt MQ Vertical axis: energy in kilojoules per mole, from minus 100 to 900 in steps of 100. The first level, MQ solid plus water, is at 0, and a dashed line extends it across the diagram. Step 1, an upward arrow labelled plus 690, rises to a level labelled ions separated at 690. Step 2, a short upward arrow labelled plus 60, rises to a level labelled ions and water molecules separated at 750. Step 3, a long downward arrow labelled minus 770, falls to the final level, MQ aqueous, at minus 20, just below the dashed starting line. −100 0 100 200 300 400 500 600 700 800 900 Energy (kJ mol⁻¹) MQ(s) + water step 1+690 ions separated ions and water molecules separated step 2: +60 step 3−770 MQ(aq): −20
Figure 3. Step diagram for dissolving the fictional salt MQ, using illustrative values in kJ mol⁻¹. Two upward arrows (steps 1 and 2) take the system from 0 to +750; one long downward arrow (step 3) brings it to −20, just below the dashed line at the starting level.
  1. (b) The final level (−20) is below the starting level (0), so ΔH = −20 kJ mol⁻¹: dissolving MQ is exothermic. The energy released by forming ion–water attractions (770 kJ) is larger than the energy needed for steps 1 and 2 (750 kJ).
  2. (c) Energy moves from the dissolving system into the water, so the temperature of the water rises, though only a little, because the overall change is small.

Point to notice. The overall change is a small difference between two large numbers. If step 3 had been −700 kJ mol⁻¹ instead, the final level would be +50 kJ mol⁻¹ and the same salt would dissolve endothermically. That is why some salts warm water and others cool it.

Worked example 3: a phase-change diagram

Question. A fictional substance K condenses with ΔH = −32 kJ mol⁻¹ and freezes with ΔH = −9 kJ mol⁻¹ (both at the same temperature). Place K(g), K(l) and K(s) on one energy diagram, and find ΔH for K(s) → K(g).

  1. Choose a zero. Put K(g) at 0.
  2. Condensing goes down 32: K(l) is at −32 kJ mol⁻¹.
  3. Freezing goes down a further 9: K(s) is at −32 − 9 = −41 kJ mol⁻¹.
Level Energy with K(g) at 0 (kJ mol⁻¹) Energy with K(s) at 0 (kJ mol⁻¹)
K(g) 0 +41
K(l) −32 +9
K(s) −41 0
  1. Sublimation, K(s) → K(g), starts at the solid level and ends at the gas level: up 41, so ΔH = +41 kJ mol⁻¹ (endothermic).

Check. The second column moves every level up by 41 but keeps every gap the same. Changing the zero never changes an energy change.

Common misconceptions

  • “The arrow goes from the higher level to the lower level.” The arrow always goes from the start of the process to the end. For an endothermic process it points up.
  • “The horizontal axis is time.” It only shows the order of stages. A diagram says nothing about how fast a process is.
  • “A longer arrow always means a bigger energy change.” Only on the same axis. Read the numbers on the scale (Figure 1).
  • “The products must be at a negative number for an exothermic reaction.” Only the products’ position relative to the reactants matters. Reactants at 100 and products at 40 is exothermic.
  • “A catalyst makes a reaction more exothermic.” It lowers the hump, not the end levels, so ΔH is unchanged.
  • “The diagram shows the energy of the surroundings.” It shows the system. The surroundings change by the same amount in the opposite direction.
  • Labelling the vertical axis “Temperature”. The axis is energy, with units of kJ mol⁻¹.

Where this leads

Next, Topic 6.3 explains how energy moves as heat through particle collisions. Energy diagrams return in Topic 6.5 (phase changes), Topic 6.7 (bond enthalpies) and Topic 6.9 (Hess’s law), where step diagrams like Figure 3 help you add energy changes. Try the practice questions now, then use the revision notes and the checklist to consolidate.

Quick questions

Do I have to draw the hump for the activation energy?

Only if the question asks about activation energy or a catalyst. Whether a process is endothermic or exothermic depends only on the start and end levels, so a two-level diagram is enough to show it.

Why is there no unit on the horizontal axis?

The horizontal axis only shows the order of events: before, during and after. It is not time and has no scale, so it has no unit. The vertical axis is the one that needs a label, units and a scale.

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