Chemistry · 9. Chemical energetics
Exothermic and endothermic reactions and enthalpy
Track energy transfer and use simple calorimetry and Hess’s law to calculate enthalpy changes.
Driving question
How can a measured temperature change reveal the energy change of a reaction?
Curriculum coverage
Vietnam Chemistry 10; Cambridge IGCSE 0620 and AS & A Level 9701: energetics, calorimetry and Hess cycles.
Model scope and limitations
Simple cup calorimetry often assumes solution density 1.00 g/cm³ and specific heat capacity 4.18 J g⁻¹ K⁻¹; heat loss and apparatus heat capacity shift results from standard values. The simulation illustrates direction of change and does not replace calibrated calorimetry data.
Learning objectives
- Distinguish system from surroundings and determine the sign of ΔH.
- Use q = mcΔT and ΔH = −q/n with consistent units.
- Apply Hess’s law and bond energies with the correct break–make convention.
Prerequisite knowledge
- Moles, balanced equations and J–kJ conversion.
- Temperature, mass and specific heat capacity.
Core knowledge
Sign of ΔH
An exothermic reaction transfers energy from system to surroundings, so ΔHsystem < 0; an endothermic reaction absorbs energy, so ΔHsystem > 0.
Calorimetry
The solution gains qsolution = mcΔT. Neglecting losses, qreaction = −qsolution and ΔH = qreaction/n for the defined amount of reaction.
Hess’s law
Enthalpy is a state function, so overall ΔH is the algebraic sum of steps; reversing an equation changes the sign and scaling it scales ΔH.
Worked example
Mixing 50.0 cm³ of 1.00 mol/dm³ HCl and 50.0 cm³ of 1.00 mol/dm³ NaOH raises temperature by 6.80 K. With m = 100 g and c = 4.18 J g⁻¹ K⁻¹, qsolution = 2842 J. As 0.0500 mol H₂O forms, ΔH = −2.842/0.0500 = −56.8 kJ mol⁻¹.
Misconceptions to avoid
- A temperature rise does not mean positive system ΔH; the surroundings warm because the reacting system loses energy.
- Bond formation releases energy whereas bond breaking requires it; using mean bond enthalpies, ΔH ≈ energy to break − energy released on forming.
- A temperature interval has the same numerical size in kelvin and Celsius, but absolute temperatures are not interchangeable without conversion.
Virtual experiment procedure: Zinc–acid reaction and thermal change
- In the Zn–HCl simulation, identify system and surroundings and predict the sign of ΔH before mixing.
- Record observations and the direction of temperature change; do not invent measurements if the simulation has no quantitative sensor.
- Use the lesson calorimetry data to calculate q, limiting moles and ΔH, then state a directional source of error.
Safety and cautions
- Metal–acid reactions produce flammable H₂ and may splash acid; real work requires eye protection, ventilation and no ignition source near the reaction vessel.
Evidence to collect
- An energy-transfer diagram showing system, surroundings and the sign of ΔH.
- A unit-labelled q and ΔH calculation with reacting moles and at least one assumption or heat-loss source.
Diagnostic check
1. A reaction that warms the surroundings normally has what system ΔH?
Show answer and explanation
Correct answer: Negative
Energy leaves the system, so system enthalpy decreases.
2. In q = mcΔT, what is a suitable unit for c?
Show answer and explanation
Correct answer: J g⁻¹ K⁻¹
Specific heat capacity is energy per mass per temperature interval.
3. When a Hess equation is reversed, what happens to ΔH?
Show answer and explanation
Correct answer: Change its sign
The reverse path transfers the same energy in the opposite direction.
Application practice
1. A 100 g solution warms by 5.0 K with c = 4.18 J g⁻¹ K⁻¹. How much heat does it gain?
Show answer and explanation
Correct answer: 2.09 kJ
q = 100×4.18×5.0 = 2090 J = 2.09 kJ.
2. If 0.050 mol of reaction releases 2.85 kJ, what is the molar ΔH?
Show answer and explanation
Correct answer: −57 kJ mol⁻¹
ΔH = −2.85/0.050 = −57 kJ mol⁻¹; negative because the reaction releases heat.
3. For an exothermic calorimetry experiment, heat loss to the room usually makes measured |ΔH| do what?
Show answer and explanation
Correct answer: Smaller than the true value
The observed ΔT is too small, so q and the magnitude of ΔH are underestimated.
Academic references
- Cambridge IGCSE Chemistry 0620 — official syllabus and resources
- Cambridge AS & A Level Chemistry 9701 — official syllabus
- OpenStax Chemistry 2e — peer-reviewed general chemistry
- IUPAC Color Books — authoritative chemical terminology and nomenclature
- BIPM — SI Brochure, 9th edition
This lesson is maintained against the cited sources below. Simulations are learning models and do not replace supervised physical-laboratory safety procedures.
- Content publisher
- WebLab STEM
- Technical maintainer
- Đức Tiến — Control & Automation Engineer