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3.1Physical Chemistry

Energetics — Edexcel Linear - OL (Chemistry) Revision Notes & Topical Questions

5 min read 14 parts Lesson 4 of 9 Unit quiz

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Curriculum Equation Key قوانين الرقم الهيدروجيني والاتزان الأيوني - pH & Acid-Base Equilibrium FormulasFast Exam Solution
pH = -log[H⁺] | pOH = -log[OH⁻] | pH + pOH = 14 | [H⁺][OH⁻] = 10⁻¹⁴
Word Equation & Conditions: الرقم الهيدروجيني = -لوغاريتم تركيز أيون الهيدروجين | pH + pOH = 14
Location & Specifications: الاتزان الأيوني، كيمياء 3 ثانوي، التحصيلي، و AP Chemistry.
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Lesson summary

Energetics: Exothermic, Endothermic and Energy Profiles — EDEXCEL LINEAR – OL (CHEMISTRY) notes: Describe energy transfers in chemical reactions, draw energy profiles and carry out simple calorimetry practicals.Chemical reactions involve energy changes because bonds break and form.

  • activation energy
  • Worked example 1
  • Worked example 2
  • Worked example 3
  • Worked example 4
  • Calorimeter

Section 1 of 14Energy in chemical reactions

Chemical reactions involve energy changes because bonds break and form. The total energy of a closed system is conserved, so energy lost by the reacting chemicals is gained by the surroundings. Reactions are classified as exothermic (energy to the surroundings, temperature rises) or endothermic (energy from the surroundings, temperature falls).

Exothermic examplesEndothermic examples
Burning fuels, respirationPhotosynthesis (light energy absorbed)
Neutralisation of acid with alkaliThermal decomposition of limestone
Reaction of metals with acidDissolving ammonium nitrate or potassium chloride
Rusting (slow), hand warmersReaction of citric acid with sodium hydrogencarbonate

Section 2 of 14Energy profile diagrams

An energy profile compares the energy of reactants and products.

The vertical axis is energy; the horizontal axis is the course of reaction.
For exothermic reactions products sit below reactants.
For endothermic reactions they sit above.
Activation energy
A hump between represents the activation energy.
A catalyst lowers the hump. ΔH is the vertical difference between reactants and products, negative for exothermic and positive for endothermic.

Section 3 of 14Practical: measuring temperature changes

1
Place 25 cm3 of one reactant (for example 1.0 mol/dm3 hydrochloric acid) in a polystyrene cup inside a beaker.
2
Record the initial temperature of both solutions; they should be equal.
3
Add the other reactant (alkali), put on a lid and stir with the thermometer.
4
Record the highest (or lowest) temperature reached and calculate the temperature change.

Polystyrene is a good insulator and the lid reduces heat loss, giving more accurate results. For a fuel, burn it in a spirit burner under a copper can containing a known mass of water and measure the temperature rise. Results lower than expected arise from heat loss, incomplete combustion and evaporation.

Section 4 of 14Comparing fuels

To compare fuels fairly

  • use the same mass of water and the same distance between the flame and can, burn the same mass of fuel, and calculate energy per gram.
  • Alcohol fuels such as ethanol give less energy per gram than hydrocarbons like octane but are renewable if made from sugar cane;
    • hydrogen releases the most energy per gram and produces only water.

Section 5 of 14Energy changes in everyday life and industry

Energy changes matter in daily life.

1
Self-heating food cans have an exothermic reaction separating the layers of calcium oxide and water.
2
Hand warmers rely on the oxidation of iron powder.
3
Fuel choice depends on the energy released per gram, cost, availability and pollutants: coal and petrol release carbon dioxide and sulfur dioxide,
  • while hydrogen releases only water but is difficult to store.
4
The decomposition of calcium carbonate (CaCO3 → CaO + CO2) needs continuous heat, which is why lime kilns burn large amounts of fuel.

The idea of conservation of energy underlies all of this: energy is not created or destroyed, only transferred from the chemical store of the reactants to thermal energy of the surroundings (exothermic), or from the surroundings to the chemical store of the products (endothermic).

Energy changes in everyday life and industry
When you describe a temperature change in an exam you should say "the energy is released to the surroundings" rather than "the reaction makes heat".
Always link a measured temperature change to the direction of energy transfer and then to the sign of ΔH.

Section 6 of 14Worked examples

  1. Sodium hydroxide solution is added to hydrochloric acid and the temperature rises from 20 °C to 27 °C. Classify the reaction and explain. [2]2 marks

  2. Draw the energy profile for an endothermic reaction. [3]3 marks

  3. A student wants to improve accuracy in the polystyrene cup experiment. Suggest two changes. [2]2 marks

  4. Give one use of an endothermic reaction. [1]1 mark

Section 7 of 14Bond breaking and bond making

Chemical reactions involve rearranging atoms. Energy is needed to break bonds in the reactants (endothermic) and energy is released when new bonds form in the products (exothermic). The overall energy change depends on which is larger:

ConditionOverallΔH
Energy released making bonds > energy needed breaking bondsExothermicNegative
Energy needed breaking bonds > energy released making bondsEndothermicPositive

The bond energy is the energy needed to break one mole of a particular covalent bond in gaseous molecules, in kJ/mol. Stronger bonds have higher bond energies, such as C≡C and N≡N.

Section 8 of 14Step-by-step method

1
Write the balanced equation and draw displayed formulae so that all bonds can be seen.
2
List and total the energy to break all bonds in the reactants.
3
List and total the energy released forming all bonds in the products.
4
ΔH = energy of bonds broken − energy of bonds formed.
5
State whether the reaction is exothermic (negative) or endothermic (positive).

Example

  • N2 + 3H2 → 2NH3 with N≡N 945, H–H 436, N–H 391 kJ/mol.
  • Broken: 945 + 3 × 436 = 2253.
  • Formed: 6 × 391 = 2346.
  • ΔH = 2253 − 2346 = −93 kJ/mol, exothermic.
  • Check: 2 mol of NH3 are formed, so for one mole it is −46.5 kJ/mol.

Section 9 of 14Energy level diagram link and uses

On an energy profile the difference between reactants and products represents ΔH, which can be calculated from bond energies.

Energy level diagram link and uses
The activation energy is not given by this calculation.
Data from bond energies are average values, so the answer may differ from experimental values.
Examples of use: comparing fuels (hydrogen, methane, ethanol), deciding whether a reaction needs heating,
  • and predicting whether a reaction would be hazardous.
    • (such as explosives that release a huge amount of energy as strong bonds in nitrogen gas form)

Section 10 of 14Comparing bond energies and drawing the energy cycle

An alternative layout for the calculation is an energy cycle: reactants to separate atoms (energy in, bonds broken), then separated atoms to products (energy out, bonds formed). ΔH is the sum of the two steps with the correct signs. Many students prefer a table.

BondNumberEnergy each (kJ/mol)Total (kJ/mol)
H–H (broken)34361308
N≡N (broken)1945945
N–H (formed)63912346

Total broken 2253, total formed 2346, ΔH = −93 kJ/mol.

Comparing bond energies and drawing the energy cycle
Tabulating avoids missing bonds.
Notice that the very strong N≡N triple bond makes nitrogen unreactive; breaking it needs 945 kJ/mol,
  • which explains the use of high temperature and a catalyst in the Haber process even though the overall change is exothermic.
Another common trap is the water product: bond energy calculations assume gaseous water; if liquid water is formed, additional energy is released on condensing,
  • so the experimental ΔH is more negative.

Section 11 of 14Worked examples

  1. Calculate ΔH for 2H2 + O2 → 2H2O using H–H 436, O=O 498, O–H 464. [4]4 marks

  2. Explain why the combustion of fuels is exothermic in terms of bonds. [2]2 marks

  3. A reaction breaks bonds requiring 1500 kJ and forms bonds releasing 1200 kJ. Calculate ΔH and classify. [2]2 marks

  4. Why are bond energies only an approximation? [1]1 mark

Section 12 of 14Key terms

TermMeaning
ExothermicReleases energy to the surroundings
EndothermicAbsorbs energy from the surroundings
Activation energyEnergy needed to start the reaction
Energy profileDiagram of energy changes during a reaction
CalorimeterInsulated container for measuring heat changes
SurroundingsEverything outside the reacting chemicals
TermMeaning
Bond energyEnergy to break one mole of a bond
Enthalpy changeΔH, energy change of a reaction
Bonds brokenReactant bonds, energy absorbed
Bonds formedProduct bonds, energy released
Displayed formulaFormula showing all bonds
ExothermicΔH negative

Section 13 of 14Syllabus checklist

CH4 + 2O2 → CO2 + 2H2O.

Extended example: combustion of methane
Bonds broken: 4 C–H (4 × 413 = 1652) and 2 O=O (2 × 498 = 996), total 2648.
  • Bonds formed
    • 2 C=O (2 × 805 = 1610) and 4 O–H (4 × 464 = 1856), total 3466.
    • ΔH = 2648 − 3466 = −818 kJ/mol.
The large negative value explains why methane is a useful fuel.

Section 14 of 14Exam technique

1
Confusing temperature rise with an endothermic reaction.
2
Stating that the energy is destroyed.
3
Drawing the activation energy from products to hump.
4
Not stirring in calorimetry.
1
Subtracting the wrong way round (formed minus broken).
2
Forgetting to count all bonds in a molecule.
3
Saying bond breaking releases energy.
4
Ignoring the stoichiometric coefficients.

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