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EnglandChemistrySyllabus dot point

How do we measure and calculate the energy released or absorbed in a chemical reaction?

Enthalpy and standard enthalpy changes, exothermic and endothermic reactions, calorimetry and the q = mcDeltaT equation, average bond enthalpies, and Hess's law including formation and combustion cycles.

An OCR H432 module 3 answer on enthalpy changes: standard enthalpy definitions, calorimetry with q = mcDeltaT, bond enthalpy calculations, and Hess's law cycles for formation and combustion.

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  1. What this topic is asking
  2. Standard enthalpy changes
  3. Calorimetry
  4. Average bond enthalpies
  5. Hess's law
  6. Examples in context
  7. Try this

What this topic is asking

OCR specification point 3.2.1 wants you to define standard enthalpy changes, classify reactions as exothermic or endothermic, measure enthalpy changes by calorimetry using q=mcΔTq = mc\Delta T, calculate enthalpy changes from average bond enthalpies, and apply Hess's law with enthalpy of formation and combustion cycles. This is the start of the physical chemistry that runs through Modules 3 and 5.

Standard enthalpy changes

In an exothermic reaction the products have lower enthalpy than the reactants, so ΔH\Delta H is negative; in an endothermic reaction ΔH\Delta H is positive. Energy is needed to break bonds (endothermic) and released when bonds form (exothermic).

Calorimetry

To get ΔH\Delta H per mole, calculate qq, convert to kJ, divide by the moles reacting, and attach the correct sign (negative for a temperature rise, which signals an exothermic reaction).

Average bond enthalpies

Hess's law

Examples in context

Example 1. Comparing fuels. Calorimetry of different alcohols gives enthalpies of combustion that, per gram, let engineers compare energy density, though heat lost to surroundings always makes the measured value less exothermic than the data-book figure.

Example 2. Why bond-enthalpy answers differ. A value from average bond enthalpies rarely matches the data-book ΔH\Delta H exactly, because real bonds in a specific molecule differ from the averaged values, a point OCR likes you to explain.

Try this

Q1. State what is meant by the standard enthalpy of formation of a compound. [2 marks]

  • Cue. The enthalpy change when one mole of the compound is formed from its constituent elements in their standard states under standard conditions.

Q2. Calculate qq when 200 g200\ \text{g} of water rises by 12.0 C12.0\ ^{\circ}\text{C}. [1 mark]

  • Cue. q=200×4.18×12.0=10,032 J=10.0 kJq = 200 \times 4.18 \times 12.0 = 10{,}032\ \text{J} = 10.0\ \text{kJ}.

Exam-style practice questions

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

OCR 20194 marksA student burned 0.250 g0.250\ \text{g} of ethanol and used the heat to raise the temperature of 150 g150\ \text{g} of water by 18.0 C18.0\ ^{\circ}\text{C}. Calculate the enthalpy of combustion of ethanol in kJ mol1\text{kJ mol}^{-1}. (c=4.18 J g1K1c = 4.18\ \text{J g}^{-1}\text{K}^{-1}, MrM_r ethanol =46.0= 46.0.)
Show worked answer →

Heat absorbed by water q=mcΔT=150×4.18×18.0=11,286 J=11.286 kJq = mc\Delta T = 150 \times 4.18 \times 18.0 = 11{,}286\ \text{J} = 11.286\ \text{kJ} (1).

Moles of ethanol =0.25046.0=5.43×103 mol= \dfrac{0.250}{46.0} = 5.43 \times 10^{-3}\ \text{mol} (1).

ΔcH=11.2865.43×103=2078 kJ mol1\Delta_c H = -\dfrac{11.286}{5.43 \times 10^{-3}} = -2078\ \text{kJ mol}^{-1}, about 2080 kJ mol1-2080\ \text{kJ mol}^{-1} (1). The value is negative because combustion is exothermic (1).

Markers reward q=mcΔTq = mc\Delta T, the moles, the division to get per mole, and the negative sign.

OCR 20213 marksUse the average bond enthalpies H-H=+436\text{H-H} = +436, Cl-Cl=+243\text{Cl-Cl} = +243 and H-Cl=+432 kJ mol1\text{H-Cl} = +432\ \text{kJ mol}^{-1} to calculate the enthalpy change for H2+Cl22HCl\text{H}_2 + \text{Cl}_2 \rightarrow 2\text{HCl}.
Show worked answer →

Bonds broken (reactants): 436+243=+679 kJ mol1436 + 243 = +679\ \text{kJ mol}^{-1} (1).

Bonds made (products): 2×432=864 kJ mol12 \times 432 = 864\ \text{kJ mol}^{-1}, released so 864 kJ mol1-864\ \text{kJ mol}^{-1} (1).

ΔH=(bonds broken)(bonds made)=679864=185 kJ mol1\Delta H = \text{(bonds broken)} - \text{(bonds made)} = 679 - 864 = -185\ \text{kJ mol}^{-1} (1).

Markers reward bonds broken, bonds made, and the subtraction giving an exothermic value.

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