Chemistry
Energetics and feasibility
- 1.
Explain the sign of the enthalpy change when a reaction warms its surroundings at constant pressure.
[3 marks] · no calculatorAnswer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- Define the system as the reacting chemicals. A warmer environment has received energy, so the system has lost enthalpy even though the thermometer reading rises.
Marking points
- Heat flows from the reacting system to the surroundings.
- The reaction is exothermic.
- The system's enthalpy change is negative.
Examiner tip: The thermometer's temperature change and reaction enthalpy have opposite signs here.
- 2.
Why does a catalyst not change the enthalpy change of a reaction, even when it makes the reaction faster?
[3 marks] · no calculatorAnswer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- Enthalpy change depends on the difference between final and initial states. Altering the barrier between those states affects rate, not that difference.
Marking points
- It provides an alternative pathway.
- Activation energy is reduced.
- Reactant and product enthalpy levels are unchanged.
Examiner tip: Do not confuse activation energy with reaction enthalpy.
- 3.
A reaction heats 100 g of solution from 20.0 to 26.0 degrees C. Use c = 4.18 J g^-1 K^-1 and 0.0500 mol reacted. Neglect losses and calculate the molar reaction enthalpy.
[3 marks]Answer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- Use q = mc deltaT = 100 x 4.18 x 6. The reaction supplies this heat, so negate it and divide by 0.0500 after converting joules to kilojoules.
Marking points
- Solution heat gain = 2508 J.
- Reaction heat = -2.508 kJ.
- Molar enthalpy = -50.2 kJ mol^-1 to three significant figures.
Examiner tip: Use total solution mass, not the mass of just one reactant.
- 4.
Given deltaHf(CO2) = -394, deltaHf(H2O(l)) = -286 and deltaHf(CH4) = -75 kJ mol^-1, calculate deltaH for CH4 + 2O2 -> CO2 + 2H2O(l).
[3 marks]Answer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- The product total is -394 + 2(-286) = -966. Subtract the reactant total -75: -966 - (-75) = -891 kJ mol^-1.
Marking points
- O2 in its standard state has zero formation enthalpy.
- Use sum(products) minus sum(reactants), including coefficients.
- deltaH = -891 kJ mol^-1.
Examiner tip: The water phase matters; do not substitute a gaseous-water value.
- 5.
For a reaction deltaH = +40.0 kJ mol^-1 and deltaS = +100 J mol^-1 K^-1, assumed constant. Calculate the temperature above which deltaG is negative, and explain why this does not guarantee a fast reaction.
[4 marks]Answer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- At the threshold, set deltaG to zero and solve 40.0/0.100 = 400 K. A positive entropy change favours higher temperature, but feasibility describes the driving force rather than the pathway barrier.
Marking points
- Convert deltaS to 0.100 kJ mol^-1 K^-1.
- Use deltaG = deltaH - T deltaS.
- deltaG < 0 for T > 400 K.
- A large activation barrier may still make the reaction slow.
Examiner tip: Use kelvin, and distinguish zero Gibbs change at the threshold from negative above it.
- 6.
A combustion calorimeter gives a less negative enthalpy than a reliable reference. Explain how incomplete combustion and heat loss each cause this, and propose a distinct improvement for each.
[4 marks] · no calculatorAnswer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- Both errors reduce the magnitude of measured heat, but their causes differ. More oxygen addresses chemical conversion; insulation addresses where released energy goes.
Marking points
- Incomplete combustion releases less energy per mole of fuel than complete combustion.
- Supply sufficient oxygen to improve completeness.
- Heat lost to the room reduces measured temperature rise and calculated heat transfer.
- Use insulation/a shield to reduce environmental heat loss, and a temperature-time cooling correction to account for residual loss.
Examiner tip: Link each improvement to its own error mechanism.
Marking points are indicative, not an official mark scheme. Accept equivalent valid methods and supported interpretations that address the task; award each mark once without requiring the model wording.