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Flashcards · 9620 · A Level Topic 12
Equilibrium constant Kp for homogeneous systems (A Level) flashcards
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3.1.12.1 Equilibrium constant Kp for homogeneous systems
- Mole fraction and partial pressure
- Mole fraction of A = n(A) ÷ total moles of gas (no units). Partial pressure of A = mole fraction of A × total pressure.
- Kp expression for 2NO₂(g) ⇌ 2NO(g) + O₂(g)
- Kp = p(NO)² × p(O₂) ÷ p(NO₂)². With pressures in kPa, units are kPa (Δn = +1).
- How do you work out the units of Kp?
- (pressure unit)^Δn, where Δn = moles of gaseous products − moles of gaseous reactants. No units if Δn = 0.
- Effect of raising total pressure on Kp and on the equilibrium position
- Kp is unchanged. The position shifts towards the side with fewer moles of gas.
- Kp increases when the temperature rises. Is the forward reaction exothermic or endothermic?
- Endothermic: the rise in temperature moved the equilibrium right, in the endothermic direction.
- A gas mixture has 0.270 mol of one gas in 0.900 mol total at 250 kPa. Partial pressure of that gas?
- Mole fraction = 0.270 ÷ 0.900 = 0.300; partial pressure = 0.300 × 250 = 75.0 kPa.
Revise Equilibrium constant Kp for homogeneous systems further
- Study guideOxfordAQA A-Level Chemistry: Equilibrium constant Kp for homogeneous systems (9620)
- Revision notesOxfordAQA A-Level Chemistry: Equilibrium constant Kp for homogeneous systems (9620) – Revision Notes
- Practice questionsOxfordAQA A-Level Chemistry: Equilibrium constant Kp for homogeneous systems (9620) – Practice Questions