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This set of vocabulary flashcards covers concepts related to gaseous equilibria, including partial pressures, mole fractions, the equilibrium constant Kp, and the application of Le Chatelier's principle to industrial processes like the Haber and Contact processes.
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Pascal (Pa)
The SI unit of pressure; 1pascal is a pressure of 1newton per square metre(Nm−2).
Partial pressure (p)
The pressure that an individual gas in a mixture would exert if it occupied the container on its own.
Total pressure
The sum of the partial pressures of all the gases in a mixture.
Mole fraction of a gas A
total number of moles of gas in the mixturenumber of moles of gas A in the mixture
Mathematical expression for partial pressure p of A
partial pressure p of A=mole fraction of A×total pressure
Equilibrium constant Kp
The equilibrium constant for reversible reactions in the gas phase expressed in terms of partial pressures.
Haber process equation
3H2(g)+N2(g)⇌2NH3(g)
Kp unit for the Haber process synthesis
Pa−2
Standard enthalpy change (\Delta H) of the Haber process
−92kJmol−1
Effect of temperature on Kp for exothermic reactions
Increasing the temperature decreases Kp as the equilibrium is forced to the left to absorb heat.
Le Chatelier's principle for pressure in gaseous equilibria
Increasing the pressure forces the equilibrium toward the side with fewer molecules to reduce the total pressure.
Effect of pressure on the equilibrium 2HI(g) ⇌ H2(g) + I2(g)
Pressure has no effect on the equilibrium position because there is no change in the total number of molecules on either side of the reaction.
Effect of increasing pressure on reaction rate
Increases the rate at which equilibrium is reached because there will be more collisions between molecules.
Contact process key stage reaction
2SO2(g)+O2(g)⇌2SO3(g), with ΔH=−197kJmol−1 or −192kJmol−1 as cited in various notes contexts.