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A set of vocabulary flashcards based on lecture notes regarding gaseous equilibria, partial pressures, mole fractions, and the factors affecting the equilibrium constant Kp.
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Partial pressure (p)
The pressure that an individual gas in a mixture would exert if it occupied the container on its own; the sum of these pressures equals the total pressure.
Pascal (Pa)
The SI unit of pressure, where 1 pascal is equal to a pressure of 1 newton per square metre (1Nm−2).
Mole fraction of a gas A
The number of moles of gas A in a mixture divided by the total number of moles of gas in the mixture.
Calculation of Partial pressure (p) of A
mole fraction of A×total pressure
Kp
The equilibrium constant for gaseous equilibria, derived from the equilibrium law using partial pressures of reactants and products instead of concentrations.
Equilibrium expression for aA(g)+bB(g)⇌yY(g)+zZ(g)
Kp=paA(g)eqm×pbB(g)eqmpyY(g)eqm×pzZ(g)eqm
Haber process equilibrium
The synthesis of ammonia represented by the equation 3H2(g)+N2(g)⇌2NH3(g), where Kp has units of Pa−2.
Temperature effect on exothermic gaseous equilibrium
For reactions where ΔH is negative (like the Haber process at −92kJmol−1), increasing the temperature decreases the value of Kp and the yield of products.
Pressure effect on gaseous equilibrium
Increasing the total pressure forces the equilibrium toward the side with fewer molecules to reduce the pressure; it only affects the position if there is a change in the total number of molecules.
Rate of gaseous equilibrium
Increasing the pressure or temperature, or using a catalyst, increases the rate at which equilibrium is attained in a gas phase reaction.
Homogeneous systems
Chemical systems, such as gaseous equilibria, where all reactants and products exist in the same phase.