Kp=Kc[RT]
n
Kc=Kp/[RT]
n
n=
moles of gaseous product - moles of gaseous reactant =
3-2=1
625oc=898K
ie: Kc= 0.269/(0.08206 x 898)1
Kc=0.00365
2) For the equilibrium: 2 SO3(g) <=> O2(g) + 2 SO2(g) Kp = 0.269 at 625...
2) For the equilibrium: 2 SO3(g) <=> 02(g) + 2 SO2(g) Kp = 0.269 at 625 °C What is Ke at this temperature? Kp = K[R R = 0.08206 L-atm/mol K (5pts)
For the equilibrium: 2 SO3(g) < = > O2(g) + 2 SO2(g) Kp = 0.269 at 625 oC What is Kc at this temperature? Kp = Kc[RT]Δn R = 0.08206 L-atm/mol K
2) For the equilibrium: 2 SO2(g) + O2(g) < => 2 503(g) Kp = 2.98 at 875oC What is Ke at this temperature? Ko-K[RT]An R = 0.08206 L-atm/mol K (5pts)
5. For the reaction... SO2 + O2 <=> SO3 If the equilibrium position shifts to the right, the concentration of O2 will (2 points) o remain constant increase Decrease
how to solve this?
Sulphur trioxide decomposes at high temperature in a sealed container: 2 SO3(g) <--> 2 SO2(g) + O2(g). Initially, the vessel is charged at 1000 K with SO3(g) at a partial pressure of 0.500 atm. At equilibrium the SO3 partial pressure is 0.200 atm. Calculate the value of Kp at 1000 K to 3 decimal places.
For the reaction 2 SO3 (g) equilibrium reaction arrow 2 SO2 (g) + O2 (g) Kp = 0.335 at 1000 K. Calculate Kc at 1000 K. Please help.
For the equilibrium 2 SO3(g) <----> 2 SO2(g) + O2(g), Kc is 4.08 * 10-3 at 1000 K. Calculate the value for Kp.
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The equilibrium constant in terms of pressures, Kp, for the reaction of SO2 and O2 to form SO3 is 0.365 at 1.15×103 K: SO2(g) + O2(g) = 2SO3(g) A sample of SO3 is introduced into an evacuated container at 298 K and allowed to dissociate until its partial pressure reaches an equilibrium value of 0.867 atm. Calculate the equilibrium partial pressures of SO2 and O2 in the container. PSO2 = PO2 =