Answer:
Kp = 0.049
Explanation:
The equilibrium in question is;
2 SO₂ (g) + O₂ (g) ⇄ 2 SO₃ (g)
Kp = p SO₃² / ( p SO₂² x p O₂ )
The initial pressures are given, so lets set up the ICE table for the equilibrium:
atm SO₂ O₂ SO₃
I 3.3 0.79 0
C -2x -x 2x
E 3.3 - 2x 0.79 - x 2x
We are told 2x = partial pressure of SO₃ is 0.47 atm at equilibrium, so we can determine the partial pressures of SO₂ and O₂ as follows:
p SO₂ = 3.3 -0.47 atm = 2.83 atm
p O₂ = 0.79 - (0.47/2) atm = .56 atm
Now we can calculate Kp:
Kp = 0.47² /[ ( 2.83 )² x 0.56 ] = 0.049 ( rounded to 2 significant figures )
Note that we have extra data in this problem we did not need since once we setup the ICE table for the equilibrium we realize we have all the information needed to solve the question.
Answer:
4060
Explanation:
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Answer:
2.3 * 10^-5
Explanation:
Recall that the solubility of a solute is the amount of solute that dissolves in 1 dm^3 or 1000cm^3 of solution.
Hence;
Amount of calcium oxalate = 154 * 10^-3/128.097 g/mol = 1.2 * 10^-3 mols
From the question;
1.2 * 10^-3 mols dissolves in 250 mL
x moles dissolves in 1000mL
x = 1.2 * 10^-3 mols * 1000/250
x= 4.8 * 10^-3 moldm^-3
CaC2O4(s) ------->Ca^2+(aq) + C2O4^2-(aq)
Hence Ksp = [Ca^2+] [C2O4^2-]
Where;
[Ca^2+] = [C2O4^2-] = 4.8 * 10^-3 moldm^-3
Ksp = (4.8 * 10^-3)^2
Ksp = 2.3 * 10^-5
Answer:
Use the formula q = m·ΔHv in which q = heat energy, m = mass, and ΔHv = heat of vaporization.
Explanation:
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