Chemical Equilibria
Kc Calculations
Expression:
$$K_c = \frac{[PCl_5]}{[PCl_3][Cl_2]}$$
Units:
$$\frac{(mol~dm^{-3})}{(mol~dm^{-3})(mol~dm^{-3})} = \frac{1}{(mol~dm^{-3})} = mol^{-1}dm^{3}$$
First, convert volume to dm3: 200 cm3 = 0.20 dm3.
| Species | PCl3 | Cl2 | PCl5 |
|---|---|---|---|
| Initial Moles | 2.4 | 3.2 | 0.0 |
| Change | -1.1 | -1.1 | +1.1 |
| Eq. Moles | 1.3 | 2.1 | 1.1 |
| Conc (c=n/V) | 6.5 | 10.5 | 5.5 |
$$K_c = \frac{5.5}{(6.5 \times 10.5)} = \frac{5.5}{68.25} = 0.08058…$$
Answer: 0.081 mol-1dm3 (2 s.f.)
The forward reaction is exothermic (negative ΔH). Increasing the temperature favors the endothermic (reverse) reaction to absorb the added heat. This shifts the equilibrium to the left, decreasing the concentration of products and increasing reactants. Therefore, the value of Kc decreases.
Decreasing the volume would increase the pressure, shifting equilibrium to the side with fewer gas moles (the right). However, Kc remains constant because it is temperature-dependent only.
Expression:
$$K_c = \frac{[HBr]^2}{[H_2][Br_2]}$$
Units:
$$\frac{(mol~dm^{-3})^2}{(mol~dm^{-3})(mol~dm^{-3})} = \text{No Units}$$
Since the moles of gas are equal on both sides, volume cancels out. We can calculate using moles directly, but we will use the ICE table method.
| Species | H2 | Br2 | 2HBr |
|---|---|---|---|
| Initial Moles | 12.0 | 12.0 | 0.0 |
| Change | -9.7 | -9.7 | +19.4 |
| Eq. Moles | 2.3 | 2.3 | 19.4 |
$$K_c = \frac{(19.4)^2}{(2.3 \times 2.3)} = \frac{376.36}{5.29} = 71.14…$$
Answer: 71 (2 s.f.)
Increasing pressure has no effect on the position of equilibrium. This is because there are 2 moles of gas on the reactant side and 2 moles of gas on the product side. Pressure only affects equilibrium if there is a difference in gas moles.
Initial Concentrations: [SO2] = 4.00/2.00 = 2.00 M; [O2] = 2.00 M.
| Species (conc) | 2SO2 | O2 | 2SO3 |
|---|---|---|---|
| Initial | 2.00 | 2.00 | 0.00 |
| Change | -1.35 | -0.675 | +1.35 |
| Equilibrium | 0.65 | 1.325 | 1.35 |
$$K_c = \frac{[SO_3]^2}{[SO_2]^2[O_2]} = \frac{(1.35)^2}{(0.65)^2(1.325)} = \frac{1.8225}{0.5598…} = 3.255…$$
Answer: 3.26 mol-1dm3 (3 s.f.)
Rate: The rate at which equilibrium is attained increases because the catalyst provides an alternative pathway with lower activation energy, increasing the frequency of successful collisions.
Position: The position of equilibrium remains unchanged because the catalyst increases the rate of the forward and reverse reactions equally.
Total Volume = 500 cm3 = 0.5 dm3.
Initial Moles: n(FeCl3) = 0.5 × 0.25 = 0.125 mol. n(NH4SCN) = 0.5 × 0.25 = 0.125 mol.
Eq Moles of NH4Cl: n = c × v = 0.12 × 0.5 = 0.06 mol.
| Species | FeCl3 | 3NH4SCN | Fe(SCN)3 | 3NH4Cl |
|---|---|---|---|---|
| Ratio | 1 | 3 | 1 | 3 |
| Initial Mol | 0.125 | 0.125 | 0 | 0 |
| Change | -0.02 | -0.06 | +0.02 | +0.06 |
| Eq. Mol | 0.105 | 0.065 | 0.02 | 0.06 |
| Eq. Conc | 0.21 | 0.13 | 0.04 | 0.12 |
$$K_c = \frac{[Fe(SCN)_3][NH_4Cl]^3}{[FeCl_3][NH_4SCN]^3}$$
$$K_c = \frac{(0.04)(0.12)^3}{(0.21)(0.13)^3} = \frac{0.00006912}{0.000461…} = 0.149…$$
Answer: 0.15 (No Units)
BiCl₃ (aq) + H₂O (l) ⇌ BiOCl (s) + 2HCl (aq)
Important: H2O(l) and BiOCl(s) are not included in the Kc expression.
$$K_c = \frac{[HCl]^2}{[BiCl_3]}$$
Step 1: Initial Moles BiCl3
Mr(BiCl3) = 209 + (3 × 35.5) = 315.5 g/mol.
Moles = 100 / 315.5 = 0.317 mol.
Step 2: ICE Table (Work in Moles)
Eq Moles HCl = 0.20 mol dm-3 × 2.40 dm3 = 0.48 mol.
| Species | BiCl3 | 2HCl |
|---|---|---|
| Initial Mol | 0.317 | 0 |
| Change (1:2) | -0.24 | +0.48 |
| Eq. Mol | 0.077 | 0.48 |
| Conc (n/2.4) | 0.0321 | 0.20 |
$$K_c = \frac{(0.20)^2}{0.0321} = 1.246…$$
Answer: 1.2 mol dm-3
Equilibrium Position: NaOH reacts with HCl (neutralization), lowering the concentration of HCl. The equilibrium shifts to the right to replace the lost product.
Kc: No impact. Kc is constant at a constant temperature.