1) ½ H2 (g) + ½ Cl2 (g) → HCl (g) ΔH° = -92.3 kJ
(2) C (s) + 2 H2 (g) → CH4 (g) ΔH° = -74.8 kJ
(3) C (s) + ½ H2 (g) + 3/2 Cl2 (g) → CHCl3(l) ΔH° = -134.5 kJ
In the formation of methane from chloroform, we need to reverse equation (3) since it has chloroform as a product, and we want it as a reactant. When you reverse this reaction, the sign of ΔH° will change from - to +.
(3) CHCl3 (l) → C (s) + ½ H2 (g) + 3/2 Cl2 (g) ΔH° = +134.5 kJ
Equation (2) will remain as is since methane is on the product side.
Reverse equation (1) since HCl has to be on the reactant side.
(1) HCl (g) → ½ H2 (g) + ½ Cl2 (g) ΔH° = +92.3 kJ
Multiply equation (1) by a factor of 3 since we need 3 moles of HCl in the formation of methane.
(1) [ HCl (g) → ½ H2 (g) + ½ Cl2 (g) ΔH° = +92.3 kJ ] x 3
So it becomes,
(1) 3 HCl (g) → 3/2 H2 (g) + 3/2 Cl2 (g) ΔH° = +276.9 kJ
We use all 3 equations, are
(1) 3 HCl (g) → 3/2 H2 (g) + 3/2 Cl2 (g) ΔH° = +276.9 kJ
(2) C (s) + 2 H2 (g) → CH4 (g) ΔH° = -74.8 kJ
(3) CHCl3 (l) → C (s) + ½ H2 (g) + 3/2 Cl2 (g) ΔH° = +134.5 kJ
3 HCl (g) + C (s) + 2 H2 (g) + CHCl3 (l) → 3/2 H2 (g) + 3/2 Cl2 (g) + CH4 (g) + C (s) + ½ H2 (g) + 3/2 Cl2 (g)
The net reaction after canceling and adding the coefficients of the common reactants / products will give:
CHCl3 (l) + 3 HCl (g) → CH4 (g) + 3 Cl2 (g)
ΔH° = +276.9 kJ - 74.8 kJ + 134.5 kJ
∆H° = +336.6 kJ
the change in the enthalpy of the formation of methane, CH4, using chloroform, CHC13, ∆H° = +336.6 kJ.
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