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Slav-nsk [51]
2 years ago
7

Using table 9.4, calculate an approximate enthalpy (in kj) for the reaction of 1.02 g gaseous methanol (ch3oh) in excess molecul

ar oxygen to form gaseous carbon dioxide and gaseous water. (hint, remember to first write the balanced equation.)
Chemistry
1 answer:
Tanya [424]2 years ago
6 0

<u>Given:</u>

Mass of methanol = 1.02 g

<u>To determine:</u>

Enthalpy for the reaction of 1.02 g of methanol with excess O2

<u>Explanation:</u>

Balanced equation-

2CH3OH(g) + 3O2(g) → 2CO2(g) + 4H2O(g)

The reaction enthalpy is given as:

ΔHrxn = ∑nH°f(products) - ∑nH°f(reactants)

where n = number of moles

H°f = standard enthalpy of formation.

ΔHrxn = [2H°f(CO2(g)) + 4H°f(H2O(g))] - [2H°f(CH3OH(g)) + 3H°f(O2(g))]

           = [2(-393.5) + 4(-241.8)]-[2(-201.5) + 3(0)] = -1351.2 kJ

Now, 1 mole of CH3OH = 32 g

The calculated ΔHrxn corresponds to 2 moles of CH3OH. i.e.

The enthalpy change for 64 g of Ch3OH = -1351.2 kJ

Therefore, for 1.02g gaseous methanol we have:

ΔH = 1.02 * -1351.2/64 = -21.5 kJ

Ans: The enthalpy for the given reaction is -21.5 kJ



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C. ΔG° = -58.59 kJ

Explanation:

Let's consider the following reaction.

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We can calculate the standard Gibbs free energy of the reaction (ΔG°) using the following expression.

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<h3>A. 285 K</h3>

ΔG° = ΔH° - T.ΔS°

ΔG° = 178.3 kJ - 285K × 0.1606 kJ/K = 132.5 kJ

<h3>B. 1025 K</h3>

ΔG° = ΔH° - T.ΔS°

ΔG° = 178.3 kJ - 1025K × 0.1606 kJ/K = 13.69 kJ

<h3>C. 1475 K</h3>

ΔG° = ΔH° - T.ΔS°

ΔG° = 178.3 kJ - 1475K × 0.1606 kJ/K = -58.59 kJ

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