Chapter 5: Problem 51
From the following heats of combustion, \(\begin{aligned} \mathrm{CH}_{3} \mathrm{OH}(l)+\frac{3}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(l) & \Delta H_{\mathrm{rxn}}^{\circ}=-726.4 \mathrm{~kJ} / \mathrm{mol} \\\ \mathrm{C}(\text { graphite })+\mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g) & \\ \Delta H_{\mathrm{rxn}}^{\circ}=-393.5 \mathrm{~kJ} / \mathrm{mol} \\ \mathrm{H}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l) & \\ \Delta H_{\mathrm{rxn}}^{\circ}=-285.8 \mathrm{~kJ} / \mathrm{mol} \end{aligned}\) calculate the enthalpy of formation of methanol \(\left(\mathrm{CH}_{3} \mathrm{OH}\right)\) from its elements: $$ \mathrm{C}(\text { graphite })+2 \mathrm{H}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{CH}_{3} \mathrm{OH}(l) $$
Short Answer
Step by step solution
Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Heats of Combustion
In this context, every chemical equation provided has an associated enthalpy change, labeled as \( \Delta H_{\text{rxn}}^{\circ}\). This symbol represents the standard enthalpy change of the combustion reaction in kilojoules per mole. For example, the combustion of methanol is associated with a heat release of \( -726.4 \, \mathrm{kJ} / \mathrm{mol}\). Heats of combustion are measured in controlled environments to ensure that the pressure and temperature remain constant, typically at standard conditions (298 K and 1 atm).
Understanding the heat of combustion allows us to calculate other related thermodynamic quantities, such as the enthalpy of formation. By applying conservation of energy principles and Hess's Law, we can deduce the desired enthalpy values from known heats of combustion.
Chemical Equations
The chemical equations used in the problem include:
- The combustion of methanol: \[\mathrm{CH}_{3}\mathrm{OH}(l)+\frac{3}{2} \mathrm{O}_{2}(g) \rightarrow \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(l)\] \[\Delta H_{\mathrm{rxn}}^{\circ}=-726.4 \, \text{kJ/mol}\]
Another equation represents the combustion of graphite to form carbon dioxide:
- \(\mathrm{C(\text{graphite})}+\mathrm{O}_{2}(g) \rightarrow \mathrm{CO}_{2}(g) \) \[\Delta H_{\mathrm{rxn}}^{\circ}=-393.5 \, \text{kJ/mol}\]
Finally, the formation of water from hydrogen indicates the exothermic nature of this reaction:
- \(\mathrm{H}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \rightarrow \mathrm{H}_{2} \mathrm{O}(l) \) \[\Delta H_{\mathrm{rxn}}^{\circ}=-285.8 \, \text{kJ/mol}\]
Standard Enthalpy Change
When discussing standard enthalpy change, it is crucial to remember that it is defined per mole of reaction as described by a balanced equation. This property is especially useful for calculating changes involved in formation reactions, such as forming one mole of a compound from its constituent elements in their standard states.
In the given problem, we aim to calculate the standard enthalpy of formation of methanol using the provided heats of combustion. Hess's Law allows us to exploit the additive nature of enthalpy to rearrange given equations into our target equation:
- Combustion of methanol to yield carbon dioxide and water with the associated enthalpy change: \( \Delta H = -726.4 \, \text{kJ/mol}\)
- Combustion of graphite to produce carbon dioxide: \( \Delta H = -393.5 \, \text{kJ/mol}\)
- Formation of water from hydrogen: \( \Delta H = -285.8 \, \text{kJ/mol}\)