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Complete combustion of 1 mol of acetone \(\left(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}\right)\) liberates \(1790 \mathrm{kJ} :\) $$\begin{aligned} \mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O}(l)+4 \mathrm{O}_{2}(g) \longrightarrow & 3 \mathrm{CO}_{2}(g)+3 \mathrm{H}_{2} \mathrm{O}(l) \\ & \quad \quad \quad \quad \quad \quad \quad \Delta H^{\circ}=-1790 \mathrm{kJ} \end{aligned}$$ Using this information together with the standard enthalpies of formation of \(\mathrm{O}_{2}(g), \mathrm{CO}_{2}(g),\) and \(\mathrm{H}_{2} \mathrm{O}(l)\) from Appendix \(\mathrm{C},\) calculate the standard enthalpy of formation of acetone.

Short Answer

Expert verified
The standard enthalpy of formation of acetone is -1380.9 kJ/mol.

Step by step solution

01

Write the equations for the standard enthalpies of formation

The standard enthalpies of formation are the enthalpies required to form 1 mol of a substance from its elements in their standard states. The equation for the formation of acetone is: \(C(s) + 3H_2(g) + \frac{1}{2}O_2(g) \to C_{3}H_{6}O(l)\) The equations for the formation of CO2 and H2O are: \(C(s) + O_2(g) \to CO_{2}(g)\) \(H_2(g) + \frac{1}{2}O_2(g) \to H_{2}O(l)\)
02

Determine the ∆H°f for CO2 and H2O

The standard enthalpies of formation for CO2(g) and H2O(l) can be found in Appendix C. Using this information, we have: ∆H°f(CO2(g))=-393.5 kJ/mol ∆H°f(H2O(l))=-285.8 kJ/mol
03

Set up the Hess's Law equation

Hess's Law states that the total enthalpy change for a reaction is the sum of the individual enthalpy changes for each step in the reaction. For the given problem, we can write the Hess's Law equation using the balanced equation of acetone combustion and the standard enthalpies of formation, as follows: \(\Delta H_{combustion}^{°} = 3\Delta H_{f(CO2(g))}^° + 3\Delta H_{f(H2O(l))^° − (\Delta H_{f(acetone)}^° + 4\Delta H_{f(O2(g))}^°)\) We know that, for O2(g), ∆H°f = 0 kJ/mol, since it is an element in its standard state. So we can simplify the equation: \(\Delta H_{combustion}^{°} = 3\Delta H_{f(CO2(g))}^° + 3\Delta H_{f(H2O(l))^° − \Delta H_{f(acetone)}^°\)
04

Calculate the ∆H°f of acetone

Now, plug in the known values and solve for the standard enthalpy of formation of acetone: \(-1790 kJ/mol = 3(-393.5 kJ/mol) + 3(-285.8 kJ/mol) – \Delta H_{f(acetone)}^°\) Solve the equation for ∆H°f(acetone): \(\Delta H_{f(acetone)}^° = 3(-393.5 kJ/mol) + 3(-285.8 kJ/mol) + 1790 kJ/mol\) \(\Delta H_{f(acetone)}^° = -1380.9 kJ/mol\) So, the standard enthalpy of formation of acetone is -1380.9 kJ/mol.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Hess's Law
Hess's Law is a key principle in thermochemistry. It states that the total enthalpy change for a chemical reaction is the same, no matter how it is carried out, in one step or multiple steps. This means that we can calculate the enthalpy change for a complex reaction by breaking it down into a series of simpler steps for which enthalpy changes are known.

Here's how it works in practice:
  • Identify the initial and final states of the reaction.
  • Break the reaction into multiple steps.
  • Use known enthalpy changes for these steps to find the total enthalpy change.
In our exercise, we used Hess's Law by writing an equation that combined the enthalpy changes for the formation of carbon dioxide and water and related them to the combustion of acetone. This allowed us to find the enthalpy change for forming acetone from its elements.
Combustion Reaction
A combustion reaction occurs when a substance reacts quickly with oxygen, releasing energy in the form of heat or light. This energy release often makes combustion reactions very exothermic and noticeable.

In the context of our exercise:
  • The combustion of acetone involves reacting with oxygen to produce carbon dioxide and water.
  • The reaction is highly exothermic, releasing 1790 kJ of energy.
  • Combustion reactions are important in energy production, like in engines and fires.
Understanding the energy changes in combustion reactions helps us calculate unknown values, like the standard enthalpy of formation, using known data.
Standard Enthalpies
Standard enthalpies of formation (\( \Delta H_{f}^{\circ} \)) are defined as the enthalpy change when one mole of a compound is formed from its elements in their standard states. These values are crucial in calculating the overall enthalpy change of reactions using known enthalpy changes.

Key points include:
  • Elements in their standard states have a formation enthalpy of zero.
  • Standard enthalpies are usually measured under conditions of 1 atm and 25°C (298 K).
  • These values help us use Hess's Law effectively to calculate unknown enthalpies, like in the acetone example.
In our exercise, we used the standard enthalpies of CO2 and H2O to deduce the enthalpy of formation for acetone, tying all these concepts together into a clear calculation.

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Most popular questions from this chapter

Ozone, \(\mathrm{O}_{3}(g),\) is a form of elemental oxygen that plays an important role in the absorption of ultraviolet radiation in the stratosphere. It decomposes to \(\mathrm{O}_{2}(g)\) at room temperature and pressure according to the following reaction: $$2 \mathrm{O}_{3}(g) \longrightarrow 3 \mathrm{O}_{2}(g) \quad \Delta H=-284.6 \mathrm{kJ}$$ (a) What is the enthalpy change for this reaction per mole of \(\mathrm{O}_{3}(g) ?\) (b) Which has the higher enthalpy under these conditions, 2 \(\mathrm{O}_{3}(g)\) or 3 \(\mathrm{O}_{2}(g) ?\)

(a) When a 4.25 -g sample of solid ammonium nitrate dissolves in 60.0 g of water in a coffee-cup calorimeter (Figure 5.18), the temperature drops from 22.0 to \(16.9^{\circ} \mathrm{C}\) . Calculate \(\Delta H\left(\) in \(\mathrm{kJ} / \mathrm{mol} \mathrm{NH}_{4} \mathrm{NO}_{3}\right)\) for the solution process: $$\mathrm{NH}_{4} \mathrm{NO}_{3}(s) \longrightarrow \mathrm{NH}_{4}^{+}(a q)+\mathrm{NO}_{3}^{-}(a q)$$ Assume that the specific heat of the solution is the same as that of pure water. (b) Is this process endothermic or exothermic?

Consider the combustion of liquid methanol, \(\mathrm{CH}_{3} \mathrm{OH}(l) :\) $$\begin{aligned} \mathrm{CH}_{3} \mathrm{OH}(l)+\frac{3}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(l) & \\ \Delta H &=-726.5 \mathrm{kJ} \end{aligned}$$ (a) What is the enthalpy change for the reverse reaction? (b) Balance the forward reaction with whole-number coefficients. What is \(\Delta H\) for the reaction represented by this equation? (c) Which is more likely to be thermodynamically favored, the forward reaction or the reverse reaction? (d) If the reaction were written to produce \(\mathrm{H}_{2} \mathrm{O}(g)\) instead of \(\mathrm{H}_{2} \mathrm{O}(l),\) would you expect the magnitude of \(\Delta H\) to increase, decrease, or stay the same? Explain.

Write balanced equations that describe the formation of the following compounds from elements in their standard states, and then look up the standard enthalpy of formation for each substance in Appendix C: (a) \(\mathrm{H}_{2} \mathrm{O}_{2}(g),(\mathbf{b}) \mathrm{CaCO}_{3}(s)\) (c) \(\mathrm{POCl}_{3}(l),(\mathbf{d}) \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l) .\)

(a) What is the value of the standard enthalpy of formation of an element in its most stable form? (b) Write the chemical equation for the reaction whose enthalpy change is the standard enthalpy of formation of sucrose (table sugar), \(\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}(s), \Delta H_{f}^{\circ}\left[\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}(s)\right]\)

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