Calculate the standard enthalpy change for the reaction $$ 2 \mathrm{Al}(s)+\mathrm{Fe}_{2} \mathrm{O}_{3}(s) \longrightarrow 2 \mathrm{Fe}(s)+\mathrm{Al}_{2} \mathrm{O}_{3}(s) $$ given that $$ \begin{aligned} 2 \mathrm{Al}(s)+\frac{3}{2} \mathrm{O}_{2}(g) \longrightarrow & \mathrm{Al}_{2} \mathrm{O}_{3}(s) \\ \Delta H_{\mathrm{rxn}}^{\circ} &=-1669.8 \mathrm{~kJ} / \mathrm{mol} \\ 2 \mathrm{Fe}(s)+\frac{3}{2} \mathrm{O}_{2}(g) \longrightarrow & \mathrm{Fe}_{2} \mathrm{O}_{3}(s) \\ \Delta H_{\mathrm{rxn}}^{\circ} &=-822.2 \mathrm{~kJ} / \mathrm{mol} \end{aligned} $$

Short Answer

Expert verified
847.6 kJ/mol

Step by step solution

01

Formulate the equation

Firstly, it's necessary to analyze closely the given reactions and the required reaction. The main aim here is to adjust the given reactions such that when combined, can give the desired reaction. Here, the first given reaction needs to be reversed and the second given reaction kept as is to achieve the required reaction.
02

Apply Hess's Law

According to Hess's law, the enthalpy change of the overall process equals the sum of enthalpy changes of its individual steps. So, once the equations are flipped or multiplied to match with the final reaction, do the same with their respective standard enthalpies.
03

Calculate the standard enthalpy change

Now the enthalpies could be summed up to get the standard enthalpy change for the desired reaction. The new enthalpy change for the 1st reaction after being reversed will be its negative, therefore, \( \Delta H_{1}^{\circ} = 1669.8 \mathrm{~kJ} / \mathrm{mol} \). Keeping the second reaction and its enthalpy change as it is; \( \Delta H_{2}^{\circ} = -822.2 \mathrm{~kJ} / \mathrm{mol}\). Adding these two will give the enthalpy change for the given reaction: \( \Delta H_{\mathrm{rxn}}^{\circ} = \Delta H_{1}^{\circ} + \Delta H_{2}^{\circ}\).
04

Result

Now substitute the values from step 3 in the above equation. So the final calculation will be \( \Delta H_{\mathrm{rxn}}^{\circ} = 1669.8-822.2 \mathrm{~kJ} / \mathrm{mol}\)

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Key Concepts

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

Hess's Law
Understanding Hess's Law in thermochemistry is crucial when it comes to determining the enthalpy change of a chemical reaction that is not directly measurable. The enthalpy of a reaction depends solely upon the initial and final states of the system and not on the path taken. This principle is famously encapsulated in Hess's Law, which states that the total enthalpy change for a chemical reaction is the same, regardless of the number of steps taken to perform the reaction.

Hess's Law makes it possible to calculate the enthalpy changes for complex chemical reactions by breaking them down into a series of simpler steps with known enthalpy changes. To apply this law, equations representing individual steps of a reaction are manipulated — reversed or multiplied to match the number of moles with those in the final reaction — and their respective enthalpy changes are adjusted accordingly. The overall enthalpy change is then obtained by summing the enthalpy changes for each step.

By using Hess's Law, we can apply known thermochemical equations to find the enthalpy change of the main reaction, much like completing a puzzle with pieces representing simpler reactions. In essence, Hess's Law serves as a bookkeeping tool, allowing for the balance of energy changes just as one would balance atoms in a chemical equation.
Thermochemistry
Thermochemistry is the branch of chemistry that deals with the study of the heat energy involved in chemical reactions and physical transformations. The central concept in thermochemistry is the enthalpy change, often symbolized as \(\Delta H\). It's a measure of the heat change at constant pressure and is expressed in units of kilojoules per mole (kJ/mol).

Every chemical reaction either absorbs or releases energy in the form of heat, leading to two primary classifications of reactions:
  • Endothermic reactions: These absorb heat, resulting in a positive \(\Delta H\).
  • Exothermic reactions: These release heat, resulting in a negative \(\Delta H\).

Understanding the energetics of chemical reactions is fundamental to various applications in science and engineering, such as designing batteries, understanding metabolism in living organisms, and predicting the impacts of reactions on the environment.
Enthalpy of Reaction
The enthalpy of reaction, or reaction enthalpy, is the heat change that occurs during a reaction at constant pressure and is represented by the symbol \(\Delta H_{\text{rxn}}^\circ\). It is an essential quantity in the study of chemical reactions, as it provides insight into the energetics and spontaneity of the process. When the reaction releases heat, the enthalpy of reaction is negative, indicating it is exothermic. Conversely, if heat is absorbed, the enthalpy of reaction is positive, suggesting an endothermic nature.

The standard enthalpy change \(\Delta H^\circ\) refers to the enthalpy change when all reactants and products are in their standard states, usually at 1 bar of pressure. Standard enthalpy changes provide a reference point to compare the relative energetics of different reactions and are fundamental when applying Hess's Law, as shown in our original exercise.

To calculate the standard enthalpy change, it's important to ensure that the stoichiometry of the reactions matches the overall process being analyzed. The steps provided in our textbook solution illustrate the method to obtain the enthalpy change for the desired reaction, often using tabulated values of standard enthalpy changes for individual reactions or formation enthalpies of compounds.

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Most popular questions from this chapter

A 44.0-g sample of an unknown metal at \(99.0^{\circ} \mathrm{C}\) was placed in a constant-pressure calorimeter containing \(80.0 \mathrm{~g}\) of water at \(24.0^{\circ} \mathrm{C}\). The final temperature of the system was found to be \(28.4^{\circ} \mathrm{C}\). Calculate the specific heat of the metal. (The heat capacity of the calorimeter is \(\left.12.4 \mathrm{~J} /{ }^{\circ} \mathrm{C} .\right)\)

Lime is a term that includes calcium oxide \((\mathrm{CaO}\) also called quicklime) and calcium hydroxide \(\left[\mathrm{Ca}(\mathrm{OH})_{2},\right.\) also called slaked lime \(] .\) It is used in the steel industry to remove acidic impurities, in airpollution control to remove acidic oxides such as \(\mathrm{SO}_{2}\), and in water treatment. Quicklime is made industrially by heating limestone \(\left(\mathrm{CaCO}_{3}\right)\) above \(2000^{\circ} \mathrm{C}\) : $$ \begin{aligned} \mathrm{CaCO}_{3}(s) \longrightarrow \mathrm{CaO}(s)+\mathrm{CO}_{2}(g) \\ \Delta H^{\circ} &=177.8 \mathrm{~kJ} / \mathrm{mol} \end{aligned} $$ Slaked lime is produced by treating quicklime with water: $$ \begin{aligned} \mathrm{CaO}(s)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{Ca}(\mathrm{OH})_{2}(s) \\ \Delta H^{\circ} &=-65.2 \mathrm{~kJ} / \mathrm{mol} \end{aligned} $$ The exothermic reaction of quicklime with water and the rather small specific heats of both quicklime \(\left(0.946 \mathrm{~J} / \mathrm{g} \cdot{ }^{\circ} \mathrm{C}\right)\) and slaked lime \(\left(1.20 \mathrm{~J} / \mathrm{g} \cdot{ }^{\circ} \mathrm{C}\right)\) make it hazardous to store and transport lime in vessels made of wood. Wooden sailing ships carrying lime would occasionally catch fire when water leaked into the hold. (a) If a 500 -g sample of water reacts with an equimolar amount of \(\mathrm{CaO}\) (both at an initial temperature of \(\left.25^{\circ} \mathrm{C}\right)\), what is the final temperature of the product, \(\mathrm{Ca}(\mathrm{OH})_{2} ?\) Assume that the product absorbs all of the heat released in the reaction. (b) Given that the standard enthalpies of formation of \(\mathrm{CaO}\) and \(\mathrm{H}_{2} \mathrm{O}\) are \(-635.6 \mathrm{~kJ} / \mathrm{mol}\) and \(-285.8 \mathrm{~kJ} / \mathrm{mol}\), respectively, cal- culate the standard enthalpy of formation of \(\mathrm{Ca}(\mathrm{OH})_{2}\).

State Hess's law. Explain, with one example, the usefulness of Hess's law in thermochemistry.

Which of the following standard enthalpy of formation values is not zero at \(25^{\circ} \mathrm{C} ? \mathrm{Na}(s), \mathrm{Ne}(g)\) \(\mathrm{CH}_{4}(g), \mathrm{S}_{8}(s), \mathrm{Hg}(l), \mathrm{H}(g)\)

The internal energy of an ideal gas depends only on its temperature. Do a first-law analysis of this process. A sample of an ideal gas is allowed to expand at constant temperature against atmospheric pressure. (a) Does the gas do work on its surroundings? (b) Is there heat exchange between the system and the surroundings? If so, in which direction? (c) What is \(\Delta E\) for the gas for this process?

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