/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 51 Enthalpy changes for the followi... [FREE SOLUTION] | 91Ó°ÊÓ

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Enthalpy changes for the following reactions can be determined experimentally: \(\mathrm{N}_{2}(\mathrm{g})+3 \mathrm{H}_{2}(\mathrm{g}) \rightarrow 2 \mathrm{NH}_{3}(\mathrm{g})\) $$ \Delta_{r} H^{\circ}=-91.8 \mathrm{kJ} / \mathrm{mol}-\mathrm{rxn} $$ \(4 \mathrm{NH}_{3}(\mathrm{g})+5 \mathrm{O}_{2}(\mathrm{g}) \rightarrow 4 \mathrm{NO}(\mathrm{g})+6 \mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) $$ \Delta_{\mathrm{r}} H^{\circ}=-906.2 \mathrm{kJ} / \mathrm{mol}-\mathrm{rxn} $$ \(\mathrm{H}_{2}(\mathrm{g})+1 / 2 \mathrm{O}_{2}(\mathrm{g}) \rightarrow \mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) $$ \Delta_{i} H^{\circ}=-241.8 \mathrm{kJ} / \mathrm{mol}-\mathrm{v} \mathrm{xn} $$ Use these values to determine the enthalpy change for the formation of \(\mathrm{NO}(\mathrm{g})\) from the elements (an enthalpy change that cannot be measured directly because the reaction is reactant-favored). $$ ^{1 / 2} \mathrm{N}_{2}(\mathrm{g})+1 / 2 \mathrm{O}_{2}(\mathrm{g}) \rightarrow \mathrm{NO}(\mathrm{g}) \quad \Delta_{r} H^{\circ}=? $$

Short Answer

Expert verified
The enthalpy change for the formation of \( \mathrm{NO}(\mathrm{g}) \) from elements is \(-21.775 \mathrm{kJ/mol}\).

Step by step solution

01

Write the Target Reaction

The target reaction is \( \frac{1}{2} \mathrm{N}_{2}(\mathrm{g}) + \frac{1}{2} \mathrm{O}_{2}(\mathrm{g}) \rightarrow \mathrm{NO}(\mathrm{g}) \). Our goal is to find \( \Delta_{r} H^{\circ} \) for this reaction using the provided reactions.
02

Analyze the Given Reactions

We have three reactions: 1. \( \mathrm{N}_{2}(\mathrm{g})+3 \mathrm{H}_{2}(\mathrm{g}) \rightarrow 2 \mathrm{NH}_{3}(\mathrm{g}) \) with \( \Delta_{r} H^{\circ} = -91.8 \mathrm{kJ/mol-rxn} \).2. \( 4 \mathrm{NH}_{3}(\mathrm{g})+5 \mathrm{O}_{2}(\mathrm{g}) \rightarrow 4 \mathrm{NO}(\mathrm{g})+6 \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \) with \( \Delta_{r} H^{\circ} = -906.2 \mathrm{kJ/mol-rxn} \).3. \( \mathrm{H}_{2}(\mathrm{g})+\frac{1}{2} \mathrm{O}_{2}(\mathrm{g}) \rightarrow \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \) with \( \Delta_{i} H^{\circ} = -241.8 \mathrm{kJ/mol-rev} \).
03

Adjust Given Reactions to Form the Target Reaction

First, note that we need \( \mathrm{NO} \) on the product side. From Reaction 2, we have 4 \( \mathrm{NO} \) formed. We need to adjust this to obtain \( \frac{1}{2} \mathrm{NO} \), so divide the entire Reaction 2 by 8.This gives:\[ \mathrm{NH}_{3}(\mathrm{g}) + \frac{5}{8} \mathrm{O}_{2}(\mathrm{g}) \rightarrow \mathrm{NO}(\mathrm{g}) + \frac{3}{2} \mathrm{H}_{2}\mathrm{O}(\mathrm{g}) \]Divide the reaction enthalpy by 8: \(-\frac{906.2}{8} = -113.275 \mathrm{kJ/mol-rxn}\).
04

Add Up Adjusted Reactions to Solve for Target

Now, for each \( \mathrm{NO} \) produced, you need \( \frac{1}{2} \mathrm{N}_{2} \) and \( \frac{1}{2} \mathrm{O}_{2} \). Notice that \( \frac{1}{2} \mathrm{N}_{2} \) is produced from Reaction 1 when 1 mole of \( \mathrm{NH}_{3} \) is used. Therefore, use Reaction 3, which provides \( \mathrm{H}_{2} \mathrm{O} \), independent of the \( \mathrm{NO} \) process and it correlates with forming water.However, by rearranging, based on combined reaction:\[ \frac{1}{2} \mathrm{N}_{2} \rightarrow \mathrm{NH}_{3} \quad \Delta H_{eff1} = -91.8/3 \; (-30.6 \mathrm{kJ/mol-rxn})\]Sum to achieve:\[ \frac{1}{2} \mathrm{N}_{2} + \frac{1}{2} \mathrm{O}_{2} \rightarrow \mathrm{NO} \quad \Delta_{r} H^{\circ} = 30.6 + (-113.275) + \left(3\left(-241.8/2\right)\right) \]Evaluate, knowing the hypothetical, subtraction:\[\quad 90\; (since\ terms\ cancel) \; -113.275 = -21.775\].
05

Solve for Final Enthalpy Change

By adding the adjusted reaction enthalpies, the final enthalpy change for \( \frac{1}{2} \mathrm{N}_{2} + \frac{1}{2} \mathrm{O}_{2} \rightarrow \mathrm{NO} \) gives:\[ \Delta_{r} H^{\circ} = -21.775 \mathrm{kJ/mol} \] this results from net reducing terms and problem solution verification.

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Key Concepts

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

Thermochemistry
Thermochemistry is the study of energy transformations during chemical reactions. It's all about understanding how heat is absorbed or released when substances interact. This energy change is usually measured in terms of enthalpy (\( H \)), which represents the total heat content of a system.
In a chemical reaction, the enthalpy change (\( \Delta H \)) tells us whether the reaction is endothermic (absorbing heat) or exothermic (releasing heat).
  • **Exothermic reactions** release energy, shown by a negative \( \Delta H \). This means the products have lower energy than the reactants.
  • **Endothermic reactions** absorb energy, resulting in a positive \( \Delta H \). Here, the products have higher energy than the reactants.
Understanding these concepts helps in predicting reaction behavior and managing them in industrial processes, where energy exchange is crucial.
Hess's Law
Hess's Law is a principle in chemistry used to calculate enthalpy changes in a way that is practical when direct measurement isn't possible. According to Hess's Law, if a chemical reaction is expressed as a series of steps, the overall enthalpy change is equal to the sum of the enthalpy changes for each step.
This law is extremely useful for calculating enthalpy changes for reactions that are difficult to measure directly, such as the formation of reactive or unstable compounds. For our exercise, we used Hess's Law to find the enthalpy change for the formation of \( \text{NO} \) gas by manipulating given reactions.
  • **Key Insight**: The path taken to reach the final reaction does not affect the overall enthalpy change.
  • **Application**: Simply add up the enthalpy changes of the individual steps to find the overall change.
Understanding and applying Hess's Law provides flexibility in chemistry, allowing predictions of reaction energetics without direct experimentation.
Chemical Reactions
Chemical reactions involve the reorganization of atoms and are described by chemical equations. The focus of thermochemistry in reactions is to understand how these atomic changes correlate with energy changes.
In our exercise, several reactions were considered:
  • Combining nitrogen and hydrogen to form ammonia shows an exothermic process.
  • Burning ammonia in oxygen results in the formation of nitrogen monoxide and water.
  • Forming water from hydrogen and oxygen is another exothermic process.
Balancing such equations ensures that the law of conservation of mass is obeyed, meaning that atoms are neither created nor destroyed.
  • **Reactants and Products**: Reactions start with reactants and end with products, and keeping track of \( \Delta H \) helps in understanding the energy landscape of these transformations.
  • **Stoichiometry**: Correct stoichiometric coefficients ensure the right pathway to calculate enthalpy changes with Hess's Law.
By understanding these basics, you can predict not just the quantities of substances involved in reactions but also the energy transformations accompanying these changes.

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Most popular questions from this chapter

Energy: Some Basic Principles Define the terms system and surroundings. What does it mean to say that a system and its surroundings are in thermal equilibrium?

An "ice calorimeter" can be used to determine the specific heat capacity of a metal. A piece of hot metal is dropped onto a weighed quantity of ice. The energy transferred from the metal to the ice can be determined from the amount of ice melted. Suppose you heated a 50.0 -g piece of silver to \(99.8^{\circ} \mathrm{C}\) and then dropped it onto ice. When the metal's temperature had dropped to \(0.0^{\circ} \mathrm{C},\) it is found that \(3.54 \mathrm{g}\) of ice had melted. What is the specific heat capacity of silver?

A The standard molar enthalpy of formation of diborane, \(\mathrm{B}_{2} \mathrm{H}_{6}(\mathrm{g}),\) cannot be determined directly because the compound cannot be prepared by the reaction of boron and hydrogen. It can be calculated from other enthalpy changes, however. The following enthalpy changes can be measured. \(4 \mathrm{B}(\mathrm{s})+3 \mathrm{O}_{2}(\mathrm{g}) \rightarrow 2 \mathrm{B}_{2} \mathrm{O}_{3}(\mathrm{s})\) \(\Delta_{1} H^{\circ}=-2543.8 \mathrm{kJ} / \mathrm{mol}-\mathrm{pxn}\) \(\mathrm{H}_{2}(\mathrm{g})+^{1 / 2} \mathrm{O}_{2}(\mathrm{g}) \rightarrow \mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) \(\Delta_{r} H^{\prime \prime}=-241.8 \mathrm{kJ} / \mathrm{mol}-\mathrm{rxn}\) \(\mathrm{B}_{2} \mathrm{H}_{6}(\mathrm{g})+3 \mathrm{O}_{2}(\mathrm{g}) \rightarrow \mathrm{B}_{2} \mathrm{O}_{3}(\mathrm{s})+3 \mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) \(\Delta_{\tau} H^{\circ}=-2032.9 \mathrm{kJ} / \mathrm{mol}-\mathrm{rxn}\) (a) Show how these equations can be added together to give the equation for the formation of \(\mathrm{B}_{2} \mathrm{H}_{6}(\mathrm{g})\) from \(\mathrm{B}(\mathrm{s})\) and \(\mathrm{H}_{2}(\mathrm{g})\) in their standard states. Assign enthalpy changes to each reaction. (b) Calculate \(\Delta_{f} H^{\circ}\) for \(\mathrm{B}_{2} \mathrm{H}_{6}(\mathrm{g})\) (c) Draw an energy level diagram that shows how the various enthalpies in this problem are related. (d) Is the formation of \(\mathrm{B}_{2} \mathrm{H}_{6}(\mathrm{g})\) from its elements exo-or endothermic?

According to the Nutrient Data Laboratory website (www, ars. usda.gov/ba/bhnrc/ndl), corn oil contains \(3766 \mathrm{kJ}\) of energy per \(100 .\) g serving. (a) What is the energy content of \(100 .\) g of corn oil in units of nutritional calories (Cal)? (b) How many tablespoons of corn oil have an energy content equivalent to 1500 nutritional calories? (1.0 Tbsp \(=14\) g of corn oil) (c) What mass of water can be heated from \(25.0^{\circ} \mathrm{C}\) to its boiling point of \(100.0^{\circ}\) C using the energy of combustion of 1.00 Tbsp of corn oil?

You should use care when dissolving \(\mathrm{H}_{2} \mathrm{SO}_{4}\) in water because the process is highly exothermic. To measure the enthalpy change, \(5.2 \mathrm{g}\) of concentrated \(\mathrm{H}_{2} \mathrm{SO}_{4}(\ell)\) was added (with stirring) to 135 g of water in a coffee-cup calorimeter. This resulted in an increase in temperature from \(20.2^{\circ} \mathrm{C}\) to \(28.8^{\circ} \mathrm{C} .\) Calculate the enthalpy change for the process \(\mathrm{H}_{2} \mathrm{SO}_{4}(\ell) \rightarrow \mathrm{H}_{2} \mathrm{SO}_{4}(\mathrm{aq}),\) in kJ/mol.

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