Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

From the enthalpies of reaction \(\begin{aligned} 2 \mathrm{H}_{2}(g)+\mathrm{O}_{2}(g) & \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}(g) & \Delta H &=-483.6 \mathrm{~kJ} \\ 3 \mathrm{O}_{2}(g) & \cdots &-\cdots & 2 \mathrm{O}_{3}(g) & \Delta H &=+284.6 \mathrm{~kJ} \end{aligned}\) calculate the heat of the reaction $$ 3 \mathrm{H}_{2}(\mathrm{~g})+\mathrm{O}_{3}(\mathrm{~g}) \longrightarrow 3 \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) $$

Short Answer

Expert verified
The heat of the reaction for \(3 \mathrm{H}_{2}(g)+\mathrm{O}_{3}(g) \longrightarrow 3\mathrm{H}_{2}\mathrm{O}(g)\) is \(-583.1 \mathrm{kJ}\).

Step by step solution

01

Write the target reaction

The target reaction we need to calculate the heat of is: $$ 3 \mathrm{H}_{2}(g)+\mathrm{O}_{3}(g) \longrightarrow 3\mathrm{H}_{2}\mathrm{O}(g) $$
02

Analyze the given reactions

We are given two reactions with their enthalpy changes: $$ 2 \mathrm{H}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2\mathrm{H}_{2}\mathrm{O}(g) \qquad \Delta H_1=-483.6 \mathrm{kj} $$ $$ 3\mathrm{O}_{2}(g) \longrightarrow 2\mathrm{O}_{3}(g) \qquad \Delta H_2=+284.6 \mathrm{kJ} $$
03

Manipulate the given reactions to match the target reaction

In order to apply Hess's Law, we must manipulate the given reactions so that they sum to the target reaction: 1. Multiply the first reaction by 3/2 to get 3 moles of water on the product side: $$ 3 \mathrm{H}_{2}(g) + \frac{3}{2}\mathrm{O}_{2}(g) \longrightarrow 3\mathrm{H}_{2}\mathrm{O}(g) \qquad \Delta H_1'= 3/2(-483.6) \mathrm{kJ} $$ 2. Divide the second reaction by 2 to obtain 1 mole of ozone in the reactant side: $$ \frac{3}{2}\mathrm{O}_{2}(g) \longrightarrow \mathrm{O}_{3}(g) \qquad \Delta H_2'= 1/2(+284.6) \mathrm{kJ} $$
04

Apply Hess's Law

Now that the reactions have been manipulated, we can sum them up to get the target reaction: $$ 3 \mathrm{H}_{2}(g)+\mathrm{O}_{3}(g) \longrightarrow 3\mathrm{H}_{2}\mathrm{O}(g) $$ Applying Hess's Law, we add the enthalpy changes of the manipulated reactions to find the enthalpy change of the target reaction: $$ \Delta H_{target} = \Delta H_1' + \Delta H_2' = 3/2(-483.6 \mathrm{kJ}) + 1/2(+284.6 \mathrm{kJ}) $$
05

Calculate the enthalpy of the target reaction

Finally, we calculate the enthalpy change of the target reaction: $$ \Delta H_{target} =-725.4 \mathrm{kJ} + 142.3 \mathrm{kJ} = -583.1\mathrm{kJ} $$ The heat of the reaction is -583.1 kJ.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

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

Enthalpy Change
Enthalpy change, represented with the symbol \( \Delta H \), is a measure of heat energy released or absorbed when a chemical reaction takes place at constant pressure. Understanding this concept is fundamental to grasping chemical reactions, as it indicates whether a process is endothermic (heat absorbed, \( \Delta H > 0 \) or exothermic (heat released, \( \Delta H < 0 \).

In the given exercise, the enthalpy change of a reaction transforming hydrogen gas and ozone into water vapor is calculated using given enthalpy values for related reactions. The key aspect to discern here is that the enthalpy is a state function, meaning its value depends only on the initial and final states of a system, not on the path taken.

By understanding and working with enthalpy changes, students can predict the heat released or absorbed during reactions, which is critical in both academic studies and real-world applications like energy production and material synthesis.
Chemical Thermodynamics
Chemical thermodynamics is the branch of chemistry that deals with the energy changes accompanying chemical reactions and physical processes. It provides tools to predict whether processes are feasible under given conditions and to understand how systems reach equilibrium.

Hess's Law, an application of the first law of thermodynamics, is instrumental in chemical thermodynamics. It states that the total enthalpy change for a chemical reaction is the same, regardless of the number of stages in which the reaction is carried out. As seen in our exercise, we utilized Hess's Law to find the enthalpy change of a complex reaction by combining simpler reactions whose enthalpy changes are known.

For students, mastering chemical thermodynamics means getting comfortable with concepts such as enthalpy, entropy, and Gibbs free energy, which together describe the energy changes and spontaneity of reactions.
Enthalpies of Reaction
Enthalpies of reaction refer to the amount of heat absorbed or released by a system during a chemical reaction at constant pressure. Each chemical equation has an associated enthalpy change, which can be either positive or negative depending on whether the reaction is endothermic or exothermic.

The balancing of equations in a manner that reflects the conservation of mass and the use of stoichiometry are important when working with enthalpies of reaction, as seen in the exercise. Manipulating the given reactions properly to have the correct stoichiometry, thus allowing the application of Hess's Law, was critical. Each adjusted reaction represented steps contributing to the overall reaction, and their individual enthalpies were combined accurately to give the enthalpy of the desired reaction.

This understanding aids in many practical applications, such as calculating energy requirements for industrial chemical processes and designing reactions for new materials.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

The specific heat of ethylene glycol is \(2.42 \mathrm{~J} / \mathrm{g}-\mathrm{K} .\) How many J of heat are needed to raise the temperature of \(62.0 \mathrm{~g}\) of ethylene glycol from \(13.1^{\circ} \mathrm{C}\) to \(40.5^{\circ} \mathrm{C}\) ?

The complete combustion of acetic acid, \(\mathrm{CH}_{3} \mathrm{COOH}(l)\), to form \(\mathrm{H}_{2} \mathrm{O}(l)\) and \(\mathrm{CO}_{2}(g)\) at constant pressure releases \(871.7 \mathrm{~kJ}\) of heat per mole of \(\mathrm{CH}_{3} \mathrm{COOH}\). (a) Write a balanced thermochemical equation for this reaction. (b) Draw an enthalpy diagram for the reaction.

You are given \(\Delta H\) for a process that occurs at constant pressure. What additional information do you need to determine \(\Delta E\) for the process?

Consider the decomposition of liquid benzene, \(\mathrm{C}_{6} \mathrm{H}_{6}(l)\), to gaseous acetylene, \(\mathrm{C}_{2} \mathrm{H}_{2}(\mathrm{~g})\) : $$ \mathrm{C}_{6} \mathrm{H}_{6}(l) \longrightarrow 3 \mathrm{C}_{2} \mathrm{H}_{2}(g) \quad \Delta H=+630 \mathrm{~kJ} $$ (a) What is the enthalpy change for the reverse reaction? (b) What is \(\Delta H\) for the formation of \(1 \mathrm{~mol}\) of acetylene? (c) Which is more likely to be thermodynamically favored, the forward reaction or the reverse reaction? (d) If \(C_{6} \mathrm{H}_{6}(g)\) were consumed instead of \(\mathrm{C}_{6} \mathrm{H}_{6}(l)\), would you expect the magnitude of \(\Delta H\) to increase, decrease, or stay the same? Explain.

From the enthalpies of reaction calculate \(\Delta H\) for the reaction of ethylene with \(\mathrm{F}_{2}\) $$ \mathrm{C}_{2} \mathrm{H}_{4}(g)+6 \mathrm{~F}_{2}(g)-\cdots 2 \mathrm{CF}_{4}(g)+4 \mathrm{HF}(g) $$

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free