Calculate the enthalpy change for the reaction $$ \mathrm{P}_{4} \mathrm{O}_{6}(s)+2 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) $$ given the following enthalpies of reaction: $$ \begin{array}{ll} \mathrm{P}_{4}(s)+3 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{6}(s) & \Delta H=-1640.1 \mathrm{~kJ} \\ \mathrm{P}_{4}(s)+5 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) & \Delta H=-2940.1 \mathrm{~kJ} \end{array} $$

Short Answer

Expert verified
The enthalpy change for the given reaction, \(\mathrm{P}_{4}\mathrm{O}_{6}(s) + 2\mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4}\mathrm{O}_{10}(s)\), can be calculated by combining the given reactions and their enthalpy changes. The resulting enthalpy change for the target reaction is: $$ \Delta H_{\mathrm{overall}} = -1300\ \mathrm{kJ} $$

Step by step solution

01

Write down the given reactions and their enthalpies

We have the following reactions and their enthalpy changes: Reaction 1: $$ \mathrm{P}_{4}(s) + 3\mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4}\mathrm{O}_{6}(s) \\ \Delta H_1 = -1640.1\ \mathrm{kJ} $$ Reaction 2: $$ \mathrm{P}_{4}(s) + 5\mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4}\mathrm{O}_{10}(s) \\ \Delta H_2 = -2940.1\ \mathrm{kJ} $$ We want to calculate the enthalpy change for this reaction: $$ \mathrm{P}_{4}\mathrm{O}_{6}(s) + 2\mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4}\mathrm{O}_{10}(s) $$
02

Combine the reactions to form the target reaction

First, let's reverse Reaction 1 so that we have \(\mathrm{P}_{4}\mathrm{O}_{6}(s)\) on the reactant side: $$ \mathrm{P}_{4}\mathrm{O}_{6}(s) \longrightarrow \mathrm{P}_{4}(s) + 3\mathrm{O}_{2}(g) \\ \Delta H_1^\prime = 1640.1\ \mathrm{kJ} \qquad (\mathrm{since\ the\ reaction\ has\ been\ reversed}) $$ Now, let's add Reaction 1' and Reaction 2 together: Reaction 1': $$ \mathrm{P}_{4}\mathrm{O}_{6}(s) \longrightarrow \mathrm{P}_{4}(s) + 3\mathrm{O}_{2}(g) $$ Reaction 2: $$ \mathrm{P}_{4}(s) + 5\mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4}\mathrm{O}_{10}(s) $$ As we add the two reactions, \(\mathrm{P}_{4}(s)\) on the right of Reaction 1' cancels with \(\mathrm{P}_{4}(s)\) on the left of Reaction 2. Similarly, \(3\mathrm{O}_{2}(g)\) on the right of Reaction 1' combines with \(5\mathrm{O}_{2}(g)\) on the left of Reaction 2, resulting in \(2\mathrm{O}_{2}(g)\) on the left side of the overall reaction. Resulting overall reaction: $$ \mathrm{P}_{4}\mathrm{O}_{6}(s) + 2\mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4}\mathrm{O}_{10}(s) $$
03

Calculate the enthalpy change for the target reaction

As we add Reaction 1' and Reaction 2 to obtain the resulting overall reaction, we should also sum their enthalpy changes to obtain the enthalpy change for the target reaction. \(\Delta H_{\mathrm{overall}} = \Delta H_1^\prime + \Delta H_2 = 1640.1\ \mathrm{kJ} - 2940.1\ \mathrm{kJ} = -1300\ \mathrm{kJ}\) So, the enthalpy change for the target reaction is: $$ \Delta H_{\mathrm{overall}} = -1300\ \mathrm{kJ} $$

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!

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

A coffee-cup calorimeter of the type shown in Figure 5.18 contains $150.0 \mathrm{~g}\( of water at \)25.2^{\circ} \mathrm{C}\(. A \)200-\mathrm{g}$ block of silver metal is heated to \(100.5^{\circ} \mathrm{C}\) by putting it in a beaker of boiling water. The specific heat of \(\mathrm{Ag}(s)\) is $0.233 \mathrm{~J} /(\mathrm{g} \cdot \mathrm{K})\(. The \)\mathrm{Ag}$ is added to the calorimeter, and after some time the contents of the cup reach a constant temperature of \(30.2^{\circ} \mathrm{C} .(\mathbf{a})\) Determine the amount of heat, in J, lost by the silver block. (b) Determine the amount of heat gained by the water. The specific heat of water is $4.184 \mathrm{~J} /(\mathrm{g} \cdot \mathrm{K}) .(\mathbf{c})$ The difference between your answers for (a) and (b) is due to heat loss through the Styrofoam \(^{\circ}\) cups and the heat necessary to raise the temperature of the inner wall of the apparatus. The heat capacity of the calorimeter is the amount of heat necessary to raise the temperature of the apparatus (the cups and the stopper) by \(1 \mathrm{~K} .\) Calculate the heat capacity of the calorimeter in \(\mathrm{J} / \mathrm{K}\). (d) What would be the final temperature of the system if all the heat lost by the silver block were absorbed by the water in the calorimeter?

Suppose that the gas-phase reaction $2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow\( \)2 \mathrm{NO}_{2}(g)$ were carried out in a constant-volume container at constant temperature. (a) Would the measured heat change represent \(\Delta H\) or \(\Delta E\) ? (b) If there is a difference, which quantity is larger for this reaction? (c) Explain your answer to part (b).

Atomic hydrogen (H) is used in welding (AHW). The atoms recombine to hydrogen molecules with a large release of heat according to the following reaction: $$ 2 \mathrm{H}(g) \longrightarrow \mathrm{H}_{2}(g) $$ (a) Using the thermodynamic data in Appendix C, calculate the enthalpy change for this reaction per mole of \(\mathrm{H}_{2}\). (b) Which has the higher enthalpy under these conditions, \(2 \mathrm{H}(g)\) or \(\mathrm{H}_{2}(g) ?\)

Consider a system consisting of the following apparatus, in which gas is confined in one flask and there is a vacuum in the other flask. The flasks are separated by a valve. Assume that the flasks are perfectly insulated and will not allow the flow of heat into or out of the flasks to the surroundings. When the valve is opened, gas flows from the filled flask to the evacuated one. (a) Is work performed during the expansion of the gas? (b) Why or why not? (c) Can you determine the value of \(\Delta E\) for the process?

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) \(\mathrm{CH}_{3} \mathrm{OH}(l),\) (b) \(\mathrm{CaSO}_{4}(s),\) (d) \(\mathrm{P}_{4} \mathrm{O}_{6}(s),\) (c) \(\mathrm{NO}(g)\).

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