/*! 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 82 Given the following data $$ ... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

Given the following data $$ \begin{aligned} \mathrm{P}_{4}(s)+6 \mathrm{Cl}_{2}(g) \longrightarrow 4 \mathrm{PCl}_{3}(g) & \Delta H=-1225.6 \mathrm{kJ} \\ \mathrm{P}_{4}(s)+5 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) & \Delta H=-2967.3 \mathrm{kJ} \end{aligned} $$ $$ \begin{array}{cc}{\mathrm{PCl}_{3}(g)+\mathrm{Cl}_{2}(g) \longrightarrow \mathrm{PCl}_{5}(g)} & {\Delta H=-84.2 \mathrm{kJ}} \\\ {\mathrm{PCl}_{3}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{Cl}_{3} \mathrm{PO}(g)} & {\Delta H=-285.7 \mathrm{kJ}}\end{array} $$ calculate \(\Delta H\) for the reaction $$ \mathrm{P}_{4} \mathrm{O}_{10}(s)+6 \mathrm{PCl}_{5}(g) \longrightarrow 10 \mathrm{Cl}_{3} \mathrm{PO}(g) $$

Short Answer

Expert verified
The enthalpy change for the reaction \(\mathrm{P_{4}O_{10}(s) + 6 \mathrm{PCl}_{5}(g) \longrightarrow 10 \mathrm{Cl}_{3} \mathrm{PO}(g)\) is \(\Delta H_{target} = -4470.7 \,\mathrm{kJ}\).

Step by step solution

01

1. Identify the target reaction

The target reaction we want to find the enthalpy change for is: \( \mathrm{P}_{4} \mathrm{O}_{10}(s) + 6 \mathrm{PCl}_{5}(g) \longrightarrow 10 \mathrm{Cl}_{3} \mathrm{PO}(g) \)
02

2. Manipulate the given reactions to match the target reaction

First, let's work with the second given reaction (\( \mathrm{P}_{4}(s) + 5 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) \)), as it is the only one with the P4O10 compound. Since the target reaction begins with 1 P4O10, we keep the second reaction the same and not need to manipulate it: \( \mathrm{P}_{4}(s) + 5 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) \, (\Delta H_2 = -2967.3 \,\mathrm{kJ}) \) Now, let's look at the first given reaction (\( \mathrm{P}_{4}(s) + 6 \mathrm{Cl}_{2}(g) \longrightarrow 4 \mathrm{PCl}_{3}(g) \)). To get 6 PCl5 in our target reaction, we will need to reverse this first given reaction and multiply it by 1.5. This gives: \( 6 \mathrm{PCl}_{3}(g) \longrightarrow \mathrm{P}_{4}(s) + 9 \mathrm{Cl}_{2}(g) \, (-1.5\cdot \Delta H_1 = 1.5 \cdot 1225.6 \,\mathrm{kJ}) \) Next, let's work with the third given reaction (\( \mathrm{PCl}_{3}(g) + \mathrm{Cl}_{2}(g) \longrightarrow \mathrm{PCl}_{5}(g) \)). Since we reversed the first given reaction and obtained 6 PCl3 in it, we'll reverse this reaction also and multiply it by 6: \( 6 \mathrm{PCl}_{5}(g) \longrightarrow 6 \mathrm{PCl}_{3}(g) + 6 \mathrm{Cl}_{2}(g) \, (-6 \cdot \Delta H_3 = 6 \cdot 84.2 \, \mathrm{kJ}) \) Lastly, for the fourth given reaction (\( \mathrm{PCl}_{3}(g) + \frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{Cl}_{3} \mathrm{PO}(g) \)), we need 10 Cl3PO in our target reaction. So, we'll multiply it by 10: \( 10 \mathrm{PCl}_{3}(g) + 5 \mathrm{O}_{2}(g) \longrightarrow 10 \mathrm{Cl}_{3} \mathrm{PO}(g) \, (10 \cdot \Delta H_4 = 10 \cdot-285.7 \, \mathrm{kJ}) \)
03

3. Add the manipulated reactions

Now, let's add all the manipulated reactions together: \( 6 \mathrm{PCl}_{3}(g) \longrightarrow \mathrm{P}_{4}(s) + 9 \mathrm{Cl}_{2}(g) \, (1.5 \cdot 1225.6 \,\mathrm{kJ}) \) \( \mathrm{P}_{4}(s) + 5 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) \, (-2967.3 \,\mathrm{kJ}) \) \( 6 \mathrm{PCl}_{5}(g) \longrightarrow 6 \mathrm{PCl}_{3}(g) + 6 \mathrm{Cl}_{2}(g) \, (6 \cdot 84.2 \,\mathrm{kJ}) \) \( 10 \mathrm{PCl}_{3}(g) + 5 \mathrm{O}_{2}(g) \longrightarrow 10 \mathrm{Cl}_{3} \mathrm{PO}(g) \, (10 \cdot -285.7 \, \mathrm{kJ}) \) -------------------------------------------------------------------------------------------- \( \mathrm{P}_{4} \mathrm{O}_{10}(s) + 6 \mathrm{PCl}_{5}(g) \longrightarrow 10 \mathrm{Cl}_{3} \mathrm{PO}(g) \, (\Delta H_{target}) \)
04

4. Calculate the enthalpy change for the target reaction

Now, we can sum up the enthalpy changes from the manipulated reactions to find the enthalpy change for the target reaction: \( \Delta H_{target} = 1.5 \cdot 1225.6 - 2967.3 + 6 \cdot 84.2 + 10 \cdot (-285.7) \) \( \Delta H_{target} = 1838.4 - 2967.3 + 505.2 - 2857 \) \( \Delta H_{target} = -4470.7 \, \mathrm{kJ} \) The enthalpy change for the target reaction is -4470.7 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 91Ó°ÊÓ!

Key Concepts

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

Understanding Enthalpy Change
Enthalpy change is a fundamental concept in thermochemistry, representing the heat exchange at constant pressure during a chemical reaction. It is often denoted by \( \Delta H \), where a negative value indicates that the reaction releases heat (exothermic), while a positive value signifies that it absorbs heat (endothermic). This concept helps us understand how energy moves within chemical systems.

In our exercise, each given reaction comes with an enthalpy change value. These values help us determine the overall enthalpy change for the target reaction. Through Hess's Law, which states that enthalpy is a state function and thus the total enthalpy change depends only on the initial and final states, we can manipulate and combine these reactions. This allows us to calculate the enthalpy change for our target reaction using the given intermediary reactions.
The Role of Chemical Equations
Chemical equations are symbolic representations of chemical reactions, illustrating the reactants and products involved, along with their stoichiometric relationships. They are essential for applying Hess's Law to calculate enthalpy changes.

In our problem, each provided equation represents a segment of the larger reaction path needed to reach the target reaction. By analyzing these equations, we adjusted them to match the species and stoichiometry of our target reaction. For instance, we reversed and scaled some reactions to align them precisely with what the target reaction requires. This manipulation ensures that we can derive the correct overall enthalpy change by summing up the altered equations' enthalpy values.
Exploring Thermochemistry
Thermochemistry is the study of energy and heat associated with chemical reactions. It focuses on understanding the flow of energy through bonds and molecules and allows us to predict energy changes during reactions.

Utilizing concepts such as enthalpy and the representation of chemical reactions through equations, thermochemistry provides tools to quantify and compare the potential and energy changes within a system. With Hess's Law, we recognize that despite different pathways a reaction might take, the total enthalpy change remains consistent. This principle is vital for calculating the enthalpy of a complex reaction using simpler known reactions, as demonstrated in the problem where the aim was to find the enthalpy change for a multi-step reaction involving phosphorus compounds.

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 capacity of silver is 0.24 \(\mathrm{J} /^{\circ} \mathrm{C} \cdot \mathrm{g}\) a. Calculate the energy required to raise the temperature of 150.0 g Ag from 273 \(\mathrm{K}\) to 298 \(\mathrm{K}\) . b. Calculate the energy required to raise the temperature of 1.0 mole of \(\mathrm{Ag}\) by \(1.0^{\circ} \mathrm{C}\) (called the molar heat capacity of silver). c. It takes 1.25 \(\mathrm{kJ}\) of energy to heat a sample of pure silver from \(12.0^{\circ} \mathrm{C}\) to \(15.2^{\circ} \mathrm{C}\) . Calculate the mass of the sample of silver.

One of the components of polluted air is NO. It is formed in the high- temperature environment of internal combustion engines by the following reaction: $$ \mathrm{N}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}(g) \quad \Delta H=180 \mathrm{kJ} $$ Why are high temperatures needed to convert \(\mathrm{N}_{2}\) and \(\mathrm{O}_{2}\) to NO?

Using the following data, calculate the standard heat of formation of ICl \((g)\) in \(\mathrm{kJ} / \mathrm{mol} :\) $$\begin{array}{ll}{\mathrm{Cl}_{2}(g) \longrightarrow 2 \mathrm{Cl}(g)} & {\Delta H^{\circ}=242.3 \mathrm{kJ}} \\ {\mathrm{I}_{2}(g) \longrightarrow 2 \mathrm{I}(g)} & {\Delta H^{\circ}=151.0 \mathrm{kJ}} \\ {\mathrm{ICl}(g) \longrightarrow \mathrm{I}(g)+\mathrm{Cl}(g)} & {\Delta H^{\circ}=211.3 \mathrm{kJ}} \\ {\mathrm{I}_{2}(s) \longrightarrow \mathrm{I}_{2}(g)} & {\Delta H^{\circ}=62.8 \mathrm{kJ}}\end{array}$$

As a system increases in volume, it absorbs 52.5 \(\mathrm{J}\) of energy in the form of heat from the surroundings. The piston is working against a pressure of 0.500 \(\mathrm{atm} .\) The final volume of the system is 58.0 \(\mathrm{L}\) . What was the initial volume of the system if the internal energy of the system decreased by 102.5 \(\mathrm{J} ?\)

In a coffee-cup calorimeter, 1.60 \(\mathrm{g} \mathrm{NH}_{4} \mathrm{NO}_{3}\) is mixed with 75.0 \(\mathrm{g}\) water at an initial temperature of \(25.00^{\circ} \mathrm{C}\) . After dissolution of the salt, the final temperature of the calorimeter contents is \(23.34^{\circ} \mathrm{C}\) . Assuming the solution has a heat capacity of 4.18 \(\mathrm{J} / \mathrm{C} \cdot \mathrm{g}\) and assuming no heat loss to the calorimeter, calculate the enthalpy change for the dissolution of \(\mathrm{NH}_{4} \mathrm{NO}_{3}\) in units of kJ/mol.

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.