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

The enthalpy of combustion of \(\mathrm{CH}_{4}(g)\) when \(\mathrm{H}_{2} \mathrm{O}(l)\) is formed is \(-891 \mathrm{kJ} / \mathrm{mol}\) and the enthalpy of combustion of \(\mathrm{CH}_{4}(g)\) when \(\mathrm{H}_{2} \mathrm{O}(g)\) is formed is \(-803 \mathrm{kJ} / \mathrm{mol} .\) Use these data and Hess's law to determine the enthalpy of vaporization for water.

Short Answer

Expert verified
The enthalpy of vaporization for water (ΔHvap) can be determined using Hess's Law and the given enthalpy of combustion values for CH4(g). By subtracting the first reaction (when H2O(l) is formed) from the second reaction (when H2O(g) is formed), we obtain the reaction 2H2O(l) -> 2H2O(g) with an enthalpy change of ΔHvap = ΔH2 - ΔH1. Substituting the given values, we find that ΔHvap = (-803 kJ/mol) - (-891 kJ/mol), which gives us an enthalpy of vaporization for water of 88 kJ/mol.

Step by step solution

01

Write down the given reactions

First, let's write down the given reactions and their enthalpies: 1. CH4(g) + 2O2(g) -> CO2(g) + 2H2O(l) ΔH1 = -891 kJ/mol 2. CH4(g) + 2O2(g) -> CO2(g) + 2H2O(g) ΔH2 = -803 kJ/mol And we need to determine the enthalpy of vaporization for water (ΔHvap).
02

Understand Hess's Law

Hess's Law states that the total enthalpy change for a chemical reaction is the same, no matter whether it happens in one step or multiple steps. So, if we can create a reaction that represents the enthalpy of vaporization for water using the given reactions, then we can find the ΔHvap for water.
03

Create a new reaction representing the enthalpy of vaporization

We can achieve this by subtracting the first reaction from the second reaction. This will give us a new reaction representing the vaporization of H2O: Reaction 3: 2H2O(l) -> 2H2O(g) ΔH3 = ΔHvap = ΔH2 - ΔH1 Now we just need to calculate ΔHvap by substituting the values of ΔH1 and ΔH2.
04

Calculate ΔHvap for water

ΔHvap = ΔH2 - ΔH1 ΔHvap = (-803 kJ/mol) - (-891 kJ/mol)
05

Solve for ΔHvap

ΔHvap = 88 kJ/mol So, the enthalpy of vaporization for water is 88 kJ/mol.

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 of Combustion
The enthalpy of combustion is one of the key concepts in chemical thermodynamics. It refers to the heat released when one mole of a substance reacts completely with oxygen under standard conditions. Combustion reactions are typically exothermic, meaning they release energy in the form of heat.

In the context of the exercise, we look at the enthalpy of combustion for methane (\(\mathrm{CH}_4\)), which is a commonly used fuel. We have two enthalpy values:
  • \(-891 \mathrm{kJ/mol}\) when \(\mathrm{H}_2\mathrm{O}(l)\) is formed.
  • \(-803 \mathrm{kJ/mol}\) when \(\mathrm{H}_2\mathrm{O}(g)\) is formed.
These values indicate the energy difference between liquid and gaseous water as they form. It's crucial to understand these differences because they relate to the physical state of water during the reactions, directly influencing the total heat exchanged.
Enthalpy of Vaporization
The enthalpy of vaporization (\(\Delta H_{vap}\)) is a term used to define the amount of energy needed to convert a liquid into a gas. It is a fundamental concept when discussing phase changes at a constant temperature.

In our problem, we are calculating the vaporization enthalpy for water (\(\mathrm{H}_2\mathrm{O}\)), demonstrating how to use Hess's Law in solving this. According to Hess's Law, the enthalpy change of this phase transition is based on the subtraction of two given reaction enthalpies:
  • Combustion leading to liquid water: \(-891 \mathrm{kJ/mol}\).
  • Combustion leading to gaseous water: \(-803 \mathrm{kJ/mol}\).
The difference \(88 \mathrm{kJ/mol}\) represents the enthalpy required to convert water from its liquid form into vapor under the same conditions. This makes it an important value in understanding energy changes during boiling or evaporation.
Chemical Thermodynamics
Chemical thermodynamics is the study of energy transformations in chemical processes. This discipline helps us understand how energy is absorbed or released during reactions, and it's key for predicting reaction behavior and designing chemical processes.

In terms of our exercise, the principle of Hess's Law illustrates how chemical thermodynamics can be used to calculate unknown energy changes. Hess's Law states that the total enthalpy change for a reaction is the same, irrespective of the pathway by which the reaction takes place. This is incredibly useful for calculating values like the enthalpy of vaporization, as demonstrated.

Understanding chemical thermodynamics allows scientists and engineers to harness and optimize energy usage in industrial applications. It provides the framework for processes such as combustion, phase changes like vaporization, and countless other applications that depend on controlled energy transformations.

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

Consider a mixture of air and gasoline vapor in a cylinder with a piston. The original volume is \(40 . \mathrm{cm}^{3} .\) If the combustion of this mixture releases \(950 .\) \(\mathrm{J}\) of energy, to what volume will the gases expand against a constant pressure of \(650 .\) torr if all the energy of combustion is converted into work to push back the piston?

A sample of nickel is heated to \(99.8^{\circ} \mathrm{C}\) and placed in a coffeecup calorimeter containing \(150.0 \mathrm{g}\) water at \(23.5^{\circ} \mathrm{C}\). After the metal cools, the final temperature of metal and water mixture is \(25.0^{\circ} \mathrm{C} .\) If the specific heat capacity of nickel is \(0.444 \mathrm{J} /^{\circ} \mathrm{C} \cdot \mathrm{g}\) what mass of nickel was originally heated? Assume no heat loss to the surroundings.

The bomb calorimeter in Exercise 102 is filled with 987 g water. The initial temperature of the calorimeter contents is \(23.32^{\circ} \mathrm{C} . \mathrm{A}\) \(1.056-\mathrm{g}\) sample of benzoic acid \(\left(\Delta E_{\text {comb }}=-26.42 \mathrm{kJ} / \mathrm{g}\right)\) is combusted in the calorimeter. What is the final temperature of the calorimeter contents?

How is average bond strength related to relative potential energies of the reactants and the products?

A piston performs work of \(210 . \mathrm{L}\). \(\mathrm{atm}\) on the surroundings, while the cylinder in which it is placed expands from \(10. \mathrm{L}\) to \(25 \mathrm{L}\). At the same time, \(45 \mathrm{J}\) of heat is transferred from the surroundings to the system. Against what pressure was the piston working?

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