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Determine the change in the Gibbs function for \(\mathrm{H}_{2}+\) \(\frac{1}{2} \mathrm{O}_{2} \rightarrow \mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) in \(\mathrm{kJ}\) per kmol of \(\mathrm{H}_{2}(\mathrm{~g})\) using enthalpy of formation data at \(25^{\circ} \mathrm{C}\) and \(1 \mathrm{~atm}\).

Short Answer

Expert verified
-228.5 kJ per kmol H\textsubscript{2}(g)

Step by step solution

01

Write the Chemical Reaction

Identify the given balanced chemical equation: \[ \mathrm{H}_{2} + \frac{1}{2} \mathrm{O}_{2} \rightarrow \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \]
02

Gather Enthalpy of Formation Data

Look up the standard enthalpy of formation values at 25°C (298 K) and 1 atm: \[ \Delta H_f^0 (\mathrm{H}_2(\mathrm{g})) = 0 \ \Delta H_f^0 (\mathrm{O}_2(\mathrm{g})) = 0 \ \Delta H_f^0 (\mathrm{H}_2\mathrm{O}(\mathrm{g})) = -241.8 \, \text{kJ/mol} \]
03

Calculate the Enthalpy Change of the Reaction

Use the enthalpy of formation data to calculate the enthalpy change, \(\Delta H\), of the reaction: \[ \Delta H = \sum_{\text{products}} n \Delta H_f^0 - \sum_{\text{reactants}} n \Delta H_f^0 \ \Delta H = [1 \times (-241.8)] - [1 \times 0 + \frac{1}{2} \times 0] = -241.8 \, \text{kJ/mol} \]
04

Gather Entropy Data

Look up the standard entropy values at 25°C (298 K) and 1 atm: \[ S^0(\mathrm{H}_2(\mathrm{g})) = 130.68 \, \text{J/(mol·K)} \ S^0(\mathrm{O}_2(\mathrm{g})) = 205.0 \, \text{J/(mol·K)} \ S^0(\mathrm{H}_2\mathrm{O}(\mathrm{g})) = 188.83 \, \text{J/(mol·K)} \]
05

Calculate the Entropy Change of the Reaction

Use the provided entropy values to calculate the entropy change, \(\Delta S\), of the reaction: \[ \Delta S = \sum_{\text{products}} n S^0 - \sum_{\text{reactants}} n S^0 \ \Delta S = [1 \times 188.83] - [1 \times 130.68 + \frac{1}{2} \times 205.0] = -44.6 \, \text{J/(mol·K)} = -0.0446 \, \text{kJ/(mol·K)} \]
06

Apply the Gibbs Free Energy Equation

Apply the Gibbs Free Energy equation to find \(\Delta G\): \[ \Delta G = \Delta H - T \Delta S \ \Delta G = -241.8 \, \text{kJ/mol} - (298 \, \text{K}) \times (-0.0446 \, \text{kJ/(mol·K)}) \ \Delta G = -241.8 + 13.3 = -228.5 \, \text{kJ/mol} \]

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Key Concepts

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

Enthalpy of Formation
Enthalpy of formation, often denoted as \( \Delta H_f^0 \), refers to the heat change that occurs when one mole of a compound is formed from its elements in their standard states. This is usually measured under standard conditions of 25°C (298 K) and 1 atmosphere pressure.
In our exercise, we want to determine the Gibbs free energy change for a reaction involving hydrogen and oxygen. We start by identifying the enthalpy of formation values for the substances in the reaction:
  • \( \mathrm{H}_2(\mathrm{g}) \) and \( \mathrm{O}_2(\mathrm{g}) \) have \( \Delta H_f^0 \) values of 0 because they are in their standard states.
  • \( \mathrm{H}_2\textrm{O}(\mathrm{g}) \) has an enthalpy of formation value of -241.8 kJ/mol.

Using these values, we can calculate the enthalpy change (\( \Delta H \)) for the reaction according to:
\( \Delta H = \sum_{\text{products}} n \Delta H_f^0 - \sum_{\text{reactants}} n \Delta H_f^0 \)
Substituting the respective values and coefficients in the balanced equation, we get:
  • \[ \Delta H = [1 \times (-241.8)] - [1 \times 0 + \frac{1}{2} \times 0]\br= -241.8 \textrm{kJ/mol} \]
Entropy Change
Another key concept in our problem is entropy change, represented by \( \Delta S \). Entropy is a measure of the randomness or disorder of a system. Each substance has a standard molar entropy, denoted by \( S^0 \).
For the reaction, we use the following standard entropy values at 25°C (298 K) and 1 atm:
  • \( \mathrm{H}_2(\textrm{g}) \): 130.68 J/(mol·K)
  • \( \mathrm{O}_2(\textrm{g}) \): 205.0 J/(mol·K)
  • \( \mathrm{H}_2\textrm{O}(\textrm{g}) \): 188.83 J/(mol·K)

Using these values, we calculate the entropy change of the reaction:
\[ \Delta S = \sum_{\textrm{products}} n S^0 - \sum_{\textrm{reactants}} n S^0 \]
Substituting the values and coefficients, we obtain:
  • \[ \Delta S = [1 \times 188.83] - [1 \times 130.68 + \frac{1}{2} \times 205.0]\br= -44.6 \textrm{J/(mol·K)} = -0.0446 \textrm{kJ/(mol·K)} \]
Chemical Reaction
A chemical reaction occurs when substances, known as reactants, transform into different substances called products. This transformation involves breaking old bonds and forming new ones.
In our exercise, the balanced chemical equation is:
\[ \mathrm{H}_{2} + \frac{1}{2} \mathrm{O}_{2} \rightarrow \mathrm{H}_{2} \mathrm{O} (\mathrm{g}) \]
Here, hydrogen gas (\textrm{H}_2) and oxygen gas (\textrm{O}_2) react to form water vapor (\textrm{H}_2\textrm{O}).
The change in Gibbs free energy (\( \Delta G \)) helps understand the spontaneity of the reaction. We calculate it using Gibbs free energy equation:
  • \[ \Delta G = \Delta H - T \Delta S \]
Substituting our calculated values for \( \Delta H \) and \( \Delta S \), and considering T = 298 K:
  • \[ \Delta G = -241.8 \textrm{kJ/mol} - (298 \textrm{K}) \times (-0.0446 \textrm{kJ/(mol·K)})\br= -241.8 + 13.3\br= -228.5 \textrm{kJ/mol} \]
This indicates that the reaction is spontaneous under standard conditions.

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Most popular questions from this chapter

An inventor has developed a device that at steady state takes in liquid water at \(25^{\circ} \mathrm{C}, 1 \mathrm{~atm}\) with a mass flow rate of \(4 \mathrm{~kg} / \mathrm{h}\) and produces separate streams of hydrogen \(\left(\mathrm{H}_{2}\right.\) ) and oxygen \(\left(\mathrm{O}_{2}\right)\), each at \(25^{\circ} \mathrm{C}, 1 \mathrm{~atm}\). The inventor claims that the device requires an electrical power input of \(14.6 \mathrm{~kW}\) when operating isothermally at \(25^{\circ} \mathrm{C}\). Heat transfer with the surroundings occurs, but kinetic and potential energy effects can be ignored. Evaluate the inventor's claim.

Butane \(\left(\mathrm{C}_{4} \mathrm{H}_{10}\right)\) at \(25^{\circ} \mathrm{C}, 1 \mathrm{~atm}\) enters a combustion chamber operating at steady state and burns completely with the theoretical amount of air entering at the same conditions. If the products exit at \(93^{\circ} \mathrm{C}, 1 \mathrm{~atm}\), determine the rate of heat transfer from the combustion chamber, in \(\mathrm{kJ}\) per \(\mathrm{kmol}\) of fuel. Kinetic and potential energy effects are negligible.

Octane gas \(\mathrm{C}_{8} \mathrm{H}_{18}\) at \(25^{\circ} \mathrm{C}\) enters a jet engine and burns completely with \(300 \%\) of theoretical air entering at \(25^{\circ} \mathrm{C}\), \(1 \mathrm{~atm}\) with a volumetric flow rate of \(42 \mathrm{~m}^{3} / \mathrm{s}\). Products of combustion exit at \(990 \mathrm{~K}, 1 \mathrm{~atm}\). If the fuel and air enter with negligible velocities, determine the thrust produced by the engine in \(\mathrm{kN}\).

When I burn wood in my fireplace, do I contribute to global warming? Explain.

Butane \(\left(\mathrm{C}_{4} \mathrm{H}_{10}\right)\) burns completely with air. The equivalence ratio is \(0.85\). Determine (a) the balanced reaction equation. (b) the percent excess air.

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