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Determine the free energy change, \(\Delta \mathrm{G}\), for transforming liquid water at \(100^{\circ} \mathrm{C}\) and 1 atm. to vapor at the same conditions. \(\Delta \mathrm{H}=9720\) cal (molar enthalpy of vaporization).

Short Answer

Expert verified
The free energy change, \(\Delta G\), for transforming liquid water at \(100^{\circ} \mathrm{C}\) and 1 atm to vapor at the same conditions is \(\Delta G = 9720 \,\text{cal}\).

Step by step solution

01

Convert given temperature to Kelvin

The given temperature is in Celsius, we need to convert it to Kelvin for our calculations. The conversion formula is: Temperature in Kelvin (K) = Temperature in Celsius (°C) + 273.15 So, temperature in Kelvin is: \(T = 100 + 273.15 = 373.15 K\)
02

Use the enthalpy change and Clausius-Clapeyron equation to find the entropy change

The Clausius-Clapeyron equation is given as: \[\ln\left(\frac{P_{2}}{P_{1}}\right) = \frac{-\Delta H}{R} \left(\frac{1}{T_2} - \frac{1}{T_1}\right)\] Since the pressure is the same for both states (1 atm), we have \(P_1 = P_2\), which means the left side of the equation becomes 0. Therefore, we have: \(0 = \frac{-\Delta H}{R} \left(\frac{1}{T_2} - \frac{1}{T_1}\right)\) Since the equation equals to 0, we can discard \(\Delta H\) and \(R\). Thus, we are left with the following: \(0 = \frac{1}{T_2} - \frac{1}{T_1}\) By the statement "at the same conditions," we also have \(T_1 = T_2\). Therefore, the entropy change, \(\Delta S\), for this process is 0.
03

Calculate the free energy change

Now that we have found the entropy change, we can use the relationship between free energy change, enthalpy change, and entropy change to find the free energy change \(\Delta \mathrm{G}\). This relationship is given as: \(\Delta \mathrm{G} = \Delta \mathrm{H} - T\Delta \mathrm{S}\) Since we found that \(\Delta \mathrm{S} = 0\), the formula simplifies to: \(\Delta \mathrm{G} = \Delta \mathrm{H}\) Using the given enthalpy change, we can find the free energy change: \(\Delta \mathrm{G} = 9720 \,\text{cal}\)
04

Present the final result

The free energy change for transforming liquid water at \(100^{\circ} \mathrm{C}\) and 1 atm to vapor at the same conditions is: \(\Delta \mathrm{G} = 9720 \,\text{cal}\)

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Key Concepts

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

Clausius-Clapeyron Equation
The Clausius-Clapeyron equation is a fundamental principle in thermodynamics that describes the relationship between the pressure and temperature of two phases of a substance in equilibrium, such as the liquid and vapor states of water. With this equation, students can calculate how the vapor pressure of a substance changes with temperature—a crucial aspect for understanding phase transitions.

This equation is particularly useful for predicting how much pressure is required to boil or condense a substance at a specific temperature. In simple terms, it tells us how temperature and vapor pressure are related for a pure substance during phase changes. The equation is expressed as:
\[\ln\left(\frac{P_{2}}{P_{1}}\right) = \frac{-\Delta H}{R} \left(\frac{1}{T_2} - \frac{1}{T_1}\right)\]
where:
  • \(P_1\) and \(P_2\) are the pressures at temperatures \(T_1\) and \(T_2\), respectively
  • \(\Delta H\) represents the enthalpy change of the phase transition
  • \(R\) is the universal gas constant
Understanding this equation aids in comprehension of how energy is absorbed or released during a phase change.
Enthalpy of Vaporization
The enthalpy of vaporization, symbolized as \(\Delta H_{vap}\), is the amount of energy required to convert a given quantity of a substance from a liquid into a vapor without changing its temperature. This thermodynamic quantity is a measure of the energy barrier that molecules need to overcome to escape from the liquid phase and enter the gas phase.

The enthalpy of vaporization is a crucial concept in calculations involving phase changes, especially when substances transition from liquid to gas, such as the boiling of water. This energy is absorbed from the surroundings, and thus it is considered endothermic. The enthalpy of vaporization can be experimentally determined and is often provided in calories per mole or joules per mole. For instance, the exercise provided an enthalpy of vaporization of \(9720 \text{cal}\) for water to vaporize.
Gibbs Free Energy
Gibbs free energy, or \(\Delta G\), is an essential concept in thermodynamics that represents the maximum amount of work that can be performed by a thermodynamic process at constant temperature and pressure. It is a state function that helps predict the direction of chemical reactions and phase transitions.

It is calculated using the formula:\[\Delta G = \Delta H - T\Delta S\]
where:
  • \(\Delta H\) is the change in enthalpy
  • \(T\) is the temperature in Kelvin
  • \(\Delta S\) is the change in entropy
In a process where the temperature and pressure are constant, if \(\Delta G\) is negative, the process occurs spontaneously. On the other hand, if \(\Delta G\) is positive, the process is nonspontaneous and requires input of energy to occur. Understanding the relationship between Gibbs free energy, enthalpy, and entropy allows us to predict the feasibility of a reaction or process under given conditions.
Thermodynamics
Thermodynamics is the branch of physical science that deals with the relations between heat and other forms of energy. It describes how energy is transferred within systems and how it affects matter, allowing us to understand phenomena such as heat engines, refrigerators, and reactions in living organisms.

One of the key themes in thermodynamics is the law of conservation of energy, which states that energy cannot be created or destroyed, only transformed from one form into another. There are four main laws of thermodynamics that define physical quantities, such as temperature, energy, and entropy, and illustrate how they are interrelated and how they can predict the behavior of a given system.
In summary, thermodynamics helps us understand the energy changes that accompany physical and chemical processes, providing the theoretical underpinning for many practical applications in engineering, chemistry, biology, and environmental science.

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Most popular questions from this chapter

Sulfur exists as \(S_{2}\) vapor at temperatures between \(700^{\circ} \mathrm{C}\) and \(1500^{\circ} \mathrm{C}\). At \(1473 \mathrm{k}\) it combines with hydrogen according to the equation $$ \mathrm{H}_{2}(\mathrm{~g})+(1 / 2) \mathrm{S}_{2}(\mathrm{~g}) \rightarrow \mathrm{H}_{2} \mathrm{~S}(\mathrm{~g}) $$ At \(750^{\circ} \mathrm{C}\) the equilibrium constant is \(1.07 \times 10^{2}\) and at \(1200^{\circ} \mathrm{C}\) it is \(4.39\). Determine the heat of reaction in the temperature range \(750^{\circ} \mathrm{C}\) to \(1200^{\circ} \mathrm{C}\), and the change in free energy at each of these temperatures.

The equilibrium constant and standard Gibbs free energy change for ammonia synthesis at \(400^{\circ} \mathrm{C}\) or \(673^{\circ} \mathrm{K}\) are \(1.64 \times\) \(10^{-4}\) and \(11,657 \mathrm{cal} /\) mole, respectively. The equation for this reaction is (1) \(\quad \mathrm{N}_{2}(\mathrm{~g})+3 \mathrm{H}_{2}(\mathrm{~g}) \rightarrow 2 \mathrm{NH}_{3}(\mathrm{~g})\) Calculate the equilibrium constants and standard free energy changes for (2) \((1 / 2) \mathrm{N}_{2}(\mathrm{~g})+3 / 2 \mathrm{H}_{2}(\mathrm{~g})=\mathrm{NH}_{3}(\mathrm{~g})\) and (3) \(2 \mathrm{NH}_{3}(\mathrm{~g}) \rightarrow \mathrm{N}_{2}(\mathrm{~g})+3 \mathrm{H}_{2}(\mathrm{~g})\)

Calculate the equilibrium constant at \(25^{\circ} \mathrm{C}\) for the reaction: $$ \mathrm{S}+3 / 2 \mathrm{O}_{2} \rightleftarrows \mathrm{SO}_{3} $$ The heat formation of \(\mathrm{SO}_{3}\) at \(25^{\circ} \mathrm{C}\) is \(-94.45 \mathrm{Kcal} / \mathrm{mole}\) and the standard molar entropy changes for \(\mathrm{S}, \mathrm{O}_{2}\), and \(\mathrm{SO}_{3}\) at \(25^{\circ} \mathrm{C}\) are \(7.62,49.0\) and \(61.24 \mathrm{cal} / \mathrm{mole}^{\circ} \mathrm{K}\), respectively.

Calculate \(\Delta \mathrm{S}\) for the conversion of one mole of liquid water to vapor at \(100^{\circ} \mathrm{C}\). Heat of vaporization \(=540 \mathrm{cal} / \mathrm{g}\).

Given, for acetic acid that \(\Delta \mathrm{H}_{\text {fus }}=2592\) cal/mole at its melting point, \(16.6^{\circ} \mathrm{C}\) and \(\Delta \mathrm{H}_{\mathrm{VAP}}=5808 \mathrm{cal} / \mathrm{mole}\) at its boiling point, \(118.3^{\circ} \mathrm{C}\), calculate the change in entropy that takes place when 1 mole of the vapor is condensed at its boiling point and changed to a solid at its melting point, all under constant pressure, taken as 1 atm. Assume that the molar heat capacity of acetic acid is \(27.6 \mathrm{cal} /\) deg \(-\) mole.

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