Problem 116
Question
Calculate \(\mathrm{Q}\) and \(\mathrm{W}\) for the isothermal reversible expansion of one mole of an ideal gas from an initial pressure of \(1.0\) bar to a final pressure of \(0.1\) bar at a constant temperature of \(273 \mathrm{~K}\). (a) \(5.22 \mathrm{~kJ},-5.22 \mathrm{~kJ}\) (b) \(-27.3 \mathrm{~kJ}, 27.3 \mathrm{~kJ}\) (c) \(27.3 \mathrm{~kJ},-27.3 \mathrm{~kJ}\) (d) \(-5.22 \mathrm{~kJ}, 5.22 \mathrm{~kJ}\)
Step-by-Step Solution
Verified Answer
(d) -5.22 kJ, 5.22 kJ
1Step 1: Understand the process
The problem involves isothermal reversible expansion of one mole of an ideal gas. The temperature remains constant at 273 K throughout this process.
2Step 2: Apply the Ideal Gas Law
Since it is an isothermal process, we use the ideal gas equation in the form: \[ P_1 V_1 = P_2 V_2 \] Where \( P_1 = 1.0 \text{ bar} \), \( P_2 = 0.1 \text{ bar} \). This allows us to express the volumes in terms of pressures assuming constant temperature.
3Step 3: Calculate the Work Done
For an isothermal reversible process, the work done \( W \) on or by the gas can be described by:\[ W = nRT \ln \frac{V_2}{V_1} \]Substitute \( V_1 \) and \( V_2 \) in terms of pressure:\[ W = nRT \ln \frac{P_1}{P_2} \]where \( n = 1 \), \( R = 8.314 \text{ J/mol·K} \), and \( T = 273 \text{ K} \).Calculate the work:\[ W = (1)(8.314)(273) \ln \frac{1.0}{0.1} \]\[ W = 2270.622 \ln 10 \approx 2270.622 \times 2.302 \approx 5230 \text{ J} \approx 5.23 \text{ kJ} \]
4Step 4: Determine the Relationship Between Q and W
In an isothermal process, the internal energy change \( \Delta U \) is zero for an ideal gas. Thus, the heat absorbed \( Q \) is equal to the work done \( W \):\[ Q = -W \]Therefore, \( Q = -5.23 \text{ kJ} \) when \( W = 5.23 \text{ kJ} \).
5Step 5: Match to Answer Choices
The calculated values are \( Q = -5.23 \text{ kJ} \) and \( W = 5.23 \text{ kJ} \). Compare this with the given options. The closest match is option (d): \(-5.22 \text{ kJ}, 5.22 \text{ kJ}\).
Key Concepts
Ideal Gas LawWork DoneTemperatureHeat Absorbed
Ideal Gas Law
The ideal gas law is a fundamental principle in chemistry and physics used to relate the pressure, volume, and temperature of an ideal gas. In this exercise, the situation is the isothermal expansion of an ideal gas, meaning the temperature remains constant. The formula that embodies the ideal gas law is:
- \[ PV = nRT \]
- \(P\) is the pressure of the gas,
- \(V\) is the volume,
- \(n\) is the number of moles,
- \(R\) is the universal gas constant (8.314 J/mol·K), and
- \(T\) is the temperature in Kelvin.
Work Done
In thermodynamics, the concept of work done is vital to understanding how energy is transferred during processes. When dealing with gas in a cylinder with a movable piston, work is done by the gas on the surroundings when it expands. Specifically for isothermal reversible processes involving ideal gases, the work done \( W \) can be calculated by the integral of pressure with respect to volume. Ultimately, this can be simplified to:
- \[ W = nRT \ln \frac{V_2}{V_1} \]
- \[ W = nRT \ln \frac{P_1}{P_2} \]
Temperature
Temperature plays a crucial role in gas behavior and thermodynamic processes. In this specific exercise, the process described is isothermal, meaning the temperature remains constant throughout. The significance of constant temperature in an isothermal process is that it simplifies calculations and makes energy exchange straightforward, particularly for ideal gases. For an ideal gas at constant temperature:
- The internal energy \( \Delta U \) of the system remains unchanged.
- An increase in volume leads to a corresponding decrease in pressure, without altering the internal energy.
Heat Absorbed
Heat absorbed by a gas during expansion is a critical part of thermodynamic studies. In the case of an isothermal process for an ideal gas, the internal energy change \( \Delta U \) is zero, because internal energy depends only on temperature, which is constant. This leads to a straightforward relationship between heat \( Q \) and work \( W \).
- The first law of thermodynamics states that: \[ \Delta U = Q - W \]
- For isothermal processes, since \( \Delta U = 0 \), it implies that:\[ Q = W \]
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