For a reversible process at \(T=300 \mathrm{~K}\), volume of the ideal gas is increased from \(1 \mathrm{~L}\) to \(10 \mathrm{~L}\). If the process is isothermal, the \(\Delta H\) of the process is (a) \(11.47 \mathrm{~kJ}\) (b) \(4.98 \mathrm{~kJ}\) (c) 0 (d) \(-11.47 \mathrm{~kJ}\)

Short Answer

Expert verified
The change in enthalpy (\rewline(\(\Delta H\))) for an ideal gas in an isothermal process at constant temperature is 0 (option (c)).

Step by step solution

01

Understanding the properties of an ideal gas process

For an ideal gas undergoing an isothermal process (constant temperature), the change in enthalpy (\rewline(\(\Delta H\))) is a function of the change in pressure and volume. However, because internal energy (\rewline(\(U\))) is only a function of temperature for an ideal gas, and enthalpy (\rewline(\(H\))) is defined as (\rewline(\(H = U + PV\))), at constant temperature and for an ideal gas, the change in enthalpy is zero, as the change in internal energy is zero.
02

Applying the first law of thermodynamics

According to the first law of thermodynamics, which states that (\rewline(\(\Delta U = Q - W\))), where (\rewline(\(\Delta U\))) is the change in internal energy, (\rewline(\(Q\))) is the heat added to the system, and (\rewline(\(W\))) is work done by the system. For an isothermal process of an ideal gas, (\rewline(\(\Delta U\))) is zero, hence (\rewline(\(Q = W\))). Consequently, any heat added to the system is equal to the work done by the gas, but this does not affect the enthalpy change, which remains zero at constant temperature.
03

Analyzing the options

Given the information above, that (\rewline(\(\Delta H\))) for an isothermal process in an ideal gas is zero at constant temperature, we can determine that the correct answer does not depend on calculating any work or heat exchange, but rather understanding the thermodynamic properties of ideal gases.

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Key Concepts

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

Ideal Gas Law
When learning about thermodynamics, an essential concept is the Ideal Gas Law, which is defined by the equation \(PV = nRT\), where \(P\) represents pressure, \(V\) volume, \(n\) moles of gas, \(R\) the ideal gas constant, and \(T\) temperature. This law correlates the pressure, volume, temperature, and amount of an ideal gas within a system in a simple way.

An isothermal process, such as the one described in our exercise, assumes that the temperature (\(T\)) remains constant. Under this condition, the Ideal Gas Law implies that pressure and volume are inversely related; as one increases, the other must decrease. Thus, if you increase the volume of an ideal gas at constant temperature, the pressure must decrease to maintain the equality \(PV = nRT\). However, when dealing with enthalpy changes in isothermal processes, this information alone is not enough, as we also need to consider the first law of thermodynamics and properties of internal energy.
First Law of Thermodynamics
The First Law of Thermodynamics is a statement of energy conservation, which in the context of thermodynamics means that the total internal energy of an isolated system is constant unless acted upon by external work or heat transfer. Expressed mathematically, it is \(\Delta U = Q - W\), where \(\Delta U\) is the change in internal energy, \(Q\) is the heat added to the system, and \(W\) is the work done by the system.

For an isothermal process involving an ideal gas, where temperature is constant, we can infer that internal energy remains unchanged (\(\Delta U = 0\)) because the internal energy of an ideal gas is a function of temperature. Since any heat added to the system (\(Q\)) will be equal to the work done by the system (\(W\)), the internal energy does not change. Importantly, this means that even when work is done or heat is transferred, this does not result in a change in the internal energy or enthalpy in an isothermal process for an ideal gas.
Internal Energy of Ideal Gas
The concept of Internal Energy of an Ideal Gas is tied closely to its temperature. Internal energy (\(U\)) is the total energy contained by a system's particles, mainly due to kinetic energy because ideal gas particles are assumed not to interact with each other except during elastic collisions.

In our exercise, since the temperature remains constant in an isothermal process, and because internal energy for an ideal gas is only temperature-dependent, no change in internal energy occurs. This fact allows us to simplify the first law of thermodynamics to the relationship \(Q = W\) in the context of the given process. It is important for students to understand that in this scenario, despite the volume change, the lack of temperature change means that the internal energy stays the same, as does the enthalpy.
Enthalpy of Ideal Gas
The Enthalpy of an Ideal Gas, represented as \(H\), is another state function, which includes the internal energy plus the product of the pressure and the volume of the gas (\(H = U + PV\)). Because enthalpy is also a function of temperature for an ideal gas, during an isothermal process where the temperature does not vary, neither does the enthalpy.

In the context of the question we reviewed, since the process is isothermal and the gas is ideal, the change in enthalpy (\(\Delta H\)) is effectively zero. It might be confusing when considering that volume changes, as one might think this would affect the \(PV\) term in the enthalpy formula. However, the pressure adjusts inversely to volume due to the Ideal Gas Law, keeping the product \(PV\) constant and thereby keeping the enthalpy (\(H\)) constant as well. This understanding is crucial when sorting through potential answers to homework problems that involve thermodynamics and physical chemistry.

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Most popular questions from this chapter

Which of the following would be expected to have the largest entropy per mole? (a) \(\mathrm{SO}_{2} \mathrm{Cl}_{2}(\mathrm{~s})\) (b) \(\mathrm{SO}_{2} \mathrm{Cl}_{2}(\mathrm{I})\) (c) \(\mathrm{SO}_{2} \mathrm{Cl}_{2}(\mathrm{~g})\) (d) \(\mathrm{SO}_{2}(\mathrm{~g})\)

The values of \(\Delta G\) are very important in metallurgy. The \(\Delta G\) values for the following reactions at \(1000 \mathrm{~K}\) are given as: \(\mathrm{S}_{2}(\mathrm{~s})+2 \mathrm{O}_{2}(\mathrm{~g}) \rightarrow 2 \mathrm{SO}_{2}(\mathrm{~g}) ; \Delta G=-544 \mathrm{~kJ}\) \(2 \mathrm{Zn}(\mathrm{s})+\mathrm{S}_{2}(\mathrm{~s}) \rightarrow 2 \mathrm{ZnS}(\mathrm{s}) ; \Delta G=-293 \mathrm{~kJ}\) \(2 \mathrm{Zn}(\mathrm{s})+\mathrm{O}_{2}(\mathrm{~g}) \rightarrow 2 \mathrm{ZnO}(\mathrm{s}) ; \Delta G=-480 \mathrm{~kJ}\) The \(\Delta G\) for the reaction: \(2 \mathrm{ZnS}(\mathrm{s})+3 \mathrm{O}_{2}(\mathrm{~g}) \rightarrow 2 \mathrm{ZnO}(\mathrm{s})+2 \mathrm{SO}_{2}(\mathrm{~g})\) will be (a) \(-357 \mathrm{~kJ}\) (b) \(-731 \mathrm{~kJ}\) (c) \(-773 \mathrm{~kJ}\) (d) \(-229 \mathrm{~kJ}\)

The entropy change in the fusion of one mole of a solid melting at \(300 \mathrm{~K}\) (latent heat of fusion, \(2930 \mathrm{~J} / \mathrm{mol}\) ) is (a) \(9.77 \mathrm{~J} / \mathrm{K}-\mathrm{mol}\) (b) \(10.73 \mathrm{~J} / \mathrm{K}-\mathrm{mol}\) (c) \(2930 \mathrm{~J} / \mathrm{K}-\mathrm{mol}\) (d) \(108.5 \mathrm{~J} / \mathrm{K}-\mathrm{mol}\)

For a system in equilibrium, \(\Delta G=0\) under conditions of constant (a) temperature and pressure (b) temperature and volume (c) pressure and volume (d) energy and volume

An adiabatic cylinder fitted with an adiabatic piston at the right end of cylinder, is divided into two equal halves with a monoatomic gas on left side and diatomic gas on right side, using an impermeable movable adiabatic wall. If the piston is pushed slowly to compress the diatomic gas to \(\frac{3}{4}\) th of its original volume. The ratio of new volume of monoatomic gas to its initial volume would be (a) \(\left(\frac{4}{3}\right)^{\frac{25}{21}}\) (b) \(\left(\frac{7}{5}\right)^{\frac{3}{4}}\) (c) \(\left(\frac{3}{4}\right)^{\frac{21}{25}}\) (d) \(\frac{3}{4}\)

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