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The volume of \(0.100 \mathrm{~mol}\) of helium gas at \(27^{\circ} \mathrm{C}\) is increased isothermally from \(2.00 \mathrm{~L}\) to \(5.00 \mathrm{~L}\). Assuming the gas to be ideal, calculate the entropy change for the process.

Short Answer

Expert verified
The entropy change (ΔS) for the isothermal process where the volume of helium gas is increased from 2.00 L to 5.00 L at 300 K, is approximately \(2.071~J/K\).

Step by step solution

01

Convert temperature to Kelvin

In thermodynamics, it's crucial to use the Kelvin temperature scale. To convert the given temperature (27°C) to Kelvin, we need to add 273: T = 27°C + 273 = \(300 K\) Now, we have the temperature in Kelvin and are ready to proceed.
02

Use the formula for entropy change

We will use the formula for entropy change in an isothermal process for an ideal gas: ΔS = nR * ln(V2/V1) We have: - n = 0.100 mol - R = 8.314 J/mol K (gas constant) - V1 = 2.00 L - V2 = 5.00 L
03

Calculate the entropy change

Plug the values into the ΔS formula and calculate the entropy change: ΔS = (0.100 mol) * (8.314 J/mol K) * ln(\(5.00 L / 2.00 L\)) ΔS ≈ (0.100 mol) * (8.314 J/mol K) * ln(2.5) ΔS ≈ \(2.071~J/K\) The entropy change for the process is approximately \(2.071~J/K\).

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Most popular questions from this chapter

For each of the following pairs, choose the substance with the higher entropy per mole at a given temperature: (a) \(\operatorname{Ar}(l)\) or \(\operatorname{Ar}(g)\), (b) \(\mathrm{He}(g)\) at 3 atm pressure or \(\mathrm{He}(\mathrm{g})\) at \(1.5\) atm pressure, (c) \(1 \mathrm{~mol}\) of \(\mathrm{Ne}(g)\) in \(15.0 \mathrm{~L}\) or mol of \(\mathrm{Ne}(\mathrm{g})\) in \(1.50 \mathrm{~L}_{,}(\mathrm{d}) \mathrm{CO}_{2}(g)\) or \(\mathrm{CO}_{2}(\mathrm{~s})\)

For the majority of the compounds listed in Appendix \(C_{r}\), the value of \(\Delta G_{f}^{\circ}\) is more positive (or less negative) than the value of \(\Delta H_{f}^{\circ}\) (a) Explain this observation, using \(\mathrm{NH}_{3}(\mathrm{~g}), \mathrm{CCl}_{4}(l)\), and \(\mathrm{KNO}_{3}(s)\) as examples. (b) An exception to this observation is \(\mathrm{CO}(g)\). Explain the trend in the \(\Delta H_{f}^{\circ}\) and \(\Delta G_{f}^{\circ}\) values for this molecule.

Thenormal boiling point of methanol \(\left(\mathrm{CH}_{3} \mathrm{OH}\right)\) is \(64.7^{\circ} \mathrm{C}\), and its molar enthalpy of vaporization is \(\Delta H_{\mathrm{vap}}=\) \(71.8 \mathrm{~kJ} / \mathrm{mol} .\) (a) When \(\mathrm{CH}_{3} \mathrm{OH}(l)\) boils at its normal boiling point, does its entropy increase or decrease? (b) Calculate the value of \(\Delta S\) when \(1.00\) mol of \(\mathrm{CH}_{3} \mathrm{OH}(t)\) is vaporized at \(64.7^{\circ} \mathrm{C}\).

The reaction $$ \mathrm{SO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{~S}(g) \rightleftharpoons 3 \mathrm{~S}(s)+2 \mathrm{H}_{2} \mathrm{O}(g) $$ is the basis of a suggested method for removal of \(\mathrm{SO}_{2}\) from power-plant stack gases. The standard free energy of each substance is given in Appendix C. (a) What is the equilibrium constant for the reaction at \(298 \mathrm{~K} ?(\mathrm{~b})\) In principle, is this reaction a feasible method of removing \(\mathrm{SO}_{2} ?\) (c) If \(P_{\mathrm{SO}_{2}}=P_{\mathrm{H}_{2} \mathrm{~S}}\) and the vapor pressure of water is 25 torr, calculate the equilibrium \(\mathrm{SO}_{2}\) pressure in the system at \(298 \mathrm{~K}\). (d) Would you expect the process to be more or less effective at higher temperatures?

The value of \(K_{a}\) for nitrous acid \(\left(\mathrm{HNO}_{2}\right)\) at \(25^{\circ} \mathrm{C}\) is given in Appendix D. (a) Write the chemical equation for the equilibrium that corresponds to \(K_{a}\). (b) By using the value of \(K_{a}\) calculate \(\Delta G^{\circ}\) for the dissociation of nitrous acid in aqueous solution. (c) What is the value of \(\Delta G\) at equilibrium? (d) What is the value of \(\Delta G\) when \(\left[\mathrm{H}^{+}\right]=5.0 \times 10^{-2} \mathrm{M}\), \(\left[\mathrm{NO}_{2}^{-}\right]=6.0 \times 10^{-4} M\), and \(\left[\mathrm{HNO}_{2}\right]=0.20 \mathrm{M} ?\)

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