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Ammonium nitrate dissolves spontaneously and endothermally in water at room temperature. What can you deduce about the sign of \(\Delta S\) for this solution process?

Short Answer

Expert verified
The entropy change, \(\Delta S\), for the dissolution of ammonium nitrate in water is positive. This is because the dissolution is spontaneous and endothermic, meaning that \(\Delta G < 0\) and \(\Delta H > 0\). The positive entropy change compensates for the positive enthalpy change, resulting in a spontaneous process with an increase in disorder and dispersal of matter and energy.

Step by step solution

01

Understanding Gibbs Free Energy

In order to determine the sign of \(\Delta S\) for this process, we need to recall the relationship between enthalpy, entropy, and Gibbs free energy. The Gibbs free energy is an important thermodynamic quantity that indicates whether a process will occur spontaneously. The change in Gibbs free energy (∆G) for a process can be calculated using the following equation: \[ \Delta G = \Delta H - T\Delta S \] Where: - \(\Delta G\) is the change in Gibbs free energy - \(\Delta H\) is the change in enthalpy (heat content) - \(T\) is the temperature in Kelvin - \(\Delta S\) is the change in entropy (dispersal of matter and energy) A negative value for \(\Delta G\) means that the process occurs spontaneously, while a positive value means the process is non-spontaneous.
02

Analyzing Enthalpy Change \(\Delta H\)

We are given that the dissolution of ammonium nitrate in water is an endothermic process. By definition, an endothermic process means that it absorbs heat, and so the enthalpy change, \(\Delta H\), is positive.
03

Analyzing Spontaneity and Gibbs Free Energy

We are also given that the dissolution is spontaneous. This means that the Gibbs free energy change, \(\Delta G\), must be negative.
04

Determining the Sign of Entropy Change, \(\Delta S\)

Finally, we are ready to determine the sign of entropy change, \(\Delta S\). We can rearrange the Gibbs free energy equation: \[ \Delta G = \Delta H - T\Delta S \] Since we know that \(\Delta G < 0\) (spontaneous) and \(\Delta H > 0\) (endothermic), the only way to satisfy the equation is if \(\Delta S\) is positive: \[ \Delta G = (+) - T(+) \implies (-) = (-)\] In other words, the positive entropy change \(\Delta S\) compensates for the positive enthalpy change \(\Delta H\) to make the dissolution of ammonium nitrate a spontaneous process.
05

Conclusion

The entropy change, \(\Delta S\), for the dissolution of ammonium nitrate in water is positive. This positive entropy change occurs because the dissolution of ammonium nitrate leads to an increase in disorder in the system as a result of the dispersal of matter and energy.

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Most popular questions from this chapter

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.

(a) How can we calculate \(\Delta S\) foran isothermal process? (b) Does \(\Delta S\) for a process depend on the path taken from the initial to the final state of the system? Explain.

The pressure on \(0.850\) mol of neon gas is increased from \(1.25\) atm to \(2.75\) atm at \(100{ }^{\circ} \mathrm{C}\). Assuming the gas to be ideal, calculate \(\Delta S\) for this process.

(a) Express the second law of thermodynamics as a mathematical equation. (b) In a particular spontaneous process the entropy of the system decreases. What can you conclude about the sign and magnitude of \(\Delta S_{\text {surr }}\) ? (c) During a certain reversible process, the surroundings undergo an entropy change, \(\Delta S_{\text {surr }}=-78 \mathrm{~J} / \mathrm{K} .\) What is the entropy change of the system for this process?

Calculate \(\Delta S^{\circ}\) values for the following reactions by using tabulated \(S^{\circ}\) values from Appendix \(C\). In each case explain the sign of \(\Delta S^{\circ}\). (a) \(\mathrm{N}_{2} \mathrm{H}_{4}(\mathrm{~g})+\mathrm{H}_{2}(\mathrm{~g}) \longrightarrow 2 \mathrm{NH}_{3}(g)\) (b) \(\mathrm{K}(s)+\mathrm{O}_{2}(g) \longrightarrow \mathrm{KO}_{2}(s)\) (c) \(\mathrm{Mg}(\mathrm{OH})_{2}(s)+2 \mathrm{HCl}(\mathrm{g}) \longrightarrow \mathrm{MgCl}_{2}(s)+2 \mathrm{H}_{2} \mathrm{O}(l)\) (d) \(\mathrm{CO}(g)+2 \mathrm{H}_{2}(g) \longrightarrow \mathrm{CH}_{3} \mathrm{OH}(g)\)

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