At what temperatures will the following processes be spontaneous? a. \(\Delta H=-18 \mathrm{kJ}\) and \(\Delta S=-60 . \mathrm{J} / \mathrm{K}\) b. \(\Delta H=+18 \mathrm{kJ}\) and \(\Delta S=+60 . \mathrm{JK}\) c. \(\Delta H=+18 \mathrm{kJ}\) and \(\Delta S=-60 . \mathrm{J} / \mathrm{K}\) d. \(\Delta H=-18 \mathrm{kJ}\) and \(\Delta S=+60 . \mathrm{J} / \mathrm{K}\)

Short Answer

Expert verified
The processes will be spontaneous at the following temperatures: a. \(T > 300 \mathrm{K}\) b. Never spontaneous c. Never spontaneous d. Spontaneous at all temperatures

Step by step solution

01

Convert the enthalpy and entropy values to the same units

We have the given enthalpy in kJ and the given entropy in J/K. We need to convert them to the same units, so let's convert the enthalpy from kJ to J: \[\Delta H = -18 \mathrm{kJ} \times 1000 = -18000 \mathrm{J}\]
02

Substitute values into the Gibbs free energy formula and solve for temperature

Plug the given values of \(\Delta H\) and \(\Delta S\) into the Gibbs free energy formula and solve for \(T\) when \(\Delta G < 0\): \[\Delta G = \Delta H - T\Delta S\] \[0 > -18000 \mathrm{J} - T(-60 \mathrm{J} / \mathrm{K})\] To find the temperature range for spontaneity, divide both sides by 60 J/K: \[T > \frac{18000}{60} = 300\mathrm{K}\] So, the process will be spontaneous at temperatures greater than 300 K. #b. \(\Delta H=+18 \mathrm{kJ}\) and \(\Delta S=+60 . \mathrm{J} / \mathrm{K}\)
03

Convert the enthalpy and entropy values to the same units

We have the given enthalpy in kJ and the given entropy in J/K. We need to convert them to the same units, so let's convert the enthalpy from kJ to J: \[\Delta H = 18 \mathrm{kJ} \times 1000 = 18000 \mathrm{J}\]
04

Substitute values into the Gibbs free energy formula and solve for temperature

Plug the given values of \(\Delta H\) and \(\Delta S\) into the Gibbs free energy formula and solve for \(T\) when \(\Delta G < 0\): \[\Delta G = \Delta H - T\Delta S\] \[0 > 18000 \mathrm{J} - T(60 \mathrm{J} / \mathrm{K})\] To find the temperature range for spontaneity, divide both sides by 60 J/K: \[T > \frac{-18000}{60} = -300\mathrm{K}\] Since the temperature cannot be negative, this process is never spontaneous. #c. \(\Delta H=+18 \mathrm{kJ}\) and \(\Delta S=-60 . \mathrm{J} / \mathrm{K}\) For this process, both \(\Delta H\) and \(\Delta S\) have positive and negative values, respectively. Since an increase in the temperature would amplify the negative effect of \(\Delta S\) and worsen the positive \(\Delta H\) value, this process will never be spontaneous at any temperature. #d. \(\Delta H=-18 \mathrm{kJ}\) and \(\Delta S=+60 . \mathrm{J} / \mathrm{K}\) The given values for \(\Delta H\) and \(\Delta S\) are the same as in part a, but \(\Delta S\) is positive. As \(\Delta H\) is negative and \(\Delta S\) is positive, the process will be spontaneous at all temperatures, as the Gibbs free energy will always be negative.

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Most popular questions from this chapter

Which of the following reactions (or processes) are expected to have a negative value for \(\Delta S^{\circ} ?\) a. $\mathrm{SiF}_{6}(a q)+\mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{HF}(g)+\mathrm{SiF}_{4}(g)$ b. $4 \mathrm{Al}(s)+3 \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{Al}_{2} \mathrm{O}_{3}(s)$ c. \(\mathrm{CO}(g)+\mathrm{Cl}_{2}(g) \longrightarrow \mathrm{COCl}_{2}(g)\) d. $\mathrm{C}_{2} \mathrm{H}_{4}(g)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)$ e. \(\mathrm{H}_{2} \mathrm{O}(s) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)\)

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