The normal boiling point of \(\mathrm{Br}_{2}(l)\) is \(58.8^{\circ} \mathrm{C},\) and its molar enthalpy of vaporization is \(\Delta H_{\mathrm{vap}}=29.6 \mathrm{kJ} / \mathrm{mol}\) (a) When \(\mathrm{Br}_{2}(l)\) boils at its normal boiling point, does its entropy increase or decrease? (b) Calculate the value of \(\Delta S\) when 1.00 mol of \(\mathrm{Br}_{2}(l)\) is vaporized at \(58.8^{\circ} \mathrm{C}\) .

Short Answer

Expert verified
During the boiling of Br2(l) at its normal boiling point, the entropy increases. The entropy change (∆S) when 1.00 mol of Br2(l) is vaporized at 58.8°C is 89.1 J/(mol·K).

Step by step solution

01

Part (a): Determining if Entropy Increases or Decreases

When a substance undergoes a phase change, such as boiling, the particles become more disordered and more dispersed. In the case of liquid bromine boiling and becoming gaseous bromine, the increased freedom of movement and spacing between the particles contribute to a higher entropy, which is a measure of disorder in a system. Thus, during the boiling of Br2(l) at its normal boiling point, the entropy increases.
02

Part (b): Calculate the Entropy Change (∆S)

Next, we calculate the entropy change (∆S) when 1.00 mol of Br2(l) is vaporized at its boiling point. We use the equation: \(\Delta S = \frac{\Delta H_{vap}}{T}\) We are given the molar enthalpy of vaporization \(\Delta H_{vap} = 29.6 \, kJ/mol\) and the boiling point temperature \(T = 58.8^{\circ} C\). First, we need to convert the temperature from Celsius to Kelvin: \(T_{(K)} = T_{(C)} + 273.15\) \(T_{(K)} = 58.8 + 273.15 = 331.95\,K\) Now, we apply the equation: \(\Delta S = \frac{29.6 \, kJ/mol}{331.95 \, K}\) Note that we need to convert kJ to J by multiplying with 1000: \(\Delta S = \frac{29.6 \times 1,000\, J/mol}{331.95 \, K} = 89.1\frac{J}{mol \cdot K}\) Therefore, the entropy change, ∆S, when 1.00 mol of Br2(l) is vaporized at its normal boiling point is 89.1 J/(mol·K).

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Most popular questions from this chapter

Consider a process in which an ideal gas changes from state 1 to state 2 in such a way that its temperature changes from 300 K to 200 K. (a) Does the temperature change depend on whether the process is reversible or irreversible? (b) Is this process isothermal? (c) Does the change in the internal energy, \(\Delta E,\) depend on the particular pathway taken to carry out this change of state?

An ice cube with a mass of 20 \(\mathrm{g}\) at \(-20^{\circ} \mathrm{C}\) (typical freezer temperature) is dropped into a cup that holds 500 \(\mathrm{mL}\) of hot water, initially at \(83^{\circ} \mathrm{C} .\) What is the final temperature in the cup? The density of liquid water is 1.00 \(\mathrm{g} / \mathrm{mL}\) ; the specific heat capacity of ice is \(2.03 \mathrm{J} / \mathrm{g}-\mathrm{C}\) ; the specific heat capacity of liquid water is \(4.184 \mathrm{J} / \mathrm{g}-\mathrm{C} ;\) the enthalpy of fusion of water is 6.01 \(\mathrm{k} \mathrm{J} / \mathrm{mol} .\)

Trouton's rule states that for many liquids at their normal boiling points, the standard molar entropy of vaporization is about \(88 \mathrm{J} / \mathrm{mol}-\mathrm{K}\) (a) Estimate the normal boiling point of bromine, \(\mathrm{Br}_{2},\) by determining \(\Delta H_{\mathrm{vap}}^{\circ}\) for \(\mathrm{Br}_{2}\) using data from Appendix C. Assume that \(\Delta H_{\text { vap }}^{\circ}\) remains constant with temperature and that Trouton's rule holds. (b) Look up the normal boiling point of \(B r_{2}\) in a chemistry handbook or at the WebElements website (www..webelements.com) and compare it to your calculation. What are the possible sources of error, or incorrect assumptions, in the calculation?

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From the values given for \(\Delta H^{\circ}\) and \(\Delta S^{\circ},\) calculate \(\Delta G^{\circ}\) for each of the following reactions at 298 \(\mathrm{K}\) . If the reaction is not spontaneous under standard conditions at 298 \(\mathrm{K}\) , at what temperature (if any) would the reaction become spontaneous? $$ \begin{array}{l}{\text { (a) } 2 \mathrm{PbS}(s)+3 \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{PbO}(s)+2 \mathrm{SO}_{2}(g)} \\ {\Delta H^{\circ}=-844 \mathrm{kk} ; \Delta S^{\circ}=-165 \mathrm{J} / \mathrm{K}} \\\ {\text { (b) } 2 \mathrm{POCl}_{3}(g) \longrightarrow 2 \mathrm{PCl}_{3}(g)+\mathrm{O}_{2}(g)} \\ {\Delta H^{\circ}=572 \mathrm{kJ} ; \Delta S^{\circ}=179 \mathrm{J} / \mathrm{K}}\end{array} $$

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