Some nonelectrolyte solute (molar mass \(=142 \mathrm{g} / \mathrm{mol} )\) was dissolved in \(150 . \mathrm{mL}\) of a solvent (density $=0.879 \mathrm{g} / \mathrm{cm}^{3} )$ The elevated boiling point of the solution was 355.4 \(\mathrm{K}\) . What mass of solute was dissolved in the solvent? For the solvent, the enthalpy of vaporization is 33.90 \(\mathrm{kJ} / \mathrm{mol}\) , the entropy of vaporization is 95.95 \(\mathrm{J} / \mathrm{K} \cdot\) mol, and the boiling- point elevation constant is 2.5 \(\mathrm{K} \cdot \mathrm{kg} / \mathrm{mol}\) .

Short Answer

Expert verified
The mass of the solute dissolved in the solvent is \(16.79\ \mathrm{g}\).

Step by step solution

01

Calculate the boiling-point elevation

The boiling-point elevation can be calculated using the formula: \(\Delta T_b = K_b \cdot m\) where \(\Delta T_b\) is the boiling-point elevation, \(K_b\) is the boiling-point elevation constant, and \(m\) is the molality of the solute in the solution. We are given the boiling-point elevation constant, \(K_b = 2.5\ \mathrm{K} \cdot \mathrm{kg} / \mathrm{mol}\), and the boiling point of the solution, \(T_{solution} = 355.4\ \mathrm{K}\). First, we find the normal boiling point of the solvent, \(T_{solvent}\), using the given values of enthalpy and entropy of vaporization: \(T_{solvent}=\frac{\Delta H_v}{\Delta S_v}\) where \(\Delta H_v = 33.90\ \mathrm{kJ} / \mathrm{mol} = 33900\ \mathrm{J} / \mathrm{mol}\) and \(\Delta S_v = 95.95\ \mathrm{J} / \mathrm{K} \cdot \mathrm{mol}\). \(T_{solvent}=\frac{33900\ \mathrm{J} / \mathrm{mol}}{95.95\ \mathrm{J} / \mathrm{K} \cdot \mathrm{mol}} = 353.16\ \mathrm{K}\) Now, we can find the boiling-point elevation: \(\Delta T_b = T_{solution} - T_{solvent} = 355.4\ \mathrm{K} - 353.16\ \mathrm{K} = 2.24\ \mathrm{K}\)
02

Calculate the molality of the solute

Now that we have the boiling-point elevation, we can calculate the molality of the solute using the formula: \(m=\frac{\Delta T_b}{K_b}\) \(m=\frac{2.24\ \mathrm{K}}{2.5\ \mathrm{K} \cdot \mathrm{kg} / \mathrm{mol}}=0.896 \ \mathrm{mol} / \mathrm{kg}\)
03

Calculate the mass of the solvent

To calculate the mass of the solvent, we use the given volume and density of the solvent. Mass of solvent = Volume × Density where Volume = \(150\ \mathrm{mL} = 0.150\ \mathrm{L}\) and Density = \(0.879\ \mathrm{g} / \mathrm{cm}^{3}\). To convert volume from liters to cubic centimeters, we can multiply by 1000. Volume in cubic centimeters = \(0.150\ \mathrm{L} \times 1000 = 150\ \mathrm{cm}^{3}\) Now, we can find the mass of the solvent: Mass of solvent = \(150\ \mathrm{cm}^{3} \times 0.879\ \mathrm{g} / \mathrm{cm}^{3} = 131.85\ \mathrm{g}\)
04

Calculate the mass of the solute

Now that we know the molality of the solute and the mass of the solvent, we can find the moles of solute using the formula: moles of solute = \(\frac{m \times \text{Mass of solvent}}{\text{Molar mass of solvent}}\) Moles of solute = \(\frac{0.896\ \mathrm{mol} / \mathrm{kg} \times 131.85\ \mathrm{g}}{1000\ \mathrm{g}/\mathrm{kg}} = 0.1182\ \mathrm{mol}\) Finally, we find the mass of the solute using the given molar mass of the solute, \(M = 142\ \mathrm{g} / \mathrm{mol}\). Mass of solute = moles of solute × molar mass of solute Mass of solute = \(0.1182\ \mathrm{mol} \times 142\ \mathrm{g} / \mathrm{mol} = 16.79\ \mathrm{g}\) So, the mass of solute dissolved in the solvent is 16.79 g.

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Most popular questions from this chapter

As \(\mathrm{O}_{2}(l)\) is cooled at \(1 \mathrm{atm},\) it freezes at 54.5 \(\mathrm{K}\) to form solid I. At a lower temperature, solid I rearranges to solid II, which has a different crystal structure. Thermal measurements show that \(\Delta H\) for the $I \rightarrow\( II phase transition is \)-743.1 \mathrm{J} / \mathrm{mol}$ , and \(\Delta S\) for the same transition is \(-17.0 \mathrm{J} / \mathrm{K} \cdot\) mol. At what temperature are solids I and II in equilibrium?

The melting point for carbon diselenide \(\left(\mathrm{CSe}_{2}\right)\) is \(-46^{\circ} \mathrm{C}\) . At a temperature of \(-75^{\circ} \mathrm{C},\) predict the signs for \(\Delta S_{\mathrm{surr}}\) and $\Delta S_{\mathrm{univ}}\( for the following process: \)\operatorname{CSe}_{2}(l) \rightarrow \operatorname{CSe}_{2}(s)$

Consider a weak acid, HX. If a \(0.10-M\) solution of \(\mathrm{HX}\) has a pH of 5.83 at \(25^{\circ} \mathrm{C},\) what is \(\Delta G^{\circ}\) for the acid's dissociation reaction at \(25^{\circ} \mathrm{C} ?\)

Consider the dissociation of a weak acid $\mathrm{HA}\left(K_{\mathrm{a}}=4.5 \times 10^{-3}\right)$ in water: $$\mathrm{HA}(a q) \rightleftharpoons \mathrm{H}^{+}(a q)+\mathrm{A}^{-}(a q)$$ Calculate \(\Delta G^{\circ}\) for this reaction at \(25^{\circ} \mathrm{C}\)

Impure nickel, refined by smelting sulfide ores in a blast furnace, can be converted into metal from 99.90% to 99.99% purity by the Mond process. The primary reaction involved in the Mond process is $$\mathrm{Ni}(s)+4 \mathrm{CO}(g) \rightleftharpoons \mathrm{Ni}(\mathrm{CO})_{4}(g)$$ a. Without referring to Appendix \(4,\) predict the sign of \(\Delta S^{\circ}\) for the above reaction. Explain. b. The spontaneity of the above reaction is temperature-dependent. Predict the sign of \(\Delta S_{\text { sum }}\) for this reaction. Explain. c. For $\mathrm{Ni}(\mathrm{CO})_{4}(g), \Delta H_{\mathrm{f}}^{\circ}=-607 \mathrm{kJ} / \mathrm{mol}\( and \)S^{\circ}=417 \mathrm{J} / \mathrm{K} \cdot \mathrm{mol}\( at 298 \)\mathrm{K}$ . Using these values and data in Appendix 4 calculate \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) for the above reaction. d. Calculate the temperature at which \(\Delta G^{\circ}=0(K=1)\) for the above reaction, assuming that \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) do not depend on temperature. e. The first step of the Mond process involves equilibrating impure nickel with \(\mathrm{CO}(g)\) and \(\mathrm{Ni}(\mathrm{CO})_{4}(g)\) at about \(50^{\circ} \mathrm{C} .\) The purpose of this step is to convert as much nickel as possible into the gas phase. Calculate the equilibrium constant for the above reaction at \(50 .^{\circ} \mathrm{C}\) f. In the second step of the Mond process, the gaseous \(\mathrm{Ni}(\mathrm{CO})_{4}\) is isolated and heated to $227^{\circ} \mathrm{C}$ . The purpose of this step is to deposit as much nickel as possible as pure solid (the reverse of the preceding reaction). Calculate the equilibrium constant for the preceding reaction at \(227^{\circ} \mathrm{C}\) . g. Why is temperature increased for the second step of the Mond process? h. The Mond process relies on the volatility of \(\mathrm{Ni}(\mathrm{CO})_{4}\) for its success. Only pressures and temperatures at which \(\mathrm{Ni}(\mathrm{CO})_{4}\) is a gas are useful. A recently developed variation of the Mond process carries out the first step at higher pressures and a temperature of \(152^{\circ} \mathrm{C}\) . Estimate the maximum pressure of \(\mathrm{Ni}(\mathrm{CO})_{4}(g)\) that can be attained before the gas will liquefy at \(152^{\circ} \mathrm{C}\) . The boiling point for Nic CO) is \(42^{\circ} \mathrm{C}\) and the enthalpy of vaporization is 29.0 \(\mathrm{kJ} / \mathrm{mol} .\) [Hint: The phase change reaction and the corresponding equilibrium expression are $\mathrm{Ni}(\mathrm{CO})_{4}(l) \rightleftharpoons \mathrm{Ni}(\mathrm{CO})_{4}(g) \quad K=P_{\mathrm{NiCO} 4}$ greater than the \(K\) value. \(]\)

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