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A student is asked to prepare a \(0.030 \mathrm{M}\) aqueous solu- $$ \text { tion of } \mathrm{PbCl}_{2} $$ (a) Is this possible at \(25^{\circ} \mathrm{C}\) ? (Hint: Is dissolving \(0.030 \mathrm{~mol}\) of \(\mathrm{PbCl}_{2}\) at \(25^{\circ} \mathrm{C}\) possible?) (b) If the student used water at \(100^{\circ} \mathrm{C},\) would this be possible?

Short Answer

Expert verified
Short answer: It's not possible to prepare a 0.030 M solution of PbCl₂ at 25°C because the solubility of PbCl₂ at this temperature is only 0.0061 M. At 100°C, solubility might be higher, but without knowing the exact Ksp value, we cannot definitively determine if it's possible to prepare a 0.030 M solution at this temperature.

Step by step solution

01

Given information

We are given the following data: - A student needs to prepare 0.030 M aqueous solution of PbCl₂ - Temperature 1: 25°C - Temperature 2: 100°C Ksp of PbCl₂ at 25°C = \(1.7\times10^{-5}\)
02

Write the solubility product expression

The balanced equation for the dissolution of PbCl₂ in water is: \(\ce{PbCl2(s) <=> Pb^{2+}(aq) + 2Cl^-(aq)}\) The solubility product expression, Ksp, is given by: Ksp = [Pb²⁺][Cl⁻]²\
03

Calculate the solubility of PbCl₂ at 25°C

Let the solubility of PbCl₂ at 25°C be S. When PbCl₂ dissolves, the concentration of Pb²⁺ will be S, and the concentration of Cl⁻ will be 2S. Using the solubility product expression: Ksp = [Pb²⁺][Cl⁻]² → \(1.7\times10^{-5}\) = S(2S)² Solving the equation for S: S₃ = \(\frac{1.7\times10^{-5}}{4}\) S = \(0.0061 M\) The solubility of PbCl₂ at 25°C is 0.0061 M.
04

Determine if it's possible to prepare the solution at 25°C

The solubility of PbCl₂ at 25°C is 0.0061 M. Since the student needs to prepare a 0.030 M solution, it's not possible to dissolve enough PbCl₂ at 25°C. Answer (a): No, it's not possible to prepare a 0.030 M solution of PbCl₂ at 25°C.
05

Solubility at 100°C

We are not provided with the Ksp value for PbCl₂ at 100°C. However, in general, the solubility of salts increases with temperature as the dissolution process is often an endothermic reaction. Answer (b): Without knowing the exact Ksp value for PbCl₂ at 100°C, we cannot definitively determine if it's possible to prepare a 0.030 M solution. However, solubility may be higher at this temperature, so there is a possibility, but it's not guaranteed.

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Most popular questions from this chapter

Calculate \(\Delta G^{\circ}\) at \(82^{\circ} \mathrm{C}\) for reactions in which (a) \(\Delta H^{\circ}=293 \mathrm{~kJ} ; \quad \Delta S^{\circ}=-695 \mathrm{~J} / \mathrm{K}\) (b) \(\Delta H^{\circ}=-1137 \mathrm{~kJ} ; \quad \Delta S^{\circ}=0.496 \mathrm{~kJ} / \mathrm{K}\) (c) \(\Delta H^{\circ}=-86.6 \mathrm{~kJ} ; \quad \Delta S^{\circ}=-382 \mathrm{~J} / \mathrm{K}\)

Fill in the blanks: (a) \(\Delta H^{\circ}\) and \(\Delta G^{\circ}\) become equal at __________ K. (b) \(\Delta G^{\circ}\) and \(\Delta G\) are equal when \(Q=\) __________ (c) \(S^{\circ}\) for steam is __________ than \(S^{\circ}\) for water.

A \(0.250 \mathrm{M}\) solution of a weak base \(\mathrm{R}_{2} \mathrm{NH}\) has a \(\mathrm{pH}\) of 10.60 at \(25^{\circ} \mathrm{C}\). What is \(\Delta G^{\circ}\) for the dissociation of the weak base in water at \(25^{\circ} \mathrm{C}\) ? $$ \mathrm{R}_{2} \mathrm{NH}(a q)+\mathrm{H}_{2} \mathrm{O} \longrightarrow \mathrm{R}_{2} \mathrm{NH}_{2}^{+}(a q)+\mathrm{OH}^{-}(a q) $$

In your own words, explain why (a) \(\Delta S^{\circ}\) is negative for a reaction in which the number of moles of gas decreases. (b) we take \(\Delta S^{\circ}\) to be independent of \(T,\) even though entropy increases with \(T\). (c) a solid has lower entropy than its corresponding liquid.

Discuss the effect of temperature change on the spontaneity of the following reactions at 1 atm: $$ \text { (a) } \begin{aligned} \mathrm{Al}_{2} \mathrm{O}_{3}(s)+2 \mathrm{Fe}(s) \longrightarrow 2 \mathrm{Al}(s)+\mathrm{Fe}_{2} \mathrm{O}_{3}(s) \\ \Delta H^{\circ}=851.4 \mathrm{~kJ} ; & \Delta S^{\circ}=38.5 \mathrm{~J} / \mathrm{K} \end{aligned} $$ (b) \(\mathrm{N}_{2} \mathrm{H}_{4}(l) \longrightarrow \mathrm{N}_{2}+2 \mathrm{H}_{2}(g)\) $$ \Delta H^{\circ}=-50.6 \mathrm{~kJ} ; \quad \Delta S^{\circ}=0.3315 \mathrm{~kJ} / \mathrm{K} $$ (c) \(\mathrm{SO}_{3}(g) \longrightarrow \mathrm{SO}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g)\) $$ \Delta H^{\circ}=98.9 \mathrm{~kJ} ; \quad \Delta S^{\circ}=0.0939 \mathrm{~kJ} / \mathrm{K} $$

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