Suggest how the cations in each of the following solution mixtures can be separated: (a) \(\mathrm{Na}^{+}\) and $\mathrm{Cd}^{2+},(\mathbf{b}) \mathrm{Cu}^{2+}\( and \)\mathrm{Mg}^{2+},(\mathbf{c}) \mathrm{Pb}^{2+}$ and \(\mathrm{Al}^{3+},(\mathbf{d}) \mathrm{Ag}^{+}\) and \(\mathrm{Hg}^{2+} .\)

Short Answer

Expert verified
To separate the cations in each solution mixture: (a) Add sodium sulfide (Na2S) to form insoluble cadmium sulfide (CdS) precipitate, filter it out, leaving Na+ in the solution. (b) Add excess ammonia to form soluble [Cu(NH3)4]2+ complex ion, separate it, and recover Cu2+ and Mg2+ ions from their complexes and salts. (c) Add sodium hydroxide (NaOH) to form insoluble lead hydroxide (Pb(OH)2) precipitate, filter it out, and recover Al3+ and Pb2+ ions from their respective hydroxide salts. (d) Add sodium chloride (NaCl) to form insoluble silver chloride (AgCl) and mercury(I) chloride (Hg2Cl2) precipitates, separate them using ammonia, and recover Ag+ and Hg2+ ions from their respective chloride salts.

Step by step solution

01

(a) Separating Na+ and Cd2+ ions

To separate Na+ and Cd2+ ions from a solution mixture, we can take advantage of the difference in solubility of their respective sulfide salts. Step 1: Add a source of sulfide ions, such as sodium sulfide (Na2S), to the solution containing the Na+ and Cd2+ ions. This will cause the formation of insoluble cadmium sulfide (CdS) in the presence of Cd2+ ions while sodium sulfide (Na2S) will remain soluble in the solution. Step 2: Filter out the cadmium sulfide (CdS) precipitate, which will separate the Cd2+ ions from the solution. The remaining solution will contain Na+ ions. Step 3: If necessary, evaporate the water from the remaining solution to obtain solid sodium ions in the form of a sodium salt, such as sodium chloride (NaCl).
02

(b) Separating Cu2+ and Mg2+ ions

To separate Cu2+ and Mg2+ ions from a solution mixture, we can make use of the difference in their complexation tendencies with ammonia (NH3). Step 1: Add excess ammonia solution to the solution containing Cu2+ and Mg2+ ions. This will cause the Cu2+ ions to form a soluble complex ion, [Cu(NH3)4]2+, while Mg2+ ions will remain as free ions in the solution. Step 2: Separate the [Cu(NH3)4]2+ complex ion from the Mg2+ ions by filtration, if there is a change in color or a formation of a precipitate. In some cases, you may need to use an ion-exchange column to perform this separation step. Step 3: If necessary, recover the Cu2+ and Mg2+ ions from their respective complexes and salts by evaporating the water or by performing a chemical reaction that releases the free metal ions.
03

(c) Separating Pb2+ and Al3+ ions

To separate Pb2+ and Al3+ ions from a solution mixture, we can use the difference in solubility of their hydroxide salts. Step 1: Add a concentrated solution of sodium hydroxide (NaOH) to the solution containing Pb2+ and Al3+ ions. This will cause the formation of insoluble lead hydroxide, Pb(OH)2, while aluminum hydroxide, Al(OH)3, will remain soluble in the solution. Step 2: Filter out the lead hydroxide (Pb(OH)2) precipitate, which will separate the Pb2+ ions from the solution. The remaining solution will contain Al3+ ions. Step 3: If necessary, recover the Al3+ and Pb2+ ions from their respective hydroxide salts by performing a chemical reaction that releases the free metal ions, such as by acidification with hydrochloric acid (HCl).
04

(d) Separating Ag+ and Hg2+ ions

To separate Ag+ and Hg2+ ions from a solution mixture, we can utilize the difference in solubility of their chloride salts. Step 1: Add a solution of sodium chloride (NaCl) to the solution containing Ag+ and Hg2+ ions. This will cause the formation of insoluble silver chloride (AgCl) and insoluble mercury(I) chloride (Hg2Cl2). Step 2: Filter out the silver chloride (AgCl) and mercury(I) chloride (Hg2Cl2) precipitates, which will separate the Ag+ and Hg2+ ions from the solution. Step 3: To separate AgCl from Hg2Cl2, add aqueous ammonia solution to the mixture of the two precipitates. This will cause the AgCl to dissolve into [Ag(NH3)2]+ complex ion, while Hg2Cl2 will remain insoluble. Filter out the insoluble Hg2Cl2. Step 4: If necessary, recover the Ag+ and Hg2+ ions from their respective chloride salts by performing a chemical reaction that releases the free metal ions, such as by acidification with nitric acid (HNO3).

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Most popular questions from this chapter

A buffer contains 0.30 mol of propionic acid $\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{COOH}\right)\( and \)0.25 \mathrm{~mol}$ of potassium propionate \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{COOK}\right)\) in 1.80 L. (a) What is the pH of this buffer? (b) What is the pH of the buffer after the addition of \(0.10 \mathrm{~mol}\) of \(\mathrm{NaOH}\) ? \((\mathbf{c})\) What is the \(\mathrm{pH}\) of the buffer after the addition of \(0.10 \mathrm{~mol}\) of \(\mathrm{HCl}\) ?

Derive an equation similar to the Henderson-Hasselbalch equation relating the pOH of a buffer to the \(\mathrm{pK}_{b}\) of its base component.

Two buffers are prepared by adding an equal number of moles of formic acid (HCOOH) and sodium formate (HCOONa) to enough water to make \(1.00 \mathrm{~L}\) of solution. Buffer A is prepared using 1.00 mol each of formic acid and sodium formate. Buffer B is prepared by using 0.010 mol of each. (a) Calculate the pH of each buffer. (b) Which buffer will have the greater buffer capacity? (c) Calculate the change in \(\mathrm{pH}\) for each buffer upon the addition of \(1.0 \mathrm{~mL}\) of \(1.00 \mathrm{MHCl}\). (d) Calculate the change in \(\mathrm{pH}\) for each buffer upon the addition of \(10 \mathrm{~mL}\) of $1.00 \mathrm{MHCl}$.

(a) Calculate the pH of a buffer that is \(0.150 \mathrm{M}\) in lactic acid and \(0.120 M\) in sodium lactate. (b) Calculate the pH of a buffer formed by mixing \(75 \mathrm{~mL}\) of \(0.150 \mathrm{M}\) lactic acid with \(25 \mathrm{~mL}\) of \(0.120 \mathrm{M}\) sodium lactate.

Consider the titration of \(30.0 \mathrm{~mL}\) of $0.050 \mathrm{M} \mathrm{NH}_{3}\( with \)0.025 M$ HCl. Calculate the pH after the following volumes of titrant have been added: $(\mathbf{a}) 0 \mathrm{~mL},(\mathbf{b}) 20.0 \mathrm{~mL},\( (c) 59.0 \)\mathrm{mL},(\mathbf{d}) 60.0 \mathrm{~mL},(\mathbf{e}) 61.0 \mathrm{~mL},(\mathbf{f}) 65.0 \mathrm{~mL} .$

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