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From their standard reduction potentials, which of the following metals would you expect to dissolve in \({\rm{HCl}}\)by the reaction\({\rm{M}} + n{{\rm{H}}^ + } \to {{\rm{M}}^{n + }} + \frac{n}{2}{{\rm{H}}_2}:{\rm{Zn}},{\rm{Fe}},{\rm{Co}},{\rm{Al}},{\rm{Hg}},{\rm{Cu}},{\rm{Pt}}\),\({\bf{Au}}\)?

(When the potential predicts that the element will not dissolve, it probably will not. If it is expected to dissolve, it may dissolve if some other process does not interfere. Predictions based on standard reduction potentials at \({\bf{2}}{{\bf{5}}^{^{\bf{o}}}}C\) are only tentative, because the potentials and activities in hot, concentrated solutions vary widely from those in the table of standard potentials.)

Short Answer

Expert verified

\({\rm{Zn,}}\)\({\rm{Fe}},{\rm{Co}}\)and\({\rm{Al}}\) are dissolved in HCl because the reduction potentials of these metals are less than HCl. Thus they can reduce hydrogen and get dissolved in HCl.

Step by step solution

01

Definition of Hydrochloric acid.

Hydrochloric acid is a strong acid. It dissociates into \({{\rm{H}}^{\rm{ + }}}\,{\rm{and}}\,\,{\rm{C}}{{\rm{l}}^{\rm{ - }}}\) in aqueous solution.

\({\rm{HCl}}\,{\rm{ + }}{{\rm{H}}_{\rm{2}}}{\rm{O}} \to {{\rm{H}}_{\rm{3}}}{{\rm{O}}^{\rm{ + }}}{\rm{ + C}}{{\rm{l}}^{\rm{ - }}}\)

02

Determine the metals that dissolve in \({\rm{HCl}}\)by the reaction

  • In this task we will determine which of the following metals ( \({\rm{Zn}},{\rm{Fe}},{\rm{Co}},{\rm{Al}},{\rm{Hg}},{\rm{Cu}},{\rm{Pt}}\) or \({\rm{Au}}\)) would we expect to dissolve in \({\rm{HCl}}\), from their standard reduction potentials by the reaction:
  • When a metal reacts with \({\rm{HCl}}\)the hydrogen gets reduced from oxidation state +1 to oxidation state 0. Thus hydrogen gets reduced and the metal gets oxidized.
  • \({\rm{M}} + n{{\rm{H}}^ + } \to {{\rm{M}}^{2 + }} + \frac{n}{2}{{\rm{H}}_2}\)
  • The standard reduction potential for the reduction of hydrogen is zero.
  • \({\rm{2}}{{\rm{H}}^{\rm{ + }}}{\rm{ + 2}}{{\rm{e}}^{\rm{ - }}} \to {{\rm{H}}_{\rm{2}}}\)\({{\rm{E}}_{{{\rm{H}}^{\rm{ + }}}{\rm{/}}{{\rm{H}}_{\rm{2}}}}} = 0.0\)
  • So hydrogen can be reduced by only those metals whose standard reduction potential is less than zero. The elements having negative reduction potential are Fe, Co, Al and Zn. Therefore, these metals can dissolve in HCl.
  • On the other hand, Hg, Cu, Pt and Au have positive values of reduction potential. Thus, they cannot reduce hydrogen and cannot get dissolved in HCl.

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Most popular questions from this chapter

Barium titanate, a ceramic used in electronics, was analyzed by the following procedure: Into a Pt crucible was placed \(1.2\;{\rm{g}}\)of \({\rm{N}}{{\rm{a}}_2}{\rm{C}}{{\rm{O}}_3}\) and \(0.8\;{\rm{g}}\)of \({\rm{N}}{{\rm{a}}_2}\;{{\rm{B}}_4}{{\rm{O}}_7}\)plus \(0.3146\;{\rm{g}}\)of unknown. After fusion at \({1000^\circ }{\rm{C}}\)in a furnace for\(30\;{\rm{min}}\), the cooled solid was extracted with \(50\;{\rm{mL}}\)of\(6{\rm{MHCl}}\), transferred to a \(100 - {\rm{mL}}\) volumetric flask, and diluted to the mark. A \(25.00 - {\rm{mL}}\)aliquot was treated with \(5\;{\rm{mL}}\)of \(15\% \)tartaric acid (which complexes \({\rm{T}}{{\rm{i}}^{4 + }}\)and keeps it in aqueous solution) and \(25\;{\rm{mL}}\)of ammonia buffer,\({\rm{pH}}9.5\). The solution was treated with organic reagents that complex\({\rm{B}}{{\rm{a}}^{2 + }}\), and the \({\rm{Ba}}\)complex was extracted into \({\rm{CC}}{{\rm{l}}_4}.\)After acidification (to release the \({\rm{B}}{{\rm{a}}^{2 + }}\) from its organic complex), the \({\rm{B}}{{\rm{a}}^{2 + }}\)was backextracted into\(0.1{\rm{MHCl}}\). The final aqueous sample was treated with ammonia buffer and methylthymol blue (a metal ion indicator) and titrated with \(32.49\;{\rm{mL}}\) of \(0.01144{\rm{M}}\)EDTA. Find the weight per cent of Ba in the ceramic.

Why is it advantageous to use large particles \(\left( {{\bf{50}}{\rm{ }}\mu {\bf{m}}} \right)\) for solid phase extraction, but small particles \(\left( {{\bf{5}}{\rm{ }}\mu {\bf{m}}} \right)\) for chromatography?

Acid-base equilibria of Cr(III) were summarized in Problem 10-36. Cr(VI) in aqueous solution above pH 6 exists as the yellow tetrahedral chromate ion, \({\rm{CrO}}_4^{2 - }.\)Between\({\rm{pH}}2\)and \(6,{\rm{Cr}}\)(VI) exists as an equilibrium mixture of\({\rm{HCrO}}_4^ - \) and orange-red dichromate,\({\rm{C}}{{\rm{r}}_2}{\rm{O}}_7^{2 - }.{\rm{Cr}}({\rm{VI}})\) is a carcinogen, but \({\rm{Cr }}(III)\)is not considered to be as harmful. The following procedure was used to measure\({\rm{Cr }}({\rm{VI}})\) in airborne particulate matter in workplaces.

1. Particles were collected by drawing a known volume of air through a polyvinyl chloride filter with \(5 - \mu {\rm{M}}\)pore size.

2. The filter was placed in a centrifuge tube and \(10\;{\rm{mL}}\)of \(0.05{\rm{M}}{\left( {{\rm{N}}{{\rm{H}}_4}} \right)_2}{\rm{S}}{{\rm{O}}_4}/0.05{\rm{MN}}{{\rm{H}}_3}buffer,{\rm{pH}}8,\) were added. The immersed filter was agitated by ultrasonic vibration for\(30\;{\rm{min}}\)at \({35^\circ }{\rm{C}}\)to extract all \({\rm{Cr }}(III)and{\rm{Cr}}\)(VI) into solution.

3. A measured volume of extract was passed through a "strongly basic" anion exchanger (Table 26-1) in the \({\rm{C}}{{\rm{l}}^ - }\)form. Then the resin was washed with distilled water. Liquid containing \({\rm{Cr}}\)(III) from the extract and the wash was discarded.

4. Cr(VI) was then eluted from the column with\(0.5{\rm{M}}{\left( {{\rm{N}}{{\rm{H}}_4}} \right)_2}{\rm{S}}{{\rm{O}}_4}/0.05{\rm{MN}}{{\rm{H}}_3}\) buffer, \({\rm{pH}}8,\)and collected in a vial.

5. The eluted \({\rm{Cr}}\)(VI) solution was acidified with \({\rm{HCl}}\)and treated with a solution of 1,5 -diphenylcarbazide, a reagent that forms a colored complex with Cr(VI). The concentration of the complex was measured by its visible absorbance.

(a) What are the dominant species of \({\rm{Cr}}\)(VI) and \({\rm{Cr}}\)(III) at\({\rm{pH}}8\)?

(b) What is the purpose of the anion exchanger in step 3 ?

(c) Why is a "strongly basic" anion exchanger used instead of a "weakly basic" exchanger?

(d) Why is Cr(VI) eluted in step 4 but not step 3 ?

By what factor must the mass increase to reduce the sampling standard deviation by a factor of 2?

The county landfill in the diagram was monitored to verify that toxic compounds were not leaching into the local water supply. Wells drilled at 21 locations were monitored over a year and pollutants were observed only at sites\(8,11,12\), and 13 . Monitoring all 21 sites each month is very expensive. Suggest a strategy to use composite samples (Box 0-1) made from more than one well at a time to reduce the cost of routine monitoring. How will your scheme affect the minimum detectable level for pollutants at a particular site?

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