Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

For the half-reaction \(\mathrm{Hg}^{2+}(\mathrm{aq})+2 \mathrm{e}^{-} \longrightarrow \mathrm{Hg}(1)\) \(E^{\circ}=0.854 \mathrm{V} .\) This means that \((\mathrm{a}) \mathrm{Hg}(1)\) is more readily oxidized than \(\mathrm{H}_{2}(\mathrm{g}) ;\) (b) \(\mathrm{Hg}^{2+}(\) aq) is more readily reduced than \(\mathrm{H}^{+}(\mathrm{aq}) ;\) (c) \(\mathrm{Hg}(\) l) will dissolve in 1 M HCl; (d) Hg(l) will displace Zn(s) from an aqueous solution of \(\mathrm{Zn}^{2+}\) ion.

Short Answer

Expert verified
(a) True, (b) True, (c) False, (d) True.

Step by step solution

01

Check if Hg(l) is more readily oxidized than H2(g)

The standard cell potential of hydrogen (E0_H2) is defined as 0V so it is less than the standard reduction potential of Hg^2+ which is 0.854V, meaning at standard conditions, Hg(l) is oxidized (loses electrons) more readily than Hg(g). So (a) is True.
02

Check if Hg^2+(aq) is more readily reduced than H+(aq)

The standard reduction potential of H+ (E0_H+) is 0V which is less than the standard reduction potential of Hg^2+ (E0_Hg) which is 0.854V, meaning at standard conditions, Hg^2+(aq) is reduced more readily than H+(aq). So (b) is True.
03

Check if Hg(l) will dissolve in 1 M HCl

Hg(l) won't dissolve in 1M HCl because Hg(l) is not easily oxidized by H+ ions whose (E0_H+) is 0V which less than the standard reduction potential of Hg^2+ (E0_Hg) which is 0.854V. So (c) is False.
04

Check if Hg(l) will displace Zn(s) from an aqueous solution of Zn^2+ ion

The standard reduction potential for Zn^2+/Zn (E0_Zn) is -0.76V which is less than the standard reduction potentials of Hg^2+/Hg (i.e., 0.854V). Thus, Hg(l) can displace Zn(s) from a solution of Zn^2+ ions since it has a higher reduction potential. So (d) is True.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Standard Electrode Potential
Standard electrode potential, denoted as \( E^{ ext{0}} \), is a critical value in electrochemistry.
It represents the voltage or electrical potential difference that can be generated by a half-cell under standard conditions when it is compared to the standard hydrogen electrode.
This potential is a measure of the tendency of a chemical species to be reduced, with higher values indicating a greater likelihood of reduction.
  • The standard electrode potential is measured in volts (V).
  • Standard conditions imply 1 M concentration for solutions, 1 atm pressure for gases, and pure solids or liquids.
  • The standard hydrogen electrode (SHE) is the reference with an \( E^{ ext{0}} \) of 0 V.
In our exercise, the half-reaction for mercury has a standard electrode potential \( (E^{ ext{0}}) \) of 0.854 V. Comparing this to the hydrogen electrode (0 V), it can be observed that \( ext{Hg}^{2+} \) ions are more easily reduced than \( ext{H}^{+} \) ions. Thus, the greater the \( E^{ ext{0}} \) value, the higher the tendency of the reduction to occur.
Redox Reactions
Redox reactions are short for reduction-oxidation reactions.
These reactions involve the transfer of electrons between chemical species.
One species will gain electrons (reduction) and another will lose electrons (oxidation).
Redox reactions are essential in many natural and industrial processes, such as:
  • Combustion
  • Respiration
  • Photosynthesis
  • Batteries and electrochemical cells
In the exercise, the redox reaction occurs between mercury and hydrogen in aqueous solutions.
Hg(l) has a higher tendency to be oxidized than hydrogen gas based on the standard electrode potentials, leading to the conclusion that when comparing these potentials, we determine the direction of electron flow.
Oxidation-Reduction
Understanding oxidation-reduction is crucial to unravel the nature of redox reactions.
In these reactions:
  • Oxidation refers to the loss of electrons by a molecule, atom, or ion.
  • Reduction is the gain of electrons by a molecule, atom, or ion.
A useful mnemonic to remember this process is "OIL RIG": Oxidation Is Loss, Reduction Is Gain.
By examining the standard electrode potentials, it is easier to predict which species will undergo oxidation and which will undergo reduction.
In the textbook exercise, mercury \( ext{Hg}(l) \) is compared to hydrogen and other species. Its higher electrode potential enables it to be reduced more readily than \( ext{H}^{+} \), but less than \( ext{Zn(s)} \).
As electrons are transferred, energy changes occur that can be harnessed in various applications like electricity generation.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

A concentration cell is constructed of two hydrogen electrodes: one immersed in a solution with \(\left[\mathrm{H}^{+}\right]=1.0 \mathrm{M}\) and the other in \(0.65 \mathrm{M} \mathrm{KOH}\) (a) Determine \(E_{\text {cell for the reaction that occurs. }}\) (b) Compare this value of \(E_{\text {cell }}\) with \(E^{\circ}\) for the reduction of \(\mathrm{H}_{2} \mathrm{O}\) to \(\mathrm{H}_{2}(\mathrm{g})\) in basic solution, and explain the relationship between them.

Ultimately, \(\Delta G_{\mathrm{f}}^{\mathrm{Q}}\) values must be based on experimental results; in many cases, these experimental results are themselves obtained from \(E^{\circ}\) values. Early in the twentieth century, G. N. Lewis conceived of an experimental approach for obtaining standard potentials of the alkali metals. This approach involved using a solvent with which the alkali metals do not react. Ethylamine was the solvent chosen. In the following cell diagram, \(\mathrm{Na}(\text { amalg, } 0.206 \%)\) represents a solution of \(0.206 \%\) Na in liquid mercury. 1\. \(\mathrm{Na}(\mathrm{s}) | \mathrm{Na}^{+}(\text {in ethylamine }) | \mathrm{Na}(\text { amalg }, 0.206 \%)\) \(E_{\text {cell }}=0.8453 \mathrm{V}\) Although Na(s) reacts violently with water to produce \(\mathrm{H}_{2}(\mathrm{g}),\) at least for a short time, a sodium amalgam electrode does not react with water. This makes it possible to determine \(E_{\text {cell }}\) for the following voltaic cell. 2\. \(\mathrm{Na}(\text { amalg }, 0.206 \%)\left|\mathrm{Na}^{+}(1 \mathrm{M}) \| \mathrm{H}^{+}(1 \mathrm{M})\right|\) $$\mathrm{H}_{2}(\mathrm{g}, 1 \mathrm{atm}) \quad E_{\mathrm{cell}}=1.8673 \mathrm{V}$$ (a) Write equations for the cell reactions that occur in the voltaic cells (1) and (2) (b) Use equation (20.14) to establish \(\Delta G\) for the cell reactions written in part (a). (c) Write the overall equation obtained by combining the equations of part (a), and establish \(\Delta G^{\circ}\) for this overall reaction. (d) Use the \(\Delta G^{\circ}\) value from part (c) to obtain \(E_{\text {cell }}^{\circ}\) for the overall reaction. From this result, obtain \(E_{\mathrm{Na}^{+}}^{\circ} / \mathrm{Na}\) Compare your result with the value listed in Appendix D.

Consider the following electrochemical cell: $$ \operatorname{Pt}(\mathrm{s})\left|\mathrm{H}_{2}(\mathrm{g}, 1 \mathrm{atm})\right| \mathrm{H}^{+}(1 \mathrm{M}) \| \mathrm{Ag}^{+}(x \mathrm{M}) | \mathrm{Ag}(\mathrm{s}) $$ (a) What is \(E_{\text {cell }}^{\circ}-\) that is, the cell potential when \(\left[\mathrm{Ag}^{+}\right]=1 \mathrm{M} ?\) (b) Use the Nernst equation to write an equation for \(E_{\text {cell }}\) when \(\left[\mathrm{Ag}^{+}\right]=x\) (c) Now imagine titrating \(50.0 \mathrm{mL}\) of \(0.0100 \mathrm{M}\) \(\mathrm{AgNO}_{3}\) in the cathode half-cell compartment with 0.0100 M KI. The titration reaction is $$\mathrm{Ag}^{+}(\mathrm{aq})+\mathrm{I}^{-}(\mathrm{aq}) \longrightarrow \mathrm{AgI}(\mathrm{s})$$ Calculate \(\left[\mathrm{Ag}^{+}\right]\) and then \(E_{\text {cell }}\) after addition of the following volumes of \(0.0100 \mathrm{M} \mathrm{KI}:(\mathrm{i}) 0.0 \mathrm{mL} ;(\mathrm{ii}) 20.0 \mathrm{mL}\) (iii) \(49.0 \mathrm{mL} ;(\text { iv }) 50.0 \mathrm{mL} ;(\mathrm{v}) 51.0 \mathrm{mL} ;(\mathrm{vi}) 60.0 \mathrm{mL}\) (d) Use the results of part (c) to sketch the titration curve of \(E_{\text {cell }}\) versus volume of titrant.

Briefly describe each of the following ideas, methods, or devices: (a) salt bridge; (b) standard hydrogen electrode (SHE); (c) cathodic protection; (d) fuel cell.

The gas evolved at the anode when \(\mathrm{K}_{2} \mathrm{SO}_{4}(\mathrm{aq})\) is electrolyzed between Pt electrodes is most likely to be (a) \(\mathrm{O}_{2} ;\) (b) \(\mathrm{H}_{2} ;\) (c) \(\mathrm{SO}_{2} ;\) (d) \(\mathrm{SO}_{3} ;\) (e) a mixture of sulfur oxides.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free