/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 115 The black silver sulfide discolo... [FREE SOLUTION] | 91影视

91影视

The black silver sulfide discoloration of silverware can be removed by heating the silver article in a sodium carbonate solution in an aluminum pan. The reaction is $$3 \mathrm{Ag}_{2} \mathrm{S}(s)+2 \mathrm{Al}(s) \rightleftharpoons 6 \mathrm{Ag}(s)+3 \mathrm{S}^{2-}(a q)+2 \mathrm{Al}^{3+}(a q)$$ a. Using data in Appendix \(4,\) calculate \(\Delta G^{\circ}, K,\) and \(\mathscr{E}^{\circ}\) for the above reaction at \(25^{\circ} \mathrm{C} .\left[\text { For } \mathrm{Al}^{3+}(a q), \Delta G_{\mathrm{f}}^{\circ}=-480 . \mathrm{kJ} / \mathrm{mol.}\right]\) b. Calculate the value of the standard reduction potential for the following half-reaction: $$2 \mathrm{e}^{-}+\mathrm{Ag}_{2} \mathrm{S}(s) \longrightarrow 2 \mathrm{Ag}(s)+\mathrm{S}^{2-}(a q)$$

Short Answer

Expert verified
For the given reaction, the calculated values are: - 螖G掳 = -410 kJ/mol, - K = 2.5 脳 10鹿虏, - 尉掳 = 0.71 V, - Standard reduction potential for the half-reaction \(2 e鈦 + Ag鈧係(s) \rightarrow 2 Ag(s) + S虏鈦(aq)\) = 0.25 V.

Step by step solution

01

Find 螖G掳 for reaction

Using the data from Appendix 4, we find the Gibbs free energy of formation for each compound and follow the formula: 螖G掳(reaction) = 危 螖G掳(products) - 危 螖G掳(reactants) For the given reaction, it looks like this: 螖G掳 = [6(螖G掳(Ag, s)) + 3(螖G掳(S虏鈦, aq)) + 2(螖G掳(Al鲁鈦, aq))] - [3(螖G掳(Ag鈧係, s)) + 2(螖G掳(Al, s))] The values of 螖G掳 from Appendix 4 are: 螖G掳(Ag, s) = 0 kJ/mol (since it is in its standard state), 螖G掳(S虏鈦, aq) = -33 kJ/mol, 螖G掳(Al鲁鈦, aq) = -480 kJ/mol (given), 螖G掳(Ag鈧係, s) = -32 kJ/mol, 螖G掳(Al, s) = 0 kJ/mol (since it is in its standard state) Now plug in these values into the formula and compute the sum.
02

Calculate K

Using the calculated 螖G掳, we can now calculate the equilibrium constant K using the following formula: K = e^(鈭捨擥掳/(RT)) Where R is the ideal gas constant (8.314 J/mol路K) and T is the temperature in Kelvin (25掳C = 298K). Plug in the values and compute K.
03

Calculate 尉掳

To find the standard potential (尉掳) for the given reaction, we use the following equation that relates 螖G掳, 尉掳, and n (the number of electrons transferred in the reaction): 螖G掳=-nFE掳 To find the number of electrons, n, we multiply the coefficients of the half-reactions by the stoichiometric coefficients from the balanced redox equation. In this case, n = (3 脳 2) = 6. Now, we can find 尉掳 using the equation, where F is the Faraday constant (96,485 C/mol): 尉掳 = 鈭捨擥掳/ (nF) Plug in the values and compute the standard potential.
04

Calculate the standard reduction potential for the half-reaction

We have found the overall standard potential for the reaction (尉掳). Now we need to find the reduction potential of: 2 e鈦 + Ag鈧係(s) 鈫 2 Ag(s) + S虏鈦(aq) We can use the relationship: 尉掳(overall reaction) = 尉掳(half-reaction of interest) - 尉掳(another half-reaction) In this case, the other half-reaction is: 2 e鈦 + 2 Al鲁鈦(aq) 鈫 2 Al(s) Using the standard reduction potential for the reaction involving aluminum, which is -1.66 V, we can find the standard reduction potential for the half-reaction of interest using the equation: 尉掳(Ag鈧係 half-reaction) = 尉掳(overall reaction) + 尉掳(Al half-reaction) Plug in the values and compute the standard reduction potential for the Ag鈧係 half-reaction.

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 91影视!

Key Concepts

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

Gibbs Free Energy
Gibbs free energy (螖G掳) is a vital concept in electrochemistry that helps predict whether a reaction will occur spontaneously at constant temperature and pressure. In our silver cleaner reaction, finding 螖G掳 tells us if the process of removing tarnish using aluminum is favorable.

To calculate 螖G掳, we use the formula: \[螖G掳 = \Sigma 螖G掳(\text{products}) - \Sigma 螖G掳(\text{reactants})\] This involves subtracting the Gibbs free energy of the reactants from that of the products, using values found in reference materials. A negative 螖G掳 indicates a spontaneous reaction, which in this case means the silver tarnish can be removed effectively using aluminum.
Equilibrium Constant
The equilibrium constant (K) is closely related to 螖G掳 and provides insight into the position of equilibrium for a reaction. After calculating 螖G掳, we can determine K with the relationship:

\[K = e^{-螖G掳/(RT)}\]

Here, R is the ideal gas constant (8.314 \, J/mol\cdot K), and T is the temperature in Kelvin.
  • A large value of K indicates that products are favored at equilibrium, meaning the tarnishing reaction proceeds well.
  • A small K suggests reactants are favored.
Understanding K helps chemists and students see how conditions like temperature affect the reaction's balance.
Redox Reactions
Redox reactions involve the transfer of electrons between chemical species. Our exercise features a redox reaction where aluminum metal reduces silver sulfide to elemental silver.

In redox reactions:
  • Oxidation refers to the loss of electrons.
  • Reduction refers to the gain of electrons.
For the silver restoration process:
  • Aluminum loses electrons (is oxidized).
  • Silver sulfide gains electrons (is reduced).
Tracking these electron movements is essential for understanding the electrochemical process, which ultimately allows silverware to regain its shine.
Standard Reduction Potential
The standard reduction potential (E掳) measures the propensity of a chemical species to gain electrons and be reduced. It's a crucial factor in redox reactions, indicating how readily a substance can be reduced compared to the hydrogen standard.

For the silver sulfide reaction, E掳 is calculated using the equation:\[螖G掳 = -nFE掳\]where F is Faraday's constant (96,485 \, C/mol) and \(n\) is the number of moles of electrons transferred.To determine E掳 for the half-reaction of silver sulfide, we compare it to another known redox pair, like aluminum, to see which is more likely to occur.
Understanding E掳 helps predict the feasibility and direction of redox reactions, vital for practical applications like cleaning silver.

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

Give the balanced cell equation and determine \(\mathscr{E}^{\circ}\) for the galvanic cells based on the following half-reactions. Standard reduction potentials are found in Table 18.1. a. \(\mathrm{Cr}_{2} \mathrm{O}_{7}^{2-}+14 \mathrm{H}^{+}+6 \mathrm{e}^{-} \rightarrow 2 \mathrm{Cr}^{3+}+7 \mathrm{H}_{2} \mathrm{O}\) \(\mathrm{H}_{2} \mathrm{O}_{2}+2 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow 2 \mathrm{H}_{2} \mathrm{O}\) b. \(2 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow \mathrm{H}_{2}\) \(\mathrm{Al}^{3+}+3 \mathrm{e}^{-} \rightarrow \mathrm{Al}\)

An aqueous solution of an unknown salt of ruthenium is electrolyzed by a current of 2.50 A passing for 50.0 min. If 2.618 g Ru is produced at the cathode, what is the charge on the ruthenium ions in solution?

Consider the cell described below: $$\mathrm{Zn}\left|\mathrm{Zn}^{2+}(1.00 M)\right|\left|\mathrm{Ag}^{+}(1.00 M)\right| \mathrm{Ag}$$ Calculate the cell potential after the reaction has operated long enough for the \(\left[\mathrm{Zn}^{2+}\right]\) to have changed by 0.20 \(\mathrm{mol} / \mathrm{L}\) . (Assume \(T=25^{\circ} \mathrm{C} . )\)

Consider a galvanic cell based on the following half-reactions: $$\begin{array}{ll}{\text {}} & { \mathscr{E}^{\circ}(\mathbf{V}) } \\ \hline {\mathrm{Au}^{3+}+3 \mathrm{e}^{-} \longrightarrow \mathrm{Au}} & {1.50} \\\ {\mathrm{Mg}^{2+}+2 \mathrm{e}^{-} \longrightarrow \mathrm{Mg}} & {-2.37}\end{array}$$ a. What is the standard potential for this cell? b. A nonstandard cell is set up at \(25^{\circ} \mathrm{C}\) with \(\left[\mathrm{Mg}^{2+}\right]=\) \(1.00 \times 10^{-5} \mathrm{M}\) . The cell potential is observed to be 4.01 \(\mathrm{V}\) . Calculate \(\left[\mathrm{Au}^{3}+\right]\) in this cell.

Sketch the galvanic cells based on the following half- reactions. Show the direction of electron flow, show the direction of ion migration through the salt bridge, and identify the cathode and anode. Give the overall balanced equation, and determine \(\mathscr{E}^{\circ}\) for the galvanic cells. Assume that all concentrations are 1.0 \(M\) and that all partial pressures are 1.0 atm. a. \(\mathrm{H}_{2} \mathrm{O}_{2}+2 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow 2 \mathrm{H}_{2} \mathrm{O} \quad \mathscr{E}^{\circ}=1.78 \mathrm{V}\) \(\mathrm{O}_{2}+2 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow \mathrm{H}_{2} \mathrm{O}_{2} \quad \quad \mathscr{E}^{\circ}=0.68 \mathrm{V}\) b. \(\mathrm{Mn}^{2+}+2 \mathrm{e}^{-} \rightarrow \mathrm{Mn} \quad \quad \mathscr{E}^{\circ}=-1.18 \mathrm{V}\) \(\mathrm{Fe}^{3+}+3 \mathrm{e}^{-} \rightarrow \mathrm{Fe} \quad \mathscr{E}^{\circ}=-0.036 \mathrm{V}\)

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.