2.3 - Predicting Redox Reactions in Solution
Module 5
Lesson 2.3 Predicting Redox Reactions in Solution
Key Concepts
Redox reactions can involve various substances that sometimes act in combination to promote the oxidation or reduction of other substances.
What if you were given a mixture of reactants and asked to predict the balanced redox reaction? Would you be able to do this?The following five-step method enables you to predict the most likely redox reaction that will occur in solution.
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List all entities initially present as they exist in an aqueous environment. Refer to Table 6 on page 575 of the textbook and classify each substance as an oxidizing agent, reducing agent, or both.
- Remember to dissociate soluble ionic compounds and list H2O(l) as one of your entities.
- Recall that some substances can act as both oxidizing agent (OA) and reducing agent (RA), such as H2O(l), Fe2+(aq), Sn2+(aq).
- Consider that some oxidizing and reducing agents occur in combination. For example, MnO4- only acts as an oxidizing agent in acidic conditions (MnO4-/H+). Unless you are advised specifically that acid is present, you cannot assume that H+ ions are present!
- Assume that any substances not present in the table are spectator ions and, therefore, can be ignored.
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From the list of potential oxidizing agents that you have generated, identify the strongest oxidizing agent and write its half-reaction from the redox table. Remember that oxidizing agents are listed on the left-hand side of the table with the strongest OA located at the top of the table.
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From the list of potential reducing agents that you have listed, identify the strongest reducing agent and write its half-reaction from the redox table. Remember that reducing agents are listed on the right-hand side of the table with the strongest RA located at the bottom of the table.
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Balance the number of electrons transferred by multiplying one or both half-reactions by a coefficient.
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Add the half-reactions to obtain a net ionic reaction and identify the reaction as spontaneous or non-spontaneous.
The following two examples illustrate how the above steps can be used to predict the most likely redox reaction occurring in solution.
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A strip of zinc is placed in a chromium(III) chloride solution.
Species List \( \mathrm { Zn(s),~Cr^{3+}(aq),~Cl^-(aq),~H_2O(l) } \) Oxidizing Agents \( \mathrm { Cr^{3+}(aq),~H_2O(l) } \)
\( \mathrm { SOA= Cr^{3+}(aq) } \)Reducing Agents \( \mathrm { Zn(s), ~Cl^-(aq),~H_2O(l),~Cl^-(aq)~and~H_2O(l) } \)
\( \mathrm { SRA= Zn(s) } \)Reduction Half-Reaction \( \mathrm { 2 (Cr^{3+}(aq)+ e^- \rightarrow Cr^{2+}(aq)) } \) Oxidation Half-Reaction \( \mathrm { Zn(s) \rightarrow Zn^{2+}(aq) + 2e^- } \) Net Ionic Equation \( \mathrm { 2 Cr^{3+}(aq) + Zn(s) \rightarrow 2 Cr^{2+}(aq) + Zn^{2+}(aq) } \) The reaction is spontaneous Empirical Evidence - Solid zinc disintegrates.
- Green colour of chromium(III) ions fades.
- Blue colour of chromium(II) ions appears.
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An acidified tin(II) bromide solution is mixed with a solution of potassium dichromate.
Species List \( \mathrm { Sn^{2+}(aq),~ Br^-(aq),~ H^+(aq),~ K^+(aq),~ Cr_2O_7^{2-}(aq),~ H_2O(l) } \) Oxidizing Agents \( \mathrm { Sn^{2+}(aq),~ H^+(aq),~ K^+(aq), Cr_2O_7^{2-}(aq)~ and~ H+(aq),~ H_2O(l) } \)
\( \mathrm { SOA= Cr_2O_7^{2-}(aq) ~ and~ H^+(aq) } \)Reducing Agents \( \mathrm { Sn^{2+}(aq),~ Br^-(aq),~ H_2O(l) } \)
\( \mathrm { SRA = Sn^{2+}(aq) } \)Reduction Half-Reaction \( \mathrm { Cr_2O_7^{2-}(aq) + 14 H^+(aq) + 6 e^- \rightarrow 2 Cr^{3+}(aq) + 7 H_2O(l) } \) Oxidation Half-Reaction \( \mathrm { 3 (Sn^{2+}(aq) \rightarrow Sn^{4+}(aq) + 2e^-) } \) Net Ionic Equation \( \mathrm { Cr_2O_7^{2-}(aq) + 14 H^+(aq) + 3 Sn^{2+}(aq) \rightarrow 3 Sn^{4+}(aq) + 2 Cr^{3+}(aq) + 7 H_2O(l) } \) The reaction is spontaneous. Empirical Evidence - pH increases as H+(aq) is consumed.
- Orange colour of dichromate ions fades.
- Green colour of chromium(III) ions appears.
Watch
Read from page 575 to the end of "Communication example 1" on page 577 of the textbook. A summary of the five-step method described in this section appears on page 578.
Check Your Understanding
Go to the textbook and Complete "Practice" Question 26 on page 579 and Section 13.2 Question 9 on page 582. Consult Table 1 on page 805 of the text for a list of some standard diagnostic tests.
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Species List \( \mathrm { Zn(s), ~H^+(aq), ~Cl^-(aq), ~H_2O(l) } \) Oxidizing Agents \( \mathrm { H^+(aq),~ H_2O(l) } \)
\( \mathrm { Strongest ~OA = H^+(aq) } \)Reducing Agents \( \mathrm { Zn(s),~ Cl^-(aq),~ H_2O(l),~ Cl^-(aq)~ and~ H_2O(l) } \)
\( \mathrm { Strongest ~RA = Zn(s) } \)Reduction Half-Reaction \( \mathrm { 2 H^+ (aq) + 2 e^- \rightarrow H_2(g) } \) Oxidation Half-Reaction \( \mathrm { Zn(s) \rightarrow Zn^{2+}(aq) + 2 e^- } \) Net Equation \( \mathrm { 2 H^+ (aq) + Zn(s) \rightarrow H_2(g) + Zn^{2+}(aq) } \) The reaction is spontaneous because the position of the SOA is above the SRA in the table. Diagnostic Tests To test for hydrogen, use a "pop" test. A "pop" sound is heard when a flame is inserted into the gas produced by the reaction.
Measure pH change before and after the reaction. pH is expected to increase as H+ are consumed.
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Species List \( \mathrm { Au(s),~ H^+(aq), ~Cl^-(aq),~ H_2O(l) } \) Oxidizing Agents \( \mathrm { H^+(aq),~ H_2O(l) } \)
\( \mathrm { Strongest~ OA = H^+(aq) } \)Reducing Agents \( \mathrm { Au(s),~ Cl^-(aq), ~H_2O(l),~ Cl^-(aq) ~and~ H_2O(l) } \)
\( \mathrm { Strongest~ RA = H_2O(l) } \)Reduction Half-Reaction \( \mathrm { 2(2 H^+ (aq) + 2 e^- \rightarrow H_2(g) ) } \) Oxidation Half-Reaction \( \mathrm { 2 H_2O(l) \rightarrow O_2(g) + 4 H^+(aq) + 4 e^- } \) Net Equation \( \mathrm { 2 H_2O(l) \rightarrow 2 H_2(g) + O_2(g) } \) The reaction is non-spontaneous because the position of the SOA is below the SRA in the table. Diagnostic Tests No change in observable properties
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Species List \( \mathrm { H^+(aq),~ NO_3^-(aq),~Cu(s), H_2O(l) } \) Oxidizing Agents \( \mathrm { H^+(aq),~ H^+(aq) ~and ~NO_3^-(aq),~ H_2O(l) } \)
\( \mathrm { Strongest~ OA = H^+(aq) ~and~ NO_3^-(aq) } \)Reducing Agents \( \mathrm { Cu(s),~ H_2O(l) } \)
\( \mathrm { Strongest~ RA = Cu(s) } \)Reduction Half-Reaction \( \mathrm { 2 NO_3^-(aq) + 4 H^+ (aq) + 2 e^- \rightarrow N_2O_4(g) + 2 H_2O(l) } \) Oxidation Half-Reaction \( \mathrm { Cu(s) \rightarrow Cu^{2+}(aq) + 2 e^- } \) Net Equation \( \mathrm { 2 NO_3^{-}(aq) + 4 H^+ (aq) + Cu(s) \rightarrow N_2O_4(g) + 2 H_2O(l) + Cu^{2+}(aq) } \) The reaction is spontaneous because the position of the SOA is above the SRA in the table. Diagnostic Tests Observe colour changes as the reaction proceeds. A blue colour is expected to develop as aqueous copper(II) ions are produced by the reaction. In addition, the solution containing the products of the reaction should produce a blue flame. Bubbles of gas should be evident. The pH should increase as H+(aq) ions are consumed.