Redox reactions basic solutions

Balance the following redox reactions, and calculate the standard-state potential and the equilibrium constant for each. Assume that the [H3O+] is 1 M for acidic solutions, and that the [OH ] is 1 M for basic solutions. 

C19-0050. What are the half-reactions for these redox processes (a) Aqueous hydrogen peroxide acts on Co, and the products are hydroxide and Co , in basic solution, (b) Methane reacts with oxygen gas and produces water and carbon dioxide, (c) To recharge a lead storage battery, lead(II) sulfate is converted to lead metal and to lead(IV) oxide, (d) Zinc metal dissolves in aqueous hydrochloric acid to give ions and hydrogen gas. 

In electrocatalysis, the major subject are redox reactions occurring on inert, nonconsumable electrodes and involving substances dissolved in the electrolyte while there is no stoichiometric involvement of the electrode material. Electrocatalytic processes and phenomena are basically studied in aqueous solutions at temperatures not exceeding 120 to 150°C. Yet electrocatalytic problems sometimes emerge as well in high-temperature systems at interfaces with solid or molten electrolytes. 

In strongly basic solution this reaction involves the formation of an hydroxo bridge in addition to the dioxygen bridge 43). The redox potential for the process... 

In the practice of potentiometric titration there are two aspects to be dealt with first the shape of the titration curve, i.e., its qualitative aspect, and second the titration end-point, i.e., its quantitative aspect. In relation to these aspects, an answer should also be given to the questions of analogy and/or mutual differences between the potentiometric curves of the acid-base, precipitation, complex-formation and redox reactions during titration. Excellent guidance is given by the Nernst equation, while the acid-base titration may serve as a basic model. Further, for convenience we start from the following fairly approximate assumptions (1) as titrations usually take place in dilute (0.1 M) solutions we use ion concentrations in the Nernst equation, etc., instead of ion activities and (2) during titration the volume of the reaction solution is considered to remain constant. 

A solution of the isolated platinum blue compound usually contains several chemical species described in the previous section. Such complicated behaviors had long been unexplored, but were gradually unveiled as a result of the detailed equilibrium and kinetic studies in recent years. The basic reactions can be classified into four categories (l)HH-HT isomerization (2) redox disproportionation reactions (3) ligand substitution reactions, especially at the axial coordination sites of both Pt(3.0+)2 and Pt(2.5+)4 and (4) redox reactions with coexisting solvents and atmosphere, such as water and 02. In this chapter, reactions 1-4 are summarized. 

Perhaps the most important application of redox chemicals in the modern laboratory is in oxidation or reduction reactions that are required as part of a preparation scheme. Such preoxidation or prereduction is also frequently required for certain instrumental procedures for which a specific oxidation state is essential in order to measure whatever property is measured by the instrument. An example in this textbook can be found in Experiment 19 (the hydroxylamine hydrochloride keeps the iron in the +2 state). Also in wastewater treatment plants, it is important to measure dissolved oxygen (DO). In this procedure, Mn(OH)2 reacts with the oxygen in basic solution to form Mn(OH)3. When acidified and in the presence of KI, iodine is liberated and titrated. This method is called the Winkler method. 

Redox reactions do not always take place under neutral conditions. Balancing half-reactions is more complicated for reactions that take place in acidic or basic solutions. When an acid or base is present, or OH ions must also be considered. However, the overall approach is similar. This approach involves writing the correct formulas for the reactants and products, balancing the atoms, and adding the appropriate number of electrons to one side of the half-reaction to balance the charges. 

Balancing Redox Reactions in Acidic and Basic Solutions... 

The following redox reactions occur in basic solution. Balance the equations using the oxidation number method. 

Fig. 8-43. Anodic and cathodic polarization curves observed for a redox electron transfer at metallic tin electrodes covered with an anodic oxide Sn02 film of various thicknesses d in a basic solution reaction is a redox electron transfer of 0.25 M Fe(CN)6 A).25 M Fe(CN)6 in 0.2 M borate buffer solution of pH 9.1 at 25°C. d = film thickness dj = 2 nm ...

In basic solution, the redox potential for the half reaction, Mn04 - - 2H2O -1-3e —> Mn02 - - 40H-, is -1- 0.60V. 

The ion formation may occur in the bulk solution before the electrospray process takes place or in the gas phase by protonation or salt adduct formation, or by an electrochemical redox reaction. Polar compounds already exist in solution as ions therefore, the task of the electrospray is to separate them from their counterions. This is the case of many inorganic and organic species and all those compounds that show acidic or basic properties. Proteins, peptides, nucleotides, and many other bio- and pharmaceutical analytes are typical examples of substances that can be detected as proto-nated or deprotonated species. 

Alternatively, the fast autoxidation of mercaptans is achieved by working in basic solution and in the presence of transition metal catalysts, via reactions involving RS" anions and redox steps, much as for phenols (22). 

Consequently, reduction of cobalt(III) ammines in basic solution is not favorable. A variety of reducing agents has been used to effect reaction (11). The fortunate coincidences that cobalt(III) complexes are substitution inert while cobalt(II) systems are labile and that cobalt(II) is resistant to oxidation or further reduction in acid solution offer many advantages in the study of redox processes. Not surprisingly, work with cobalt(III) complexes forms the basis for much of the present understanding of oxidation-reduction reactions. 

This chapter deals with the fundamental aspects of redox reactions in non-aque-ous solutions. In Section 4.1, we discuss solvent effects on the potentials of various types of redox couples and on reaction mechanisms. Solvent effects on redox potentials are important in connection with the electrochemical studies of such basic problems as ion solvation and electronic properties of chemical species. We then consider solvent effects on reaction kinetics, paying attention to the role of dynamical solvent properties in electron transfer processes. In Section 4.2, we deal with the potential windows in various solvents, in order to show the advantages of non-aqueous solvents as media for redox reactions. In Section 4.3, we describe some examples of practical redox titrations in non-aqueous solvents. Because many of the redox reactions are realized as electrode reactions, the subjects covered in this chapter will also appear in Part II in connection with electrochemical measurements. 

To balance a redox reaction which occurs in a basic solution is a very similar to balancing a redox reaction which occurs in acidic conditions. First, balance the reaction as you would for an acidic solution and then adjust for the basic solution. Here is an example using the half-reaction method ... 

Redox reactions can be balanced in basic solutions as well. This task will require an additional step but it can still be done following the steps shown above. To balance the redox reaction H202 + C1031 — C1021- + 02 in a basic solution, do as follows ... 

Balancing oxidation-reduction reactions depends on whether the solution is acidic or basic. The method for balancing redox reactions in an acidic solution is as follows ... 

The method for balancing redox reactions in a basic solution is as follows ... 

So what are acids and bases Vinegar is actually a dilute solution of acetic acid in water, about a 5 percent solution, but it rather nicely displays the characteristic properties of acids they are sour, they turn purple-cabbage indicator red or pink, and they react with bases to form water. A solution of sodium bicarbonate nicely displays several of the characteristics of basic solutions it tastes bitter, it turns purple-cabbage indicator blue, and it reacts with acids to form water. The last property, listed for both acid and base, the ability to react with each other, is really the defining property because acid-base reactions, like redox reactions, occur in tandem one substance acts as an acid and one substance acts as a base. Acid neutralizes base and base neutralizes acid. 

---