3: Oxidation and Reduction of Elements
- Page ID
- 553788
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\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)- 3.1: Redox Reactions
- Chemical reactions in which electrons are transferred are called oxidation-reduction, or redox, reactions. Oxidation is the loss of electrons. Reduction is the gain of electrons. Oxidation and reduction always occur together, even though they can be written as separate chemical equations.
- 3.2: Balancing Redox Reactions
- In studying redox chemistry, it is important to begin by learning to balance electrochemical reactions. Simple redox reactions can be balanced by inspection, but for more complex reactions it is helpful to have a foolproof, systematic method. The ion-electron method allows one to balance redox reactions regardless of their complexity. We illustrate this method with two examples.
- 3.3: Electrochemical Cells
- Electrochemical cells typically consist of two half-cells. The half-cells separate the oxidation half-reaction from the reduction half-reaction and make it possible for current to flow through an external wire. One half-cell contains the anode. Oxidation occurs at the anode. The anode is connected to the cathode in the other half-cell. Reduction occurs at the cathode. Adding a salt bridge completes the circuit allowing current to flow.
- 3.4: Standard Reduction Potentials
- Assigning the potential of the standard hydrogen electrode (SHE) as zero volts allows the determination of standard reduction potentials, E°, for half-reactions in electrochemical cells. As the name implies, standard reduction potentials use standard states (1 bar or 1 atm for gases; 1 M for solutes, often at 298.15 K) and are written as reductions (where electrons appear on the left side of the equation).
- 3.5: Thermodynamic Considerations
- Electrical work is the negative of the product of the total charge (Q) and the cell potential (Ecell). The total charge can be calculated as the number of moles of electrons (n) times the Faraday constant (F = 96,485 C/mol e−). Electrical work is the maximum work that the system can produce and so is equal to the change in free energy. Thus, anything that can be done with or to a free energy change can also be done to or with a cell potential.
- 3.6: General Trends in Reactivity
- The redox properties of the elements very roughly follow the following general trends: Elements on the left of the periodic table tend to act as reductants; those on the right as oxidants The noble gases are inert and as elements tend not to act as good oxidants or reductants As one moves towards the left of the periodic table, elements tend to act as good reductants, while those towards the right tend to act as increasingly good oxidants. As one moves down a group of the periodic table, elemen
- 3.7: Latimer Diagrams
- Latimer diagrams helpfully summarize elements' redox chemistry in a compact format, showing only the redox-active species and the associated redox potentials. In a Latimer diagram, the product of each reduction half reaction is the reactant in the succeeding reduction half reaction, and the associated reduction potential is written above the reaction arrow. Because of this it is possible to represent the entire sequence of redox reactions even more compactly by writing out the reactions on a sin
- 3.8: Frost Diagrams
- Frost diagrams represent how stable an elements' redox states are relative to the free element. In a Frost diagram a proxy for the free energy relative to that of the free element (oxidation state zero) is plotted as a function of oxidation state.
- 3.9: Pourbaix Diagrams
- Pourbaix Diagrams plot electrochemical stability for different redox states of an element as a function of pH. As noted above, these diagrams are essentially phase diagrams that plot the map the conditions of potential and pH (most typically in aqueous solutions) where different redox species are stable. Typically, the water redox reactions are plotted as dotted lines on these more complicated diagrams for other elements.
- 3.10: Corrosion
- Corrosion is the degradation of a metal caused by an electrochemical process. Large sums of money are spent each year repairing the effects of, or preventing, corrosion. Some metals, such as aluminum and copper, produce a protective layer when they corrode in air. The thin layer that forms on the surface of the metal prevents oxygen from coming into contact with more of the metal atoms and thus “protects” the remaining metal from further corrosion. Iron corrodes (forms rust) when exposed to wate