MindMap Gallery Redox reaction and electrode potential (1)
This is a mind map about redox reactions and electrode potential (1), including the Nernst equation of electrode potential, the application of electromotive force and electrode potential, the thermodynamics of primary batteries, etc.
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Redox reactions and electrode potential
Redox reactions
Oxidation value
It is not necessarily consistent with the valence (the ratio of the number of atoms combined).
e.g. The C oxidation numbers of CH4 and CHCl3 are -4 and 2 respectively, but their valencies are all 4.
The apparent charge of an atom of an element
redox half reaction
Half reactions consist of different oxidation numbers of atoms of the same element, where oxygen The one with a higher chemical number is in the oxidation state, and the one with a lower oxidation number is in the reduced state.
Oxidation state (Ox) ne -→Reduction state (Red)
Redox couple: oxidized state/reduced state Ox/Red
When the medium or other substances in the solution participate in the half-reaction, it should also be written
Balancing redox reaction equations (ion-electron method)
write ionic equation
Write a half-reaction based on the redox couple
Balance half-reactions (especially O atoms) according to mass conservation and charge conservation
Determine the two half-reaction coefficients and combine the half-reactions
step
Primary battery
Galvanic cell reaction: two half reactions
Re1 Ox2 == Ox1 Re2
Battery composition
(-) Zn(s)︱ZnSO4(c1) ||CuSO4 (c2) ︱Cu(s) ( )
Electrode type
Metal - metal ion electrode
Gas-Ion Electrode
Metal - Metal refractory salt electrode
Redox electrode or concentration electrode
Generation of electrode potential
A "double electric layer" is formed between the metal surface and the solution interface. That is, the electrode potential difference
Standard electrode potential φθ
When the electrode to be measured is in the standard state, the electrode potential is measured, but the absolute value of the electrode potential cannot be measured.
Eθ=φθ( ) - φθ(-)
ΔGθ = -nFEθ
lnKθ = nFEθ/(RT)
application
Standard electrodes and commonly used electrodes
Standard hydrogen electrode: the electrode potential is set to 0
Calomel electrode: Hg2Cl2(s) 2e -== 2Hg(l) 2Cl -(aq), φ(Hg2Cl2/Hg)=0.2412 (saturated)
Silver chloride electrode: AgCl(s) e -==Ag(s) Cl-(aq), φ(AgCl/Ag)=0.2223 (1mol/L)
Thermodynamics of galvanic cells
The relationship between △rGm and E
△rGm=-nFE
Relationship between Kθ and Eθ
lnKθ = nFEθ/(RT) lgKθ = nEθ/0.05916 (when T=298.15K)
Application of electromotive force and electrode potential
The redox properties of substances can be compared based on the relative magnitude of the electrode potential algebraic values. The strength of
Determine the direction of redox reactions
ΔG < 0, E > 0, spontaneous (output useful work)
ΔG = 0, E = 0, equilibrium
ΔG > 0, E < 0 cannot proceed spontaneously
Measures the extent of redox reactions
Find the solubility product of poorly soluble salts
Nernst equation for electrode potential
acidity
Precipitation formation (important and difficult points)
Complex formation
Weak electrolyte generation
writing rules
The left is the negative electrode, which performs oxidation; the right is the positive electrode, which performs reduction.
“|” indicates the phase interface and there is a potential difference.
"||" means salt bridge. The solution is close to the salt bridge, which reduces the liquid junction potential to negligible
The temperature must be indicated, otherwise it means 298.15 K. The state of matter must be indicated, the pressure must be indicated for gases, and the concentration must be indicated for solutions.
Gas electrodes and redox electrodes should be written with conductive inert electrodes, usually platinum electrodes, written on the outside, with solids and gases close to the electrode plates.
Oxidation reaction ‖ Reduction reaction Low valence state │ High valence state ‖ High valence state │ Low valence state