standard reduction potential
/ E-naught /
Think of standard reduction potential as a score for how badly a species wants to grab electrons — its electron appetite, measured in volts. The bigger and more positive the number, the more eagerly the species pulls electrons toward itself and undergoes reduction. A strongly negative number means the opposite: this species would rather give electrons away, so it tends to be oxidized instead.
Precisely, the standard reduction potential E° is the voltage of a half-cell written as a reduction, measured against the standard hydrogen electrode (defined as 0 V), with every species at standard conditions: 1 molar for solutes, 1 bar for gases, pure solids and liquids, at a stated temperature (usually 298 K). For F2 + 2 e- -> 2 F- the value is a huge +2.87 V (fluorine is desperate for electrons), while for Li+ + e- -> Li it is -3.04 V (lithium clings hardest to its electron). To get a whole cell's potential you subtract: E°cell = E°cathode - E°anode, taking both values straight from the reduction table.
These numbers are the quantitative backbone of redox prediction. A positive E°cell means the reaction is spontaneous as written; potentials also link straight to thermodynamics through dG° = -nFE°. But two honest cautions: potential tells you only whether a reaction can go, never how fast (aluminium 'should' react with air far more than it does, saved by a kinetic oxide skin); and the tabulated values assume standard conditions and a particular pH — change the concentration or acidity and the real potential shifts, which is exactly what the Nernst equation handles.
For Zn | Zn2+ || Cu2+ | Cu: E°cell = E°(Cu2+/Cu) - E°(Zn2+/Zn) = (+0.34) - (-0.76) = +1.10 V. Positive, so the reaction is spontaneous.
Cathode minus anode; a positive cell potential means spontaneous.
E° measures thermodynamic tendency, not rate. A reaction with a hefty positive potential can still be vanishingly slow if no low-energy pathway exists — spontaneity is not the same as speed.