chem 30 redox

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Last updated 1:37 AM on 6/19/26
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55 Terms

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Oxidizing Agent (OA)

A substance that undergoes reduction and causes another substance to be oxidized, meaning its oxidation number decreases.

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Reducing Agent (RA)

A substance that undergoes oxidation and causes another substance to be reduced, meaning its oxidation number increases.

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Reduction

The gain of electrons by a chemical species, resulting in a decrease in its overall oxidation number.

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Oxidation

The loss of electrons by a chemical species, resulting in an increase in its overall oxidation number.

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Hydrogen Oxidation Number in Metallic Hydrides

It is exactly -1 in compounds like $NaH$, $CaH_2$, or $BaH_2$, serving as a major exception to the standard +1 rule.

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Dissociation Rule: Soluble Ionic Compounds

They completely dissociate into two separate ions in aqueous solution, identified by starting with a metal or the ammonium ion ($NH_4^+$).

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Dissociation Rule: Molecular Compounds

They consist entirely of non-metals and stay completely together as whole molecules instead of dissociating in solution.

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Dissociation Rule: Strong Acids

They fully split into two separate ions in solution, consisting of the 6 strong acids: $HClO_4$, $HI$, $HBr$, $HCl$, $H_2SO_4$, and $HNO_3$.

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Dissociation Rule: Weak Acids

They do not fully ionize or dissociate in solution and must be listed intact as a single molecular compound.

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Listing Species: "Acidic" Condition

You must explicitly list hydronium

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Listing Species: "Basic" Condition

You must explicitly list hydroxide ions ($OH^-_{(aq)}$) as a species present in the mixture.

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Listing Species: Aqueous Solutions

You must always list water ($H_2O_{(l)}$) as an available species since it serves as the solvent.

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Typical Oxidizing Agents (OAs)

Chemical species including metallic cations, acidic solutions, and halogens.

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Typical Reducing Agents (RAs)

Chemical species including neutral metals, basic solutions, and halide ions.

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Amphoteric Redox Species (Both OA and RA)

Chemical species that can act as either an oxidizing agent or a reducing agent, specifically $Cr^{2+}$, $Sn^{2+}$, $Fe^{2+}$, and $H_2O$.

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Empirical Evidence: Solid Reactant

The overall mass of the solid substance will decrease as it undergoes the reaction.

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Empirical Evidence: Solid Product

The overall mass of the solid substance will increase as it plates out or deposits.

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Empirical Evidence: Precipitate Formation

If you form a positive ion and a negative ion together on the product side, you must check the solubility table to watch for a precipitate.

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Empirical Evidence: $H^+_{(aq)}$ as a Reactant

The total concentration of $H^+$ will decrease, causing the reaction mixture to become less acidic and the pH to increase.

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Empirical Evidence: $H^+_{(aq)}$ as a Product

The total concentration of $H^+$ will increase, causing the reaction mixture to become more acidic and the pH to decrease.

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Empirical Evidence: $OH^-_{(aq)}$ as a Reactant

The total concentration of $OH^-$ will decrease, causing the reaction mixture to become less basic and the pH to decrease.

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Empirical Evidence: $OH^-_{(aq)}$ as a Product

The total concentration of $OH^-$ will increase, causing the reaction mixture to become more basic and the pH to increase.

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Empirical Evidence: Coloured Ion as a Reactant

The intensity of the color in the solution will lighten, fade, or completely disappear during the reaction.

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Empirical Evidence: Coloured Ion as a Product

The intensity of the color in the solution will darken, deepen, or brighten during the reaction.

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Empirical Evidence: Coloured Ion as Both Reactant and Product

The color of the solution will directly shift from the original reactant color to the newly formed product color.

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Titration Lab: Manipulated Variable

The exact volume of the sample being titrated, which functions as the independent variable.

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Titration Lab: Responding Variable

The total volume of titrant added to reach the endpoint, alongside the specific color change of the endpoint.

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Titration Lab: Controlled Variables

The concentration of the standard solution, the initial concentration of the unknown sample, and environmental parameters kept constant.

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Quality Check for Titration Trials

Good trials must have volumes within 0.2 mL of each other, measured as the difference between the largest and smallest accepted trial volumes.

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Voltaic Cell

An electrochemical cell that spontaneously converts chemical energy into electrical energy, acting as a functional battery with a positive net voltage.

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Electrolytic Cell

An electrochemical cell that uses an external power supply to non-spontaneously convert electrical energy into chemical energy, possessing a negative net voltage.

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Electrode

A solid piece of conducting material where half-reactions take place that must be able to conduct electricity.

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Cathode

The site of the reduction half-reaction in an electrochemical cell, always located in the half-cell containing the strongest oxidizing agent (SOA); attracts cations.

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Anode

The site of the oxidation half-reaction in an electrochemical cell, always located in the half-cell containing the strongest reducing agent (SRA); attracts anions.

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Direction of Electron Flow

Electrons always travel through the external wire from the anode to the cathode, moving from negative to positive in a voltaic cell.

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Salt Bridge

Porous Cup

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Direction of Anion Migration

Negative ions (anions) always move through the salt bridge or porous boundary directly towards the anode.

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Direction of Cation Migration

Positive ions (cations) always move through the salt bridge or porous boundary directly towards the cathode.

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Inert Electrode

A solid metal or carbon

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Standard Cell Notation Format

Electrode (s) | Electrolyte (aq) || Electrolyte (aq) | Electrode (s), where single lines denote phase boundaries and double lines denote a porous boundary or salt bridge.

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Cell Potential Formula ($\Delta E$)

$\Delta E = E_{r(\text{cathode})} - E_{r(\text{anode})}$ or $\Delta E = E_{r(\text{SOA})} - E_{r(\text{SRA})}$.

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Sign-Reversal Rule for Oxidation Potential

The oxidation potential of any given substance is exactly equal to its standard reduction potential with the mathematical sign reversed.

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Chloride Anomaly

When chloride ions ($Cl^-$) and water ($H_2O$) compete to act as the strongest reducing agent (SRA) in an electrolytic cell, chloride ions win out and oxidize instead of water.

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KI Electrolysis: Cathode Half-Reaction

$2H_2O_{(l)} + 2e^- \rightarrow H_{2(g)} + 2OH^-_{(aq)}$ with an standard reduction potential ($E^\circ_r$) of -0.83 V.

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KI Electrolysis: Anode Half-Reaction

$2I^-{(aq)} \rightarrow I{2(aq)} + 2e^-$ with an standard reduction potential ($E^\circ_r$) of +0.54 V.

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KI Electrolysis: Minimum Voltage Required

A total minimum applied voltage of +1.37 V is required, calculated from a net cell potential ($E^\circ_{\text{net}}$) of -1.37 V.

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Corrosion Prevention: Paint

A barrier method that prevents rust by shielding the metal from direct physical exposure to oxygen and moisture.

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Corrosion Prevention: Galvanizing

Coating a metal structure with a layer of zinc ($Zn_{(s)}$), which reacts with oxygen to build a protective $ZnO_{(s)}$ coating over the underlying metal.

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Corrosion Prevention: Sacrificial Anode

Deliberately installing a highly reactive metal (such as magnesium, $Mg$) to act as the SRA and corrode first, ensuring the protected metal is no longer the SRA.

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Corrosion Prevention: Impressed Current

Applying an external DC electrical power supply that continuously delivers electrons to environmental oxidizing agents so the valuable metal is not oxidized.

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Moles of Electrons Formula ($n_e$)

$n_e = \frac{It}{F}$, a critical equation that is not in your standard chemistry data booklet and must be completely memorized.

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Faraday's Law: Variable $I$

Represents the current measured in Amperes (A) or Coulombs per second (C

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Faraday's Law: Variable $t$

Represents the total elapsed time, which must always be mathematically converted into seconds (s).

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Faraday's Law: Variable $F$

Represents the Faraday constant, which possesses a standard value of $9.65 \times 10^4\text{ C

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Faraday's Law Formula Rearranged for Current ($I$)

$I = \frac{n_e F}{t}$.