IB Chemistry HL 100113

Reactivity 3.2: Electron transfer reactions

#Reactivity 3.2.1

Oxidation and reduction

Oxidation and reduction can be described in terms of electron transfer, change in oxidation state, oxygen gain/loss or hydrogen loss/gain.

Deduce oxidation states of an atom in a compound or an ion.

Identify the oxidized and reduced species and the oxidizing and reducing agents in a chemical reaction.

Include examples to illustrate the variable oxidation states of transition element ions and of most main group non-metals.

Include the use of oxidation numbers in the naming of compounds.

#Reactivity 3.2.2

Half-equations

Half-equations separate the processes of oxidation and reduction, showing the loss or gain of electrons.

Deduce redox half-equations and equations in acidic or neutral solutions.

#Reactivity 3.2.3

Relative ease of oxidation and reduction

The relative ease of oxidation and reduction of an element in a group can be predicted from its position in the periodic table.

The reactions between metals and aqueous metal ions demonstrate the relative ease of oxidation of different metals.

Predict the relative ease of oxidation of metals.

Predict the relative ease of reduction of halogens.

Interpret data regarding metal and metal ion reactions.

The relative reactivity of metals observed in metal/metal ion displacement reactions does not need to be learned; appropriate data will be supplied in examination questions.

#Reactivity 3.2.4

Acids + metals

Acids react with reactive metals to release hydrogen.

Deduce equations for reactions of reactive metals with dilute HCl and H2SO4.

#Reactivity 3.2.5

Electrochemical cells

Oxidation occurs at the anode and reduction occurs at the cathode in electrochemical cells.

Identify electrodes as anode and cathode, and identify their signs/polarities in voltaic cells and electrolytic cells, based on the type of reaction occurring at the electrode.

#Reactivity 3.2.6

Primary (voltaic) cells

A primary (voltaic) cell is an electrochemical cell that converts energy from spontaneous redox reactions to electrical energy.

Explain the direction of electron flow from anode to cathode in the external circuit, and ion movement across the salt bridge.

Construction of primary cells should include: half-cells containing metal/metal ion, anode, cathode, electric circuit, salt bridge.

#Reactivity 3.2.7

Secondary (rechargeable) cells

Secondary (rechargeable) cells involve redox reactions that can be reversed using electrical energy.

Deduce the reactions of the charging process from given electrode reactions for discharge, and vice versa.

Include discussion of advantages and disadvantages of fuel cells, primary cells and secondary cells.

#Reactivity 3.2.8

Electrolysis

An electrolytic cell is an electrochemical cell that converts electrical energy to chemical energy by bringing about non-spontaneous reactions.

Explain how current is conducted in an electrolytic cell.

Deduce the products of the electrolysis of a molten salt.

Construction of electrolytic cells should include: DC power source connected to anode and cathode, electrolyte.

#Reactivity 3.2.9

Oxidation in organic compounds

Functional groups in organic compounds may undergo oxidation.

Deduce equations to show changes in the functional groups during oxidation of primary and secondary alcohols, including the two-step reaction in the oxidation of primary alcohols.

Include explanation of the experimental set-up for distillation and reflux.

Include the fact that tertiary alcohols are not oxidized under similar conditions.

Names and formulas of specific oxidizing agents, and the mechanisms of oxidation, will not be assessed.

#Reactivity 3.2.10

Reduction in organic compounds

Functional groups in organic compounds may undergo reduction.

Deduce equations to show reduction of carboxylic acids to primary alcohols via the aldehyde, and reduction of ketones to secondary alcohols.

Include the role of hydride ions in the reduction reaction.

Names and formulas of specific reducing agents, and the mechanisms of reduction, will not be assessed.

#Reactivity 3.2.11

Reduction of unsaturated compounds

Reduction of unsaturated compounds by the addition of hydrogen lowers the degree of unsaturation.

Deduce the products of the reactions of hydrogen with alkenes and alkynes.

#Reactivity 3.2.12 (AHL)

Standard hydrogen electrode

The hydrogen half-cell H(aq)++e12H2(g)H^+_{(aq)} + e^- ⇌ \dfrac{1}{2} H_{2 (g)} is assigned a standard electrode potential of zero by convention. It is used in the measurement of standard electrode potential, EE^{⦵}.

Interpret standard electrode potential data in terms of ease of oxidation/reduction.

Standard reduction potentials are given in the data booklet.

#Reactivity 3.2.13 (AHL)

Standard cell potentials

Standard cell potential, EcellE^{⦵}_{\text{cell}}, can be calculated from standard electrode potentials. EcellE^{⦵}_{\text{cell}} has a positive value for a spontaneous reaction.

Predict whether a reaction is spontaneous in the forward or reverse direction from EE^{⦵} data.

#Reactivity 3.2.14 (AHL)

Gibbs energy and cell potentials

The equation ΔG=nFEcellΔG^{⦵} = - nFE^{⦵}_{\text{cell}} shows the relationship between standard change in Gibbs energy and standard cell potential for a reaction.

Determine the value for ΔGΔG^{⦵} from EE^{⦵} data.

The equation and the value of FF in C mol-1 are given in the data booklet.

#Reactivity 3.2.15 (AHL)

Electrolysis of aqueous solutions

During electrolysis of aqueous solutions, competing reactions can occur at the anode and cathode, including the oxidation and reduction of water.

Deduce from standard electrode potentials the products of the electrolysis of aqueous solutions.

Electrolytic processes should include the electrolysis of water and of aqueous solutions.

The effects of concentration and the nature of the electrode are limited to the electrolysis of NaCl(aq) and CuSO4(aq).

#Reactivity 3.2.16 (AHL)

Electroplating

Electroplating involves the electrolytic coating of an object with a metallic thin layer.

Deduce equations for the electrode reactions during electroplating.

Reactivity 3.1
Proton transfer reactions
Reactivity 3.3
Electron sharing reactions