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Topic R3.2 · SL and HL

Electron transfer reactions: notes and practice questions

Summary
  • This topic covers electron transfer reactions, including oxidation, reduction, and electrochemical cells.
  • Oxidation is electron loss, an increase in oxidation state, or oxygen gain/hydrogen loss.
  • Reduction is electron gain, a decrease in oxidation state, or oxygen loss/hydrogen gain.
  • Deduce oxidation states of atoms in compounds or ions.
  • Identify oxidized and reduced species, and oxidizing and reducing agents.
  • Half-equations show electron loss (oxidation) or gain (reduction).
  • Electrochemical cells involve oxidation at the anode and reduction at the cathode.
  • Voltaic cells convert spontaneous redox energy to electrical energy.
  • Electrolytic cells use electrical energy for non-spontaneous reactions, such as molten salt electrolysis.
  • Organic functional groups like alcohols, carboxylic acids, ketones, alkenes, and alkynes can undergo oxidation or reduction.

How it is examined

Oxidation state deduction is a 1-mark part in both papers. Balancing half-equations is 1 to 2 marks and the balance must be right in both atoms and charge. Voltaic cell diagrams attract "identify the anode", "state the direction of electron flow" and "explain the role of the salt bridge" at 1 mark each, and the salt bridge answer must mention ion movement to maintain electrical neutrality, not just "completes the circuit". At HL, E⦵cell calculations are [2] and the sign error from reversing the wrong half-cell is the classic loss. The organic oxidation sequence (primary alcohol to aldehyde with distillation, to carboxylic acid with reflux) is examined by asking for conditions as well as products.

Given in the booklet

HL: standard reduction potentials, the Faraday constant F, and ΔG⦵ = −nFE⦵cell. At SL nothing is given, but the guidance says displacement data will be supplied in the question. What is recall: oxidation state rules, anode is oxidation and cathode is reduction, the sign convention (anode negative in a voltaic cell, positive in an electrolytic cell), and the oxidation products of primary versus secondary versus tertiary alcohols.

Key ideas
  • 3.2.1 Oxidation and reduction can be described in terms of electron transfer, change in oxidation state, oxygen gain or loss, or hydrogen loss or gain. Students deduce oxidation states of an atom in a compound or an ion, and identify the oxidized and reduced species and the oxidizing and reducing agents in a chemical reaction.
  • 3.2.2 Half-equations separate the processes of oxidation and reduction, showing the loss or gain of electrons. Students deduce redox half-equations and equations in acidic or neutral solutions.
  • 3.2.3 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. Students predict the relative ease of oxidation of metals and of reduction of halogens, and interpret data regarding metal and metal ion reactions.
  • 3.2.4 Acids react with reactive metals to release hydrogen. Students deduce equations for reactions of reactive metals with dilute HCl and H₂SO₄.
Not assessed
  • Half-equations and equations are required in acidic or neutral solutions only. Balancing in alkaline solution is not on the syllabus.
  • Names and formulas of specific oxidizing agents, and the mechanisms of oxidation, will not be assessed. The same for reducing agents and the mechanisms of reduction. Include the role of hydride ions in the reduction reaction.
At HL
  • 3.2.12 The hydrogen half-cell `H⁺(aq) + e⁻ ⇌ ½H₂(g)` is assigned a standard electrode potential of zero by convention. It is used in the measurement of standard electrode potential, E⦵. Students interpret standard electrode potential data in terms of ease of oxidation and reduction.
  • 3.2.13 Standard cell potential, E⦵cell, can be calculated from standard electrode potentials. E⦵cell has a positive value for a spontaneous reaction. Students predict whether a reaction is spontaneous in the forward or reverse direction from E⦵ data.
  • 3.2.14 The equation `ΔG⦵ = −nFE⦵cell` shows the relationship between standard change in Gibbs energy and standard cell potential for a reaction. Students determine ΔG⦵ from E⦵ data.
  • 3.2.15 During electrolysis of aqueous solutions, competing reactions can occur at the anode and cathode, including the oxidation and reduction of water. Students deduce from standard electrode potentials the products of the electrolysis of aqueous solutions.

Guiding questions

  • What happens when electrons are transferred?

Linking questions

  • Structure 3.1 What are the advantages and limitations of using oxidation states to track redox changes? Why does metal reactivity increase, and non-metal reactivity decrease, down the main groups? How can oxidation states be used to show that CH₄, CH₃OH, HCHO, HCOOH, CO₂ are given in increasing order of oxidation?
  • Structure 2.3 The surface oxidation of metals is often known as corrosion. What are some of the consequences of this process?
  • Structure 2.1 Under what conditions can ionic compounds act as electrolytes?
  • Structure 3.2 How does the nature of the functional group in a molecule affect its physical properties, such as boiling point?
  • Reactivity 1.3 Electrical energy can be derived from the combustion of fossil fuels or from electrochemical reactions. What are the similarities and differences? What is the difference between combustion and oxidation of an alcohol?
  • Reactivity 2.3 Secondary cells rely on electrode reactions that are reversible. What are the common features of these reactions?
  • Reactivity 3.4 Why are some reactions of alkenes classified as reduction reactions while others are classified as electrophilic addition reactions?
  • Reactivity 1.4 (HL) How can thermodynamic data also be used to predict the spontaneity of a reaction?
  • Structure 3.1 (HL) Why is there a colour change when an alcohol is oxidized by a transition element compound?
  • Tool 1, Inquiry 2 Why are some redox titrations described as "self-indicating"? How is an electrolytic cell used for electroplating?

Practice questions

51 questions · 23 easy · 24 medium · 4 hard
Showing 20 of 20

Question 1

EasyPaper 2 · calculator1 mark

Sulfur is a versatile element, forming compounds with a wide range of oxidation states. In which of the following substances does sulfur exhibit the lowest oxidation number?

A H2SH_2S

B SO2SO_2

C SO32−SO_3^{2-}

D S8S_8

Question 2

MediumPaper 2 · calculator1 mark

A brass key is to be electroplated with copper. Which of the following statements are correct?

I The brass key should be the cathode.

II The anode is made of an inert material like graphite.

III The electrolyte could be aqueous copper(II) sulfate.

A. I only

B. II only

C. I and III only

D. I, II and III

Question 3

HardPaper 1B · calculator16 marks
(a)

Nitrogen dioxide, a pollutant from car exhausts, reacts with water in the atmosphere to form nitric acid and nitrous acid. This is a disproportionation reaction.

2NO2(g)+H2O(l)⇌HNO3(aq)+HNO2(aq)2NO_{2}(g) + H_{2}O(l) \rightleftharpoons HNO_{3}(aq) + HNO_{2}(aq)

(a) Deduce the oxidation states of nitrogen in the reactant and products.

Reactant: NO2NO_{2}

Products: HNO3HNO_{3}, HNO2HNO_{2}

[2]
(b)

(b) Explain, with reference to the equilibrium, why more nitrogen dioxide gas dissolves when the reaction occurs in alkaline rainwater.

[1]
(c)(i)

(c) The solubility of nitrogen dioxide gas in water was measured by different scientific groups. A summary of their results is shown.

SourceTemperature / °CSolubility of NO2NO_{2} gas in 0.100 dm³ of water
A00.380 dm³
B100.28 dm³
C20200 cm³
D250.15 L
E300.120 dm³

(i) Identify a problem in comparing the data from the different sources as presented in the table.

[1]
(c)(ii)

(ii) The units of solubility are converted to mol dm⁻³. Complete the table by calculating the value for source A. Assume the atmospheric pressure is 100 kPa and the density of the resulting solution is 1.00 g cm⁻³.

[2]
(c)(iii)

(iii) Suggest an explanation for the effect of temperature on the solubility of nitrogen dioxide gas.

[1]
(d)

(d) Suggest one reason why nitrogen dioxide is considered a major air pollutant.

[1]
(e)(i)

(e) Nitrous acid, HNO2HNO_2, is a weak acid. The graph shows the percentage of nitrous acid and its conjugate base, the nitrite ion (NO2−NO_2^-), present at different pH values.

(GRAPH IS A STANDARD SPECIATION PLOT FOR A WEAK ACID. X-AXIS: pH from 0 to 8. Y-AXIS: Percentage from 0 to 100. A curve for HA starts at 100% and goes down, a curve for A- starts at 0% and goes up. The two curves cross at pH = 3.3, where each is at 50%.)

(i) Deduce the pH range where nitrous acid, HNO2HNO_{2}, is the dominant nitrogen-containing species in the solution.

[1]
(e)(ii)

(ii) Determine, with reference to the graph, the pKapK_a of nitrous acid.

[2]
(f)(i)

(f) Nitrous acid can react with secondary amines to form N-nitrosamines, which are potent carcinogens. An example is the reaction with dimethylamine, (CH3)2NH(CH_3)_2NH.

(i) Deduce a balanced chemical equation for the formation of N-nitrosodimethylamine, (CH3)2NNO(CH_3)_2NNO, from dimethylamine and nitrous acid.

[1]
(f)(ii)

(ii) The rate of N-nitrosamine formation is highly dependent on pH. The reaction rate is highest under mildly acidic conditions where there is a sufficient concentration of both the unprotonated amine and nitrous acid. State two conditions that could be maintained in an industrial process to minimize the formation of N-nitrosamines.

[2]
(g)

(g) To combat the effects of acid rain, powdered limestone (CaCO3CaCO_3) is sometimes added to lakes. Suggest two distinct reasons why this 'liming' process is effective at restoring the aquatic ecosystem.

[2]

Question 4

EasyPaper 1A · calculator1 mark

Hydrogen sulfide, H2SH_2S, and the sulfate ion, SO42−SO_4^{2-}, are common species containing sulfur.

What are the oxidation states of sulfur in these species?

H2SH_2S

SO42−SO_4^{2-}

A. +2, +8

B. -2, +6

C. -2, +8

D. +2, +6

Question 5

MediumPaper 2 · calculator1 mark

When a student performs a redox titration, iron(II) ions react with permanganate ions in an acidic solution. The unbalanced equation for this reaction is given below:

Fe2+(aq)+MnO4−(aq)+H+(aq)→Fe3+(aq)+Mn2+(aq)+H2O(l)Fe^{2+}(aq) + MnO_4^-(aq) + H^+(aq) \rightarrow Fe^{3+}(aq) + Mn^{2+}(aq) + H_2O(l)

When the following redox equation is balanced using the smallest possible whole numbers, what is the sum of all the coefficients?

A 20

B 22

C 24

D 26

Question 6

HardPaper 2 · calculator24 marks
(a)(i)

Antimony (Sb) and Bismuth (Bi) are elements in group 15 of the periodic table.

(a) Antimony has two stable isotopes. 57.21% of antimony atoms contain 70 neutrons and the remainder contain 72 neutrons.

(i) Deduce the nuclear symbol of the isotope of antimony containing 72 neutrons. Use section 6 of the data booklet.

[1]
(a)(ii)

(ii) Calculate, to two decimal places, the relative atomic mass of antimony.

[2]
(b)(i)

Bismuth(III) nitrate, Bi(NO3)3Bi(NO_3)_3, is a common salt of bismuth.

(b) (i) The compound contains both ionic and covalent bonds. State which particles are joined by covalent bonds and which are joined by ionic bonds.

[2]
(b)(ii)

(ii) Distinguish between covalent and ionic bonding in terms of electron distribution.

[2]
(b)(iii)

(iii) State the enthalpy term that characterizes the strength of the bonding between the ions in an ionic solid.

[1]
(b)(iv)

(iv) Write an equation for the formation of aqueous bismuth(III) nitrate from solid bismuth(III) oxide and nitric acid.

[2]
(b)(v)

(v) Calculate the volume, in cm3cm^3, of 1.50 mol dm−31.50 \text{ mol dm}^{-3} nitric acid required to react completely with 5.00 g5.00 \text{ g} of solid bismuth(III) oxide.

[3]
(b)(vi)

(vi) Predict, with a reason, whether bismuth(III) oxide is expected to be primarily acidic, basic or amphoteric.

[1]
(b)(vii)

(vii) Discuss how the relative reactivity of zinc and bismuth could be established using the metals and aqueous solutions of their nitrates.

[2]
(b)(viii)

(viii) Discuss the products formed at the electrodes during the electrolysis of aqueous bismuth(III) nitrate. Use the standard electrode potential E⊖(Bi3+/Bi)=+0.32 VE^\ominus(Bi^{3+}/Bi) = +0.32 \text{ V} and section 24 of the data booklet.

[2]
(c)(i)

Bismuth compounds are sometimes used in fireworks to produce special effects.

(c) (i) State the feature of the atomic emission spectrum of an element that corresponds to its first ionization energy.

[1]
(c)(ii)

(ii) Calculate the wavelength, in nm, that corresponds to the first ionization energy of bismuth. Use sections 1, 2 and 8 of the data booklet.

[3]
(c)(iii)

(iii) Explain why the first ionization energy of bismuth is lower than that of polonium (Po), in terms of nuclear charge and electron shielding.

[2]

Question 7

EasyPaper 2 · calculator1 mark

In the electrolysis of molten sodium chloride, NaCl(l)NaCl(l), using inert electrodes, which of the following statements is correct?

A. Sodium metal is formed at the positive electrode (anode).
B. Chlorine gas is formed at the negative electrode (cathode).
C. For every mole of sodium metal produced, two moles of chlorine gas are produced.
D. For every mole of chlorine gas produced, two moles of sodium metal are produced.

Question 8

MediumPaper 2 · calculator1 mark

Use the following table of standard reduction potentials to answer the question.

Half-reactionE⊖/VE^\ominus / \text{V}
Na+(aq)+e−⇌Na(s)Na^+(aq) + e^- \rightleftharpoons Na(s)-2.71
Zn2+(aq)+2e−⇌Zn(s)Zn^{2+}(aq) + 2e^- \rightleftharpoons Zn(s)-0.76
Cr3+(aq)+3e−⇌Cr(s)Cr^{3+}(aq) + 3e^- \rightleftharpoons Cr(s)-0.74
Fe2+(aq)+2e−⇌Fe(s)Fe^{2+}(aq) + 2e^- \rightleftharpoons Fe(s)-0.45
2H+(aq)+2e−⇌H2(g)2H^+(aq) + 2e^- \rightleftharpoons H_2(g)0.00
Cu2+(aq)+2e−⇌Cu(s)Cu^{2+}(aq) + 2e^- \rightleftharpoons Cu(s)+0.34
Cu+(aq)+e−⇌Cu(s)Cu^+(aq) + e^- \rightleftharpoons Cu(s)+0.52
I2(aq)+2e−⇌2I−(aq)I_2(aq) + 2e^- \rightleftharpoons 2I^-(aq)+0.54
Fe3+(aq)+e−⇌Fe2+(aq)Fe^{3+}(aq) + e^- \rightleftharpoons Fe^{2+}(aq)+0.77
Ag+(aq)+e−⇌Ag(s)Ag^+(aq) + e^- \rightleftharpoons Ag(s)+0.80
Cl2(aq)+2e−⇌2Cl−(aq)Cl_2(aq) + 2e^- \rightleftharpoons 2Cl^-(aq)+1.36

A voltaic cell is constructed using the following half-cells: Cr(s)∣Cr3+(aq)∣∣Ag+(aq)∣Ag(s)Cr(s)|Cr^{3+}(aq)||Ag^{+}(aq)|Ag(s).

Which statement about this cell is correct?

A. The mass of the silver electrode decreases.

B. The chromium electrode is the cathode.

C. Electrons flow from the silver electrode to the chromium electrode.

D. The concentration of Cr3+(aq)Cr^{3+}(aq) increases.

Question 9

HardPaper 2 · calculator23 marks
(a)

A sample of chlorine consists of two isotopes, 35Cl^{35}Cl and 37Cl^{37}Cl.

(a) Contrast the sub-atomic structure of these two isotopes.

[1]
(b)(i)

(b) (i) The sample of chlorine is analysed in a mass spectrometer, producing a spectrum for the Cl2+Cl_2^+ ion. The spectrum shows three peaks at m/z values of 70, 72 and 74. Explain the origin and relative heights of these three peaks, given that the abundance of 35Cl^{35}Cl is approximately three times that of 37Cl^{37}Cl.

[3]
(b)(ii)

(ii) A more precise measurement finds the composition by mass to be: 35Cl^{35}Cl: 75.76%, 37Cl^{37}Cl: 24.24%. Calculate the relative atomic mass of chlorine from this sample, giving your answer to two decimal places. (Use isotopic masses of 35.0 and 37.0 for this calculation).

[2]
(c)(i)

Magnesium chloride, MgCl2MgCl_2, and manganese(II) chloride, MnCl2MnCl_2, are two ionic compounds.

(c) (i) Deduce the type of bonding in magnesium chloride, MgCl2MgCl_2, using electronegativity values from section 9 of the data booklet.

[2]
(c)(ii)

(ii) Determine the lattice enthalpy of magnesium chloride, assuming the bonding is purely ionic. Use sections 9, 10 and 12 of the data booklet and the following data:

Enthalpy of formation of magnesium chloride = −641 kJ mol−1-641 \text{ kJ mol}^{-1}

[3]
(c)(iii)

(iii) Explain, with reference to electron configurations, why the ionic radii of Mg2+Mg^{2+}, Mn2+Mn^{2+} and Cl−Cl^- are different. Use section 10 of the data booklet.

[3]
(c)(iv)

(iv) Predict, with a reason, which has the stronger ionic bonding, manganese(II) chloride, MnCl2MnCl_2, or magnesium chloride.

[2]
(d)(i)

Magnesium chloride is white, but manganese(II) chloride is pale pink.

(d) (i) State the condensed electron configuration of a manganese atom.

[1]
(d)(ii)

(ii) State the reason, in terms of electron configuration, why manganese(II) chloride is coloured.

[1]
(d)(iii)

(iii) Manganese(II) chloride absorbs light with a wavelength of approximately 530 nm. Describe why this is consistent with the observed colour of the compound. Use sections 2 and 15 of the data booklet.

[2]
(e)(i)

A copper key is to be electroplated with manganese using an aqueous solution of manganese(II) chloride as the electrolyte.

(e) (i) Deduce the half-equations for the reactions occurring at the anode (made of pure manganese) and the cathode (the copper key).

[2]
(e)(ii)

(ii) Deduce a balanced chemical equation for the reaction of fluorine gas with the aqueous chloride ions in the electrolyte.

[1]

Question 10

EasyPaper 2 · calculator1 mark

A student performs a redox titration where potassium permanganate solution is used to determine the concentration of an iron(II) salt. The overall balanced ionic equation for the reaction is shown below.

MnO4−(aq)+5Fe2+(aq)+8H+(aq)→Mn2+(aq)+5Fe3+(aq)+4H2O(l)MnO_4^- (aq) + 5Fe^{2+} (aq) + 8H^+ (aq) \rightarrow Mn^{2+} (aq) + 5Fe^{3+} (aq) + 4H_2O (l)

What is the oxidising agent in this reaction?

A. Fe2+Fe^{2+}

B. H+H^+

C. Mn2+Mn^{2+}

D. MnO4−MnO_4^-

Question 11

MediumPaper 2 · calculator1 mark

A student is performing various chemical reactions in the laboratory and needs to classify them based on whether electron transfer occurs. Which one of the following reactions is NOT a redox (reduction-oxidation) reaction?

A Mg(s)+2HCl(aq)→MgCl2(aq)+H2(g)Mg(s) + 2HCl(aq) \rightarrow MgCl_2(aq) + H_2(g)

B 2CH3CH2OH(aq)+O2(g)→2CH3CHO(aq)+2H2O(l)2CH_3CH_2OH(aq) + O_2(g) \rightarrow 2CH_3CHO(aq) + 2H_2O(l)

C FeCl3(aq)+3NaOH(aq)→Fe(OH)3(s)+3NaCl(aq)FeCl_3(aq) + 3NaOH(aq) \rightarrow Fe(OH)_3(s) + 3NaCl(aq)

D Cl2(g)+2NaOH(aq)→NaCl(aq)+NaClO(aq)+H2O(l)Cl_2(g) + 2NaOH(aq) \rightarrow NaCl(aq) + NaClO(aq) + H_2O(l)

Question 12

HardPaper 2 · calculator16 marks
(a)(i)

Strontium is an alkaline earth metal in group 2 of the periodic table, used to produce the red colour in fireworks.

(a) In a sample of strontium, 10.0% of the atoms have a mass number of 86 and the remainder have a mass number of 88.

(i) Deduce the nuclear symbol of the isotope of strontium with mass number 86. Use section 6 of the data booklet.

[1]
(a)(ii)

(ii) Calculate, to two decimal places, the relative atomic mass of this sample of strontium.

[2]
(a)(iii)

(iii) Explain why the first ionization energy of strontium is greater than that of rubidium.

[2]
(b)(i)

(b) Strontium nitrate has the formula Sr(NO3)2Sr(NO_3)_2.

(i) The compound contains both ionic and covalent bonds. State which particles are joined by covalent bonds and which are joined by ionic bonds.

[2]
(b)(ii)

(ii) Contrast covalent and ionic bonds in terms of how the valence electrons are involved.

[1]
(b)(iii)

(iii) Write a balanced chemical equation for the formation of strontium nitrate solution from the reaction of solid strontium hydroxide with nitric acid.

[2]
(b)(iv)

(iv) Calculate the volume, in cm3cm^3, of 1.50 mol dm−31.50 \text{ mol dm}^{-3} nitric acid required to react completely with 5.00 g5.00 \text{ g} of solid strontium hydroxide.

[3]
(b)(v)

(v) Predict, with a reason, whether strontium oxide is acidic, basic or amphoteric.

[1]
(b)(vi)

(vi) Describe an experiment to establish the relative reactivity of strontium and zinc using the metals and aqueous solutions of their nitrates.

[2]

Question 13

EasyPaper 2 · calculator1 mark

The following table provides standard electrode potentials (E⊖E^{\ominus}) for several half-reactions at 298 K.

Half-reactionE⊖E^{\ominus} / V
K+(aq)+e−⇌K(s)K^+(aq) + e^- \rightleftharpoons K(s)−2.93-2.93
Zn2+(aq)+2e−⇌Zn(s)Zn^{2+}(aq) + 2e^- \rightleftharpoons Zn(s)−0.76-0.76
Fe2+(aq)+2e−⇌Fe(s)Fe^{2+}(aq) + 2e^- \rightleftharpoons Fe(s)−0.45-0.45
2H+(aq)+2e−⇌H2(g)2H^+(aq) + 2e^- \rightleftharpoons H_2(g)0.000.00
I2(s)+2e−⇌2I−(aq)I_2(s) + 2e^- \rightleftharpoons 2I^-(aq)+0.54+0.54
Ag+(aq)+e−⇌Ag(s)Ag^+(aq) + e^- \rightleftharpoons Ag(s)+0.80+0.80
Cl2(g)+2e−⇌2Cl−(aq)Cl_2(g) + 2e^- \rightleftharpoons 2Cl^-(aq)+1.36+1.36
F2(g)+2e−⇌2F−(aq)F_2(g) + 2e^- \rightleftharpoons 2F^-(aq)+2.87+2.87

Which species is the strongest reducing agent?

A. K(s)K(s)

B. F2(g)F_2(g)

C. F−(aq)F^-(aq)

D. K+(aq)K^+(aq)

Question 14

MediumPaper 2 · calculator1 mark

Use the following table of standard reduction potentials to answer the question.

Half-reactionE⊖/VE^\ominus / \text{V}
F2(g)+2e−⇌2F−(aq)F_2(g) + 2e^- \rightleftharpoons 2F^-(aq)+2.87
Cl2(g)+2e−⇌2Cl−(aq)Cl_2(g) + 2e^- \rightleftharpoons 2Cl^-(aq)+1.36
MnO2(s)+4H+(aq)+2e−⇌Mn2+(aq)+2H2O(l)MnO_2(s) + 4H^+(aq) + 2e^- \rightleftharpoons Mn^{2+}(aq) + 2H_2O(l)+1.23
Br2(aq)+2e−⇌2Br−(aq)Br_2(aq) + 2e^- \rightleftharpoons 2Br^-(aq)+1.09
Ag+(aq)+e−⇌Ag(s)Ag^+(aq) + e^- \rightleftharpoons Ag(s)+0.80
I2(s)+2e−⇌2I−(aq)I_2(s) + 2e^- \rightleftharpoons 2I^-(aq)+0.54
Cu2+(aq)+2e−⇌Cu(s)Cu^{2+}(aq) + 2e^- \rightleftharpoons Cu(s)+0.34
Sn4+(aq)+2e−⇌Sn2+(aq)Sn^{4+}(aq) + 2e^- \rightleftharpoons Sn^{2+}(aq)+0.15
2H+(aq)+2e−⇌H2(g)2H^+(aq) + 2e^- \rightleftharpoons H_2(g)0.00
Fe2+(aq)+2e−⇌Fe(s)Fe^{2+}(aq) + 2e^- \rightleftharpoons Fe(s)-0.45
Zn2+(aq)+2e−⇌Zn(s)Zn^{2+}(aq) + 2e^- \rightleftharpoons Zn(s)-0.76
Mg2+(aq)+2e−⇌Mg(s)Mg^{2+}(aq) + 2e^- \rightleftharpoons Mg(s)-2.37

Which species in the table can oxidize bromide ions (Br−Br^-) to bromine (Br2Br_2)?

A. Cl2Cl_2 and F2F_2

B. Ag+Ag^+ and I2I_2

C. H+H^+ and Cu2+Cu^{2+}

D. ZnZn and MgMg

Question 15

EasyPaper 2 · calculator1 mark

In a laboratory experiment, a student is investigating various redox reactions. Which of the following changes requires a reducing agent?

A Cr2O72−→Cr3+Cr_2O_7^{2-} \rightarrow Cr^{3+}

B Fe2+→Fe3+Fe^{2+} \rightarrow Fe^{3+}

C I−→I2I^- \rightarrow I_2

D SO32−→SO42−SO_3^{2-} \rightarrow SO_4^{2-}

Question 16

MediumPaper 2 · calculator8 marks
(a)

A student investigates electrochemical cells using the following standard electrode potentials.

Half-equationE⊖/VE^\ominus / \text{V}
Zn2+(aq)+2e−⇌Zn(s)Zn^{2+}(aq) + 2e^- \rightleftharpoons Zn(s)−0.76-0.76
Fe2+(aq)+2e−⇌Fe(s)Fe^{2+}(aq) + 2e^- \rightleftharpoons Fe(s)−0.45-0.45
Cu2+(aq)+2e−⇌Cu(s)Cu^{2+}(aq) + 2e^- \rightleftharpoons Cu(s)+0.34+0.34
Ag+(aq)+e−⇌Ag(s)Ag^+(aq) + e^- \rightleftharpoons Ag(s)+0.80+0.80

(i) Identify the species that is the strongest oxidizing agent in the table.

(ii) Identify the species that is the strongest reducing agent in the table.

[2]
(b)

A voltaic cell is constructed using the zinc and copper half-cells under standard conditions.

(i) State the half-equation for the reaction occurring at the anode.

(ii) Calculate the standard cell potential, Ecell⊖E^\ominus_{cell}, in V.

[3]
(c)

Deduce, justifying your answer, whether a spontaneous reaction will occur when solid silver metal, Ag(s)Ag(s), is placed into a 1.00 mol dm−31.00 \text{ mol dm}^{-3} solution of iron(II) nitrate.

[3]

Question 17

EasyPaper 1A · calculator1 mark

What is the oxidation state of manganese in the permanganate ion, MnO4−MnO_4^-?

A. +2

B. +4

C. +7

D. +8

Question 18

MediumPaper 2 · calculator5 marks
(a)

Use the following table of standard reduction potentials to answer the questions.

E⊖/VE^{\ominus} / V

Na+(aq)+e−⇌Na(s)Na^+(aq) + e^- \rightleftharpoons Na(s) -2.71

Zn2+(aq)+2e−⇌Zn(s)Zn^{2+}(aq) + 2e^- \rightleftharpoons Zn(s) -0.76

Cr3+(aq)+3e−⇌Cr(s)Cr^{3+}(aq) + 3e^- \rightleftharpoons Cr(s) -0.74

Fe2+(aq)+2e−⇌Fe(s)Fe^{2+}(aq) + 2e^- \rightleftharpoons Fe(s) -0.45

2H+(aq)+2e−⇌H2(g)2H^+(aq) + 2e^- \rightleftharpoons H_2(g) 0.00

Cu2+(aq)+2e−⇌Cu(s)Cu^{2+}(aq) + 2e^- \rightleftharpoons Cu(s) +0.34

Cu+(aq)+e−⇌Cu(s)Cu^+(aq) + e^- \rightleftharpoons Cu(s) +0.52

I2(aq)+2e−⇌2I−(aq)I_2(aq) + 2e^- \rightleftharpoons 2I^-(aq) +0.54

Fe3+(aq)+e−⇌Fe2+(s)Fe^{3+}(aq) + e^- \rightleftharpoons Fe^{2+}(s) +0.77

Ag+(aq)+e−⇌Ag(s)Ag^+(aq) + e^- \rightleftharpoons Ag(s) +0.80

Cl2(aq)+2e−⇌2Cl−(aq)Cl_2(aq) + 2e^- \rightleftharpoons 2Cl^-(aq) +1.36

A student constructs a voltaic cell using standard zinc and iron electrodes immersed in solutions of their respective ions.

(a) Write the overall balanced chemical equation for the spontaneous reaction occurring in this cell, including state symbols.

[2]
(b)

(b) Calculate the standard cell potential, Ecell⊖E^{\ominus}_{cell}, for this voltaic cell.

[3]

Question 19

EasyPaper 1A · calculator1 mark

In which compound does manganese have an oxidation state of +7+7?

A. MnO2MnO_2

B. Mn2O3Mn_2O_3

C. KMnO4KMnO_4

D. MnSO4MnSO_4

Question 20

MediumPaper 2 · calculator6 marks
(a)

Butan-2-ol, CH3CH(OH)CH2CH3CH_3CH(OH)CH_2CH_3, is a secondary alcohol that can be oxidized using acidified potassium dichromate(VI) solution to produce an organic compound, X.

(a) Identify the organic compound X and state the colour change observed for the oxidizing agent.

[2]
(b)

(b) The structure of a compound can be confirmed using ¹H NMR spectroscopy. Predict the number of signals and the ratio of the areas under the signals for the ¹H NMR spectrum of butan-2-ol.

[2]
(c)

(c) Predict the number of signals and the ratio of the areas under the signals for the ¹H NMR spectrum of compound X.

[2]

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What does Electron transfer reactions cover in IB Chemistry?

This topic covers electron transfer reactions, including oxidation, reduction, and electrochemical cells. Oxidation is electron loss, an increase in oxidation state, or oxygen gain/hydrogen loss. Reduction is electron gain, a decrease in oxidation state, or oxygen loss/hydrogen gain.

Is Electron transfer reactions SL or HL?

Both. SL and HL students study Electron transfer reactions, and HL goes further: 3.2.12 The hydrogen half-cell `H⁺(aq) + e⁻ ⇌ ½H₂(g)` is assigned a standard electrode potential of zero by convention. It is used in the measurement of standard electrode potential, E⦵. Students interpret standard electrode potential data in terms of ease of oxidation and reduction.

How do I revise Electron transfer reactions for IB Chemistry?

Start from the core idea: this topic covers electron transfer reactions, including oxidation, reduction, and electrochemical cells. In the exam: oxidation state deduction is a 1-mark part in both papers. Balancing half-equations is 1 to 2 marks and the balance must be right in both atoms and charge. Then practise exam-style questions, easiest first, writing out every step of your working before you check it.

How does FourtyFive help me practise Electron transfer reactions?

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Yes. In the FourtyFive iPad app you write your working by hand with Apple Pencil, the way you would on paper, and it is marked the same way.

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