Complete the electronic configuration of the copper(II) ion. 1s²2s²2p⁶
- (a)(i)Complete the electronic configuration of the copper(II) ion. 1s²2s²2p⁶[1]
- (a)(ii)State the colour of the solutions containing the following ions. • [Cu(H₂O)₆]²⁺(aq) • [CuCl₄]²⁻(aq)[1]
- (a)(iii)Octahedral complexes of Cu²⁺ with different ligands can have different colours. Explain why.[2]
- (b)Copper(I) and silver(I) salts are colourless. Suggest why.[2]
- (c)(i)Consider the following two equilibria and associated data values at 298 K. AgBr(s) ⇌ Ag⁺(aq) + Br⁻(aq) equilibrium 1 Ksp = 5.0 × 10⁻¹³ mol² dm⁻⁶ Ag⁺(aq) + 2NH₃(aq) ⇌ [Ag(NH₃)₂]⁺(aq) equilibrium 2 Kstab = 1.7 x 10⁷ mol⁻² dm⁶ The equilibrium constant for equilibrium 1 is the solubility product, Ksp, of AgBr(s). The equilibrium constant for equilibrium 2 is the stability constant, Kstab, for the formation of [Ag(NH₃)₂]⁺(aq). Calculate the solubility of AgBr at 298 K in mol dm⁻³. solubility of AgBr =[1]
- (c)(ii)Use Le Chatelier's principle as applied to equilibria 1 and 2 to suggest why AgBr(s) dissolves in concentrated NH₃(aq).[2]
- (c)(iii)Use equilibria 1 and 2 to construct an equation for the reaction of AgBr(s) with concentrated NH₃(aq). This is equilibrium 3. equilibrium 3[1]
- (c)(iv)Write an expression for the equilibrium constant of equilibrium 3, Keq3, in terms of Ksp for equilibrium 1 and Kstab for equilibrium 2. Keq3 =[1]
- (d)Define the term standard electrode potential, Eᵒ.[1]
- (e)(i)Complete and label the diagram to show how the standard electrode potential, Eᵒ, of Ag⁺(aq)/Ag(s) could be measured under standard conditions. [Figure X.X][4]
- (e)(ii)Use the Data Booklet to label the diagram in (e)(i) to show: • which is the positive electrode, • the direction of electron flow in the external circuit when a current flows.[1]
This question uses a diagram from the original paper, which isn't shown here. Open the full paper from the past papers archive to see it.
Mark scheme
Marking points from the official mark scheme (May/June 2019). The mark or mark type is shown in brackets.
- [1] 3s²3p⁶3d⁹
- [1] [Cu(H₂O)₆]²⁺ (pale) blue; CuCl₄²⁻ yellow; both [1]
- [1] M1 energy gap / ΔE is different (for the ligands)
- [1] M2 different frequency / wavelength of light absorbed / transmitted / reflected
- [1] M1 (Cu⁺/Ag⁺) d-shell is full / complete OR d-orbitals are full
- [1] M2 no electrons can be promoted
- [1] solubility = √5.0 × 10⁻¹³ = 7.1 x 10⁻⁷ (mol dm⁻³) min 2sf
- [1] M1 (in conc. NH₃) [NH₃] increases and equilibrium 2 shifts to the right
- [1] M2 [Ag⁺] decreases and equilibrium 1 shifts to the right
- [1] AgBr + 2NH₃ = [Ag(NH₃)₂]⁺ + Br⁻
- [1] Keq3 = Ksp × Kstab ALLOW Keq3= [Ag(NH₃)₂⁺][Br⁻]/[NH₃]²
- [1] The potential difference when a half-cell is connected to a (standard) hydrogen electrode under standard conditions OR the potential difference / voltage / EMF between a hydrogen electrode and another half-cell under standard conditions
- [4] salt bridge • voltmeter / V • Ag • Ag⁺ (or soluble silver salt) • Pt • H₂ (and delivery correct) + H⁺ (or named strong acid) • 1 atm. (pressure) • 1 mol dm⁻³ (and 298 K) • mark as ✓✓✓✓
- [1] Ag electrode labelled and arrow (in the external circuit moving towards this electrode)
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