Fe2+ and Fe3+ ions are able to form a variety of complexes with different species.
- (a)(i)Define complex.[1]
- (a)(ii)Table 3.1 gives some details of different complexes of Fe2+ and of Fe3+. Complete Table 3.1. Table 3.1 complex ion ligand coordination number formula and charge of complex E Fe2+ NH3 6 F [FeC14]2- G en [Fe(en)3]3+[3]
- (a)(iii)Complete Fig. 3.1 to show the splitting of the d-orbitals in a tetrahedral complex. [Figure 3.1] energy[1]
- (b)(i)Table 3.2 gives details of some complexes of Fe3+. Table 3.2 complex colour value of Kstab [Fe(H2O)6]3+ violet 1 [Fe(H2O)5SCN]2+ red 1.40 x 102 [Fe(H2O)5F]2+ colourless 2.40 x 105 Explain the reason for the difference in colour of the two complexes [Fe(H2O)6]3+ and [Fe(H2O)5SCN]2+.[2]
- (b)(ii)Write an expression for Kstab of [Fe(H2O)5SCN]2+. Kstab = .......................................................................................................................................[1]
- (b)(iii)Use information in Table 3.2 to calculate the value of the equilibrium constant, Kc, for the following reaction. [Fe(H2O)5SCN]2+ + F¯ ⇌ [Fe(H2O)5F]2+ + SCN- Kc = ..............................................[1]
- (b)(iv)A few drops of KF(aq) are added to a solution of [Fe(H2O)6]3+(aq), followed by a few drops of KSCN(aq). Use information in Table 3.2 to describe any observations after each addition. Explain your answer.[2]
- (c)(i)Hydrated compound J, K3Fe(C2O4)3•xH2O, contains the green complex ion [Fe(C2O4)3]³¯. The value of x can be determined by titration of a sample of J with acidified MnO4¯ions. MnO4 ions oxidise C2O42- ions in acidic conditions. 2MnO4¯ + 5C2O42- + 16H+ → 2Mn2+ + 10CO2 + 8H2O Write half equations for the oxidation of C2O42- ions and for the reduction of MnO4¯ ions. • oxidation of C2O42- • reduction of MnO4¯[2]
- (c)(ii)A student prepares a solution containing 0.100 g of J. The student titrates this solution with 0.0200 moldm⁻³ acidified KMnO4(aq). The titre obtained is 12.20 cm³. Assume all of the C2O42– ions are oxidised. Calculate the value of x in K3Fe(C2O4)3•XH2O. Give your answer to the nearest whole number. Show your working. [Mr: K3Fe(C2O4)3, 437.1] x = ..............................................[4]
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Mark scheme
Marking points from the official mark scheme (Feb/Mar 2025). The mark or mark type is shown in brackets.
- [1] (central) metal / transition element atom / ion AND surrounded by / bonded to ligands
- [3] complex E: [Fe(NH3)6]2+
- complex F: Fe2+, Cl-, 4
- complex G: Fe3+, 6
- any two [1] any four [2] all six [3]
- [1] three(3) higher AND two(2) lower boxes / energy levels
- [1] d-d energy gap / ΔE is different
- [1] different frequency / wavelength (of light) absorbed / transmitted / reflected
- [1] Kstab = [[Fe(H₂O)₅SCN]²⁺] / ([[Fe(H₂O)₆]³⁺] [SCN⁻]])
- [1] Kc = 2.40 x 105 / 1.40 × 102 = 1714 min 2sf
- [2] M1: solution turns (violet / purple to) colourless AND solution then remains / stays colourless / no change
- M2: Kstab of [Fe(H2O)5F]2+ > [Fe(H2O)5SCN]2+ OR [Fe(H2O)5F]2+ is most stable (more stable than [Fe(H2O)5SCN]2+)
- [2] C2O42- → 2CO2 + 2e-
- MnO4- + 8H+ + 5e- → Mn2+ + 4H2O
- [4] M1 moles of manganate = 12.20/1000 × 0.0200 = 2.44 x 10-4 mol AND moles of ethanedioate = 5/2 x 2.44 × 10-4 = 6.10 x 10-4 mol
- M2 moles of K3Fe(C2O4)3 = 6.10 × 10-4 ÷ 3 = 2.03 × 10-4 mol AND mass of K3Fe(C2O4)3 = 437.1 x 2.03 × 10-4 = 0.0889 g
- M3 mass of water = 0.100 -0.0889 = 0.0111 g AND moles of water = 0.0111/18.0 = 6.18 x 10-4 mol
- M4 x = molar ratio = 6.18 x 10-4/2.03 × 10-4 = 3
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