The following table lists the solubilities of the hydroxides and carbonates of some of the Group 2 elements, M, at 25 °C. solubility/mol dm⁻³ element M M(OH)₂ MCO₃ Mg 2.0 × 10⁻⁴ 1.5 x 10⁻³ Ca 1.5 x 10⁻² 1.3 x 10⁻⁴ Sr 3.4 x 10⁻² 7.4 x 10⁻⁵ Ba 1.5 x 10⁻¹ 9.1 x 10⁻⁵
- (a)(i)Explain why the solubility of the Group 2 hydroxides, M(OH)₂, increases down the group.[3]
- (a)(ii)Suggest a reason for the general decrease in the solubility of the Group 2 carbonates, MCO₃, down the group.[1]
- (a)(iii)When carbon dioxide is passed through a saturated solution of calcium hydroxide (limewater), a white precipitate of calcium carbonate is formed. Use the data in the table to deduce, for each of Mg, Sr and Ba, whether or not a saturated solution of its hydroxide could also be used to test for carbon dioxide. Explain your answer. No calculations are required.[2]
- (b)(i)Calculate the value of the solubility product, Ksp, of magnesium hydroxide at 25°C. Ksp =[2]
- (b)(ii)State what would be observed if a few drops of a saturated solution of barium hydroxide are added to a saturated solution of barium carbonate. Explain your answer. observation explanation[2]
- (c)The equation for the formation of the gaseous hydroxide ion is shown. ½H₂(g) + ½O₂(g) + e⁻ → OH⁻(g) ΔH = ΔHᶠ(OH⁻(g)) Use data in the table and from the Data Booklet to calculate ∆Hᶠ(OH⁻(g)). You might find it useful to construct a Born-Haber cycle. enthalpy change ∆Hᶠ/kJ mol⁻¹ atomisation of Mg(s) +148 formation of Mg(OH)₂(s) -925 lattice energy of Mg(OH)₂(s) -2993 ΔHᶠ(OH⁻(g)) = kJ mol⁻¹[3]
Mark scheme
Marking points from the official mark scheme (Feb/Mar 2019). The mark or mark type is shown in brackets.
- [3] M1 ∆Hlatt and ∆Hhyd both decrease OR ∆Hlatt and ∆Hhyd both become less exothermic / more endothermic
- M2 ∆Hlatt decreases more than ∆Hhyd (as OH⁻ smaller than M²⁺)
- M3 ∆Hsol becomes more exothermic / more negative
- [1] (for MCO3) change / decrease in ∆Hhyd is larger than decrease in ∆Hlatt
- [2] M1 Sr and Ba could be used AND Mg could not be used
- M2 solubility of MgCO₃ is more than Mg(OH)₂ OR SrCO₃ / BaCO₃ is less than Sr(OH)₂ / Ba(OH)₂
- [2] Ksp = [Mg²⁺(aq)][OH⁻(aq)]² OR Ksp = (2.0 × 10⁻⁴)(4.0 × 10⁻⁴)²
- = 3.2 x 10⁻¹¹
- [2] M1 (white) ppt. / solid (of BaCO₃) will appear
- M2 due to the common ion effect OR the BaCO₃(s) ⇌ Ba²⁺(aq) + CO₃²⁻(aq) equilibrium shifts to the left
- [3] X Mg²⁺(g) + 2OH⁻(g)
- elements
- LE
- ΔHᶠ
- Mg(OH)₂(s)
- -2993 + 148 + 736 + 1450 + 2∆Hᶠ(OH⁻(g)) = -925
- 2∆Hᶠ(OH⁻(g)) = -266
- ΔHᶠ(OH⁻(g)) = -133 (kJ mol⁻¹)
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