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Questions on Group 2 compounds: solubility, uses and the sulfate test
The solubility of the Group 2 hydroxides increasing down the group and of the sulfates decreasing, magnesium hydroxide as an antacid, calcium hydroxide on acid soil, calcium oxide and calcium carbonate in flue-gas desulfurisation, barium sulfate as a barium meal, the thermal decomposition of calcium carbonate, the test for sulfate ions with acidified barium chloride and why the acid is added, the tests that identify Mg²⁺, Ca²⁺, Sr²⁺ and Ba²⁺, flame colours for Group 2 and for lithium, sodium and potassium, the thermal decomposition of the Group 2 carbonates and nitrates and the rise in their stability down the group explained by polarising power, the Group 1 carbonates and nitrates compared, and the procedure for comparing how easily they decompose.
22 original questions · 77 marks · the Group 2 compounds: solubility, uses and the sulfate test notes · Group 2 and Group 7 · Flashcards for this unit
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Describe how sodium hydroxide solution and dilute sulfuric acid could be used to identify which of four solutions contains Mg²⁺, Ca²⁺, Sr²⁺ and Ba²⁺ ions. Give the expected observations and explain them.
Mark scheme
Indicative content
- add sodium hydroxide solution dropwise to a sample of each solution, and dilute sulfuric acid to a fresh sample of each
- with sodium hydroxide, Mg²⁺ gives a white precipitate, Ca²⁺ a slight white precipitate, and Sr²⁺ and Ba²⁺ little or none
- with dilute sulfuric acid, Ba²⁺ gives a dense white precipitate, Sr²⁺ a white precipitate, Ca²⁺ a slight one and Mg²⁺ none
- the hydroxide results follow because hydroxide solubility increases down the group, so magnesium hydroxide precipitates most
- the sulfate results follow because sulfate solubility decreases down the group, so barium sulfate precipitates most
- a correct ionic equation, such as Mg²⁺(aq) + 2OH⁻(aq) → Mg(OH)₂(s) or Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s)
Levels
- Level 3 (5–6 marks) both reagents are used on separate samples, the observations for all four ions with each reagent are given, both trends in solubility are used to explain them, and a correct ionic equation is written; the answer would let a student tell the four solutions apart
- Level 2 (3–4 marks) the observations with both reagents are mostly right and one solubility trend explains them; the other trend or the ionic equation is not there
- Level 1 (1–2 marks) a white precipitate is mentioned for one ion; the two solubility trends are often run the same way, with barium hydroxide called the least soluble
Describe the trends in solubility of the Group 2 hydroxides and sulfates shown in the bar chart, and explain how the hydroxide trend affects the pH of their saturated solutions.
The solubility of each hydroxide and each sulfate at room temperature, on a logarithmic scale: each gridline up is ten times more soluble than the one below. Mark scheme
- B1 the hydroxides become more soluble down the group, Mg(OH)₂ being sparingly soluble
- B1 the sulfates become less soluble down the group, BaSO₄ being insoluble
- B1 a more soluble hydroxide puts a higher concentration of hydroxide ions into its saturated solution
- B1 so the pH of the saturated solution rises down the group, from about 10 for Mg(OH)₂ to about 13 for Ba(OH)₂
Give one use each of magnesium hydroxide, calcium hydroxide, calcium oxide and barium sulfate, and the property of each compound that makes it suitable.
Mark scheme
- B1 magnesium hydroxide treats indigestion: it neutralises excess stomach acid, and is sparingly soluble so the hydroxide concentration stays low
- B1 calcium hydroxide treats acidic soil: it is a base that neutralises the acid and raises the pH
- B1 calcium oxide removes sulfur dioxide from flue gases: it is a basic oxide that reacts with the acidic gas
- B1 barium sulfate is the barium meal: it is insoluble, so toxic Ba²⁺ is not absorbed, and barium absorbs X-rays
Explain why barium sulfate is given as a suspension for a barium meal, although barium ions are toxic, while magnesium sulfate (Epsom salts) can be taken dissolved in water.
Mark scheme
- B1 barium sulfate is insoluble, so it cannot form a solution and is swallowed as a suspension of solid
- B1 because it does not dissolve, barium ions are not released and are not absorbed into the blood; reject 'barium sulfate is not toxic'
- B1 barium absorbs X-rays strongly, so the gut lined with barium sulfate shows up on the X-ray
- B1 magnesium sulfate is soluble and dissolves, and magnesium ions are not toxic at that dose
Describe how to test a solution for sulfate ions, giving the reagents, the positive result and the ionic equation, with state symbols, for the reaction.
Mark scheme
- B1 add dilute hydrochloric acid (or dilute nitric acid) to the solution first; reject sulfuric acid
- B1 then add a few drops of barium chloride solution; allow barium nitrate
- B1 a white precipitate shows that sulfate ions are present; ignore 'cloudy' unless a precipitate is named
- B1 Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s)
Explain why the solution is acidified before barium chloride is added in the sulfate test, why sulfuric acid cannot be the acid, and why fizzing when the acid is added does not spoil the test.
Mark scheme
- B1 the acid removes carbonate ions, reacting with them to form carbon dioxide and water
- B1 otherwise carbonate ions would form a white precipitate of barium carbonate, giving a false positive; reject 'removes impurities'
- B1 sulfuric acid contains sulfate ions, so a white precipitate would form whether or not the sample contained sulfate
- B1 fizzing shows that carbonate was present; once it has been removed, a white precipitate still shows sulfate
Evaluate the use of calcium carbonate rather than calcium oxide to remove sulfur dioxide from power-station flue gases.
Mark scheme
- B1 both react with sulfur dioxide to form calcium sulfite, so both remove it
- B1 calcium carbonate releases carbon dioxide at the scrubber: CaCO₃(s) + SO₂(g) → CaSO₃(s) + CO₂(g)
- B1 calcium oxide is made by heating calcium carbonate, which releases the same carbon dioxide at the kiln and uses energy
- B1 so calcium carbonate is cheaper and releases no more carbon dioxide overall, which makes it the better choice
Describe how to compare the thermal stabilities of magnesium carbonate and calcium carbonate in the laboratory, including how to make the test fair and how to avoid suck-back.
Mark scheme
- B1 heat the same amount in moles of each carbonate in identical boiling tubes, with a delivery tube leading into limewater
- B1 use the same Bunsen flame at the same height and the same volume of limewater for each
- B1 time how long it takes for the limewater to turn milky; the shorter the time, the less stable the carbonate
- B1 lift the delivery tube out of the limewater before removing the flame, so cold limewater is not drawn back into the hot tube
Describe a test, with its positive result, for each of hydrogen, oxygen, chlorine and sulfur dioxide.
Mark scheme
- B1 hydrogen: a lighted splint at the mouth of the tube gives a squeaky pop
- B1 oxygen: a glowing splint placed in the gas relights
- B1 chlorine: damp blue litmus paper turns red and is then bleached white; allow damp litmus is bleached
- B1 sulfur dioxide: acidified aqueous potassium manganate(VII) turns from purple to colourless; allow acidified potassium dichromate(VI) turning from orange to green
Explain how a student could show that a solution of an unknown salt contains nitrate ions, using sodium hydroxide solution and aluminium foil, and why sodium hydroxide is first warmed with the solution on its own.
Mark scheme
- B1 warm the solution with sodium hydroxide alone and test for ammonia with damp red litmus, so that ammonia from any ammonium ions is detected and driven off first
- B1 then add aluminium foil, or Devarda's alloy, and warm again
- B1 a gas that turns damp red litmus paper blue is ammonia, and shows that nitrate ions were present
- B1 aluminium reduces the nitrogen from +5 in NO₃⁻ to −3 in NH₃, so the ammonia can only have come from nitrate
Show that the concentration of sulfate ions in a solution is 0.100 mol dm⁻³, given that excess barium chloride solution added to 25.0 cm³ of it gives 0.583 g of dry barium sulfate. Ar values: Ba 137.3, S 32.1, O 16.0.
Mark scheme
- M1 Mr of BaSO₄ = 137.3 + 32.1 + 4 × 16.0 = 233.4
- M1 n(BaSO₄) = 0.583 ÷ 233.4 = 2.50 × 10⁻³ mol
- M1 Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s), and barium chloride is in excess, so n(SO₄²⁻) in the 25.0 cm³ sample = 2.50 × 10⁻³ mol
- A1 concentration = 2.50 × 10⁻³ ÷ 0.0250 = 0.100 mol dm⁻³, with the working shown in full because the answer is given
Calculate the volume, in cm³, of 0.0500 mol dm⁻³ hydrochloric acid neutralised by a tablet containing 0.350 g of magnesium hydroxide. Ar values: H 1.0, O 16.0, Mg 24.3.
Mark scheme
- M1 Mr(Mg(OH)₂) = 58.3, so amount of Mg(OH)₂ = 0.350 ÷ 58.3 = 6.003 × 10⁻³ mol
- M1 Mg(OH)₂(s) + 2HCl(aq) → MgCl₂(aq) + 2H₂O(l), so amount of HCl = 2 × 6.003 × 10⁻³ = 1.201 × 10⁻² mol
- A1 volume = 1.201 × 10⁻² ÷ 0.0500 = 0.240 dm³ = 240 cm³, to three significant figures
Calculate the mass of calcium oxide, in tonnes, needed to remove 2.50 tonnes of sulfur dioxide from flue gases. Ar values: O 16.0, S 32.1, Ca 40.1.
Mark scheme
- M1 Mr(SO₂) = 64.1, so amount of SO₂ = 2.50 × 10⁶ g ÷ 64.1 = 3.900 × 10⁴ mol
- M1 CaO(s) + SO₂(g) → CaSO₃(s) is 1 : 1, and Mr(CaO) = 56.1, so mass = 3.900 × 10⁴ × 56.1 g
- A1 2.19 × 10⁶ g, which is 2.19 tonnes to three significant figures
Identify the Group 2 ion, Mg²⁺, Ca²⁺ or Ba²⁺, in each of solutions P, Q and R from the results in the table.
Solution With sodium hydroxide solution With dilute sulfuric acid P White precipitate No change Q No change Dense white precipitate R Slight white precipitate Slight white precipitate Mark scheme
- B1 P contains Mg²⁺, since magnesium hydroxide is only sparingly soluble and magnesium sulfate is soluble
- B1 Q contains Ba²⁺, since barium hydroxide is soluble and barium sulfate insoluble
- B1 R contains Ca²⁺, since calcium hydroxide and calcium sulfate are both sparingly soluble
Suggest why a student who added barium chloride solution to tap water from a limestone area saw a white precipitate, and what she should do to find out whether the water contains sulfate ions.
Mark scheme
- B1 water from a limestone area contains carbonate (or hydrogencarbonate) ions
- B1 these form a white precipitate of barium carbonate, so the result does not show sulfate
- B1 repeat the test after adding dilute hydrochloric acid until fizzing stops; a white precipitate then shows sulfate
Compare the results obtained when sodium hydroxide solution and dilute sulfuric acid are added separately to solutions of magnesium chloride and barium chloride.
Mark scheme
- B1 with sodium hydroxide, magnesium chloride gives a white precipitate but barium chloride gives no change
- B1 with dilute sulfuric acid, barium chloride gives a white precipitate but magnesium chloride gives no change
- B1 the results are opposite because hydroxide solubility increases down the group while sulfate solubility decreases
Explain why barium carbonate needs a higher temperature to decompose than magnesium carbonate.
Mark scheme
- B1 the Ba²⁺ ion is larger than the Mg²⁺ ion and has the same charge, so its charge density is lower
- B1 Ba²⁺ polarises (distorts) the electron cloud of the carbonate ion less, so the C–O bonds in the anion are weakened less
- B1 more energy is needed to break the carbonate ion into an oxide ion and carbon dioxide, so a higher temperature is needed
Calculate the volume of oxygen, in cm³ at room temperature and pressure, given off when 1.48 g of magnesium nitrate is fully decomposed by heating. Ar values: N 14.0, O 16.0, Mg 24.3; molar gas volume = 24.0 dm³ mol⁻¹.
Mark scheme
- M1 Mr(Mg(NO₃)₂) = 24.3 + 2 × (14.0 + 3 × 16.0) = 148.3, so amount = 1.48 ÷ 148.3 = 9.980 × 10⁻³ mol
- M1 2Mg(NO₃)₂(s) → 2MgO(s) + 4NO₂(g) + O₂(g), so amount of O₂ = 9.980 × 10⁻³ ÷ 2 = 4.990 × 10⁻³ mol
- A1 volume = 4.990 × 10⁻³ × 24.0 = 0.120 dm³ = 120 cm³, to three significant figures
Identify the anion in each of solutions X, Y and Z from the results in the table.
Solution Test Result X Dilute hydrochloric acid added Effervescence; the gas turns limewater milky Y Ba²⁺(aq), then excess dilute hydrochloric acid White precipitate dissolves; the gas decolourises acidified manganate(VII) Z Ba²⁺(aq), then excess dilute hydrochloric acid White precipitate that does not dissolve Mark scheme
- B1 X contains carbonate ions, CO₃²⁻, because the gas given off with acid is carbon dioxide
- B1 Y contains sulfite ions, SO₃²⁻, because barium sulfite dissolves in acid and gives sulfur dioxide, which reduces manganate(VII)
- B1 Z contains sulfate ions, SO₄²⁻, because barium sulfate is insoluble even in excess acid
Suggest why damp blue litmus paper held in chlorine turns red and then white, while damp blue litmus paper held in sulfur dioxide turns red and stays red.
Mark scheme
- B1 chlorine reacts with the water on the paper to give hydrochloric acid and chloric(I) acid, which turn the litmus red
- B1 chloric(I) acid is an oxidising agent and bleaches the dye, so the paper turns white
- B1 sulfur dioxide dissolves to give sulfuric(IV) acid, which is acidic and turns the litmus red but does not oxidise the dye, so it stays red
Suggest why barium hydroxide would not be suitable as an indigestion remedy in place of magnesium hydroxide.
Mark scheme
- B1 barium hydroxide is soluble, so it would give a high concentration of hydroxide ions, a strongly alkaline solution that would damage the gut
- B1 it would release toxic Ba²⁺ ions into solution, to be absorbed into the blood
Suggest why heating lithium nitrate gives a brown gas but heating sodium nitrate does not.
Mark scheme
- B1 Li⁺ is a very small ion with a high charge density, so it polarises the nitrate ion strongly, as a Group 2 ion does, and the nitrate decomposes to the oxide, brown nitrogen dioxide and oxygen
- B1 Na⁺ is larger, so it polarises the nitrate ion less and sodium nitrate only loses oxygen, forming sodium nitrite with no nitrogen dioxide
Practise Group 2 compounds: solubility, uses and the sulfate test one question at a time