AQA · A-Level · Chemistry

    Course version: 7405 · Version from Sept 2016

    The relative solubilities of the sulfates of the elements Mg–Ba in water.

    Full specification wording

    Group 2, the alkaline earth metals: The relative solubilities of the sulfates of the elements Mg–Ba in water.

    Group 2 sulfates become less soluble down the group, the opposite way round from the hydroxides.

    Checked against the AQA 7405 specification (opens in a new tab) on .

    • Point 3 of 3
    • 3 key terms

    Study notes

    From the checked teaching notes for this specification point.

    The idea

    Group 2 sulfates become less soluble down the group, the opposite way round from the hydroxides. Magnesium sulfate dissolves freely, calcium sulfate is slightly soluble, and strontium and barium sulfates are effectively insoluble. This is why barium chloride is the reagent for detecting sulfate ions: Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s) gives a dense white precipitate. The solution must be acidified first with dilute hydrochloric acid to destroy carbonate ions, which would also give white precipitates. Nitric acid must not be used because it oxidises sulfite ions to sulfate ions, causing a false positive. Sulfuric acid must never be used, because it supplies the very ion being tested for. This insolubility makes barium sulfate safe as a barium meal, since it is opaque to X-rays and the toxic Ba²⁺ is not absorbed from the gut.

    What earns the marks

    • Stating that sulfate solubility decreases from magnesium to barium.
    • The ionic equation Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s).
    • The observation of a white precipitate.
    • Acidifying with dilute hydrochloric acid first, to remove carbonate ions.
    • Explaining that a barium meal is safe because barium sulfate is insoluble, so Ba²⁺ is not absorbed.

    Common mistakes and how to put them right

    • Assuming hydroxide and sulfate solubilities change the same way down the group, when they run in opposite directions.

    • Acidifying with sulfuric acid, which adds the very ion being tested for.

    • Acidifying with nitric acid, which oxidises sulfite to sulfate and gives a false positive.

    • Describing the barium sulfate precipitate as cream or yellow instead of white.

    • Treating barium sulfate as soluble and so predicting no precipitate.

    Exam tips

    • State the acid by name; 'acidify' on its own does not identify a reagent and loses the mark.
    • Keep the two Group 2 solubility trends on one line of revision notes, since questions often test them against each other.

    Try the lesson

    The start of the Group 2, the alkaline earth metals: The relative solubilities of the sulfates of the elements Mg–Ba in water. lesson, made from checked teaching notes for this specification point.

    Have a go first

    Which Group 2 sulfate is the most soluble in water?

    Listen

    Group 2 sulfates become less soluble down the group, the opposite way round from the hydroxides. Magnesium sulfate dissolves freely, calcium sulfate is slightly soluble, and strontium and barium sulfates are effectively insoluble. This is why barium chloride is the reagent for detecting sulfate ions: Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s) gives a dense white precipitate. The solution must be acidified first with dilute hydrochloric acid to destroy carbonate ions, which would also give white precipitates. Nitric acid must not be used because it oxidises sulfite ions to sulfate ions, causing a false positive. Sulfuric acid must never be used, because it supplies the very ion being tested for. This insolubility makes barium sulfate safe as a barium meal, since it is opaque to X-rays and the toxic Ba²⁺ is not absorbed from the gut. A strong answer earns marks for these points. stating that sulfate solubility decreases from magnesium to barium. the ionic equation Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s). the observation of a white precipitate. acidifying with dilute hydrochloric acid first, to remove carbonate ions. Exam tip: State the acid by name; 'acidify' on its own does not identify a reagent and loses the mark.

    See it

    A flowchart running from top to bottom. The first step is 'Add dilute hydrochloric acid', which leads to 'Carbonate ions destroyed'. This leads to 'Add barium chloride', which leads to the ionic equation 'Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s)', which leads to 'Dense white precipitate'. Separately, 'Sulfate solubility decreases Mg to Ba' leads to 'Barium sulfate effectively insoluble', which leads to 'Barium meal safe: Ba²⁺ not absorbed'.
    The sequence of steps in the sulfate ion test with barium chloride, and how the insolubility of barium sulfate makes a barium meal safe.

    Key words

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    Group 2 sulfate solubility

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    test for sulfate ions

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    barium sulfate precipitate

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    See every definition
    Group 2 sulfate solubility
    The sulfates of the elements Mg–Ba become less soluble in water down the group, the opposite way round from the hydroxides.
    test for sulfate ions
    Barium chloride is the reagent, giving a dense white precipitate of barium sulfate, and the solution must be acidified first with dilute hydrochloric acid.
    barium sulfate precipitate
    Formed as a dense white precipitate by Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s) when barium chloride is added to a solution containing sulfate ions.

    Label the diagram

    Some boxes have lost their names. Pick the right name for each number.

    The diagram again, with 3 boxes numbered instead of named. A flowchart running from top to bottom. The first step is 'Add dilute hydrochloric acid', which leads to 'Carbonate ions destroyed'. This leads to 'Add barium chloride', which leads to the ionic equation 'Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s)', which leads to 'Dense white precipitate'. Separately, 'Sulfate solubility decreases Mg to Ba' leads to 'Barium sulfate effectively insoluble', which leads to 'Barium meal safe: Ba²⁺ not absorbed'.
    • 1Box 1

    • 2Box 2

    • 3Box 3

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