3B _ 6B -Test for ions 2013

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    LAS Chemistry Practicals (3B) 2012 - 2013 T.A. Aoudi

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    Test For gases

    GAS OBSERVATIONS

    Oxygen O2A colourless gas that:Relights a glowing splint

    Carbon dioxide CO2

    gives a white ppt. with limewater.

    CO2(g) + Ca(OH)2(aq) CaCO3(s) + H2O(l)White ppt.

    Sulfur dioxide SO2

    A colourless acidic gas which:

    Turns a filterpaper soaked with acidified potassium dichromate(VI),

    K2Cr2O7from orangeto green.

    3SO2 (g) + Cr2O72

    (g) + 2H+ 2Cr

    3++ 3SO4

    2+ H2O

    Orange GreenOR

    decolourises a filter papersoaked with acidified purple KMnO4solution.

    Hydrogen sulfide H2S smells like a rotteneggs.The gas turns lead(II) ethanoate paper from white to black.

    Pb2+

    + S2

    PbS

    black

    ammonia NH3

    has a pungent orchoking smell.

    The gas turns moist red litmus paperblue.

    OR Produces white fumes with HClvapour

    NH3(g) + HCl(g) NH4Cl(s)

    Nitrogen dioxide NO2

    A brown acidic gas which:

    decolourises a filterpaper soaked with acidified purple KMnO4solution.

    OR

    gives a colourless solution in water which remains colourless uponaddition of NaOH

    hydrogen H2A colouless gas which:

    ignites with a pop with a lighted splint.

    H2(g) + O2(g) H2O(l)

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    Hydrogen chloride HCl

    Gives steamy fumes when exposed to moist air;

    acidic gas Turns damp blue litmus paperred. Produces white fumes withNH3(g) vapour

    NH3(g) + HCl(g)

    NH4Cl(s)

    Hydrogen bromide HBr Gives steamy fumes when exposed to moist air;

    acidic gas Turns damp blue litmus paperred. Produces white fumes withNH3(g) vapour

    NH3(g) + HBr(g) NH4Br(s)

    Chlorine Cl2

    A pale greenchoking gas whichbleaches moist litmus paper

    ORliberates orange Br2(aq)from a solutionofKBr

    Cl2 + 2Br Br2(aq) + 2Cl(aq)orange

    bromine Br2 Brown fumes

    iodine I2 Purple fumes

    Water vapourH2O

    Turns anhydrous cobalt (II)chloride CoCl2 paper from

    bluetopink.

    Turns anhydrous copper(II) sulfate, CuSO4 from white to blue

    Gases may be evolved on heating the solid

    GAS POSSIBLE SOURCE

    CO2Carbonates or hydrogen carbonates of metals other than Group 1.

    CaCO3 heat CaO + CO2(g)

    NH3 Ammonium salts NH4Br(s) heat NH3(g) + HBr(g)

    O2 aloneGroup 1 nitrate [ other than Li]

    KNO3(s) heat KNO2(s) + O2(g)

    O2 & NO2

    brown fumes

    Nitrates [other than Na or K]Mg(NO3)2 (s) heat MgO(s) + 2NO2(g) + O2(g)

    Hydrogen chloride

    HCl(g)

    Hydrated chlorides or ammonium chloride

    NH4Cl(s) heat NH3 + HCl(g)

    Water vapour

    H2O(g)

    Hydrated salt, hydrogen carbonate and otheracid salts.

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    Testing gases

    glowing splint

    relights

    Limewater

    turns milky

    CO2(g)

    O2(g) H2(g)

    Burning

    splint

    NH3(g)

    Pop

    sound

    damp redlitmus turns

    blue

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    Test of Anions

    Anion Test Test Result

    CarbonateCO3

    2

    pH > 10

    Add dilute acid

    OR

    Add CaCl2(aq)

    orMgSO4(aq) solution

    Effervescence , CO2 gas is produced.Then test for CO22H

    +(aq) + CO32

    CO2(g) + H2O(l)

    Ca2+

    + CO32

    CaCO3(s)white ppt

    Hydrogencar-bonate

    HCO3

    PH = 8 - 9 )

    Add dilute acid

    OR

    Add CaCl2(aq)orMgSO4(aq) solution

    Effervescence , CO2 gas is produced

    H+(aq) + HCO3

    CO2(g) + H2O(l)

    A white ppt confirms CO3

    2

    No ppt. in the cold ,but a white ppt onwarming confirms the presence ofHCO3

    Sulfate(VI)

    SO42

    Add

    Ba2+

    (aq)i.e Ba(NO3)2then

    followed by dilute HCl

    OR

    use Sr2+

    orPb(NO3)2(aq)

    White ppt.which is insolublein excessdilute strong acid ,HCl.

    Ba2+

    + SO42

    BaSO4(s)White ppt.

    SrSO4 and PbSO4 are insoluble;

    Sulfite

    SO32

    AddBa

    2+(aq)then followed by

    dilute HCl

    White ppt.[solublein excess dilute strong acid to give

    coloulress solution]

    Ba2+

    + SO32

    BaSO3(s)White ppt.

    SO2 is liberated with dilute acidsBaSO3 + 2HCl BaCl2(aq) + H2O + SO2

    Nitrate

    NO3

    Add aq. NaOH , thenaluminium foil [Devardas

    alloy]

    warm gently

    Ammonia gas

    NH3is liberated which turns dampredlitmus blue.

    NH4+

    + OH

    heat

    NH3(g) + H2O

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    NH4+

    Howto testfornitratesions NO3?

    Test : Add sodium hydroxide solution NaOH (aq) and aluminium foil to thesolution containing the nitrate ions.

    Result : damp RED litmus turns BLUE

    (alkaline) Ammonia gas is produced

    The aluminium foilreduces NO3 to ammonium ion NH4

    + which reacts with

    hydroxide to produce NH3(g) gas and water.

    NH4+

    (aq) + OH

    (aq) heat NH3(g) + H2O(l)

    Barium chloride ornitrate solution

    BaCl2(aq) forms precipitate of insoluble barium salts with a number of anions:

    Anion ppt . Addi t ion o f di lu te HCl

    Colour formula

    Sulfate; SO42 White BaSO4 The ppt. is insoluble

    Sulfite; SO32 White BaSO3The ppt. dissolvesto give SO2(g) an acidic gas .

    Carbonate;CO32 White BaCO3 The ppt. dissolves with effervescence& a colourless solution BaCl2(aq)

    Aluminiumpowder

    AmmoniaNH3gas

    NO3

    Damp red litmus

    paper turns blue

    heat heat

    NH4+

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    Halide ions

    Chloride

    Cl-

    Add HNO3/AgNO3(aq)

    OR

    Giveswhite ppt.(AgCl) with Ag+(aq) whichis soluble in dilute & Conc. NH3

    Ag

    +

    (aq) + Cl

    (aq)

    AgCl(s)

    Add HNO3 / Pb(NO3)2(aq) Pb2+(aq) + 2Cl(aq) PbCl2 (s)

    white ppt

    Bromide

    Br -

    Add HNO3/AgNO3(aq)

    OR

    Add HNO3 / Pb(NO3)2(aq)

    Givespale cream ppt.with Ag+(aq) which is :Ag

    +(aq) + Br

    (aq) AgBr(aq)

    o partially soluble inNH3(aq)o completely soluble in conc.NH3

    Pb2+

    (aq) + 2Br(aq) PbBr2(aq)off-white ppt

    Iodide

    I -

    Add HNO3/AgNO3(aq)

    OR

    Add HNO3 / Pb(NO3)2(aq)

    GivesPale yellow ppt.with Ag+(aq)Which isinsoluble in dilute orconc.NH3(aq)

    Ag+(aq) + I

    (aq) AgI(s)AgI isinsoluble in both concentrated and diluteammonia NH3

    Pb2+ (aq) + 2 I(aq) PbI2 (s)bright yellow ppt.

    Effect of aq.

    AgNO3 Effect of aq. (dilute)NH3 Effect ofConc. ammonia

    Cl(aq)

    chloride

    Whi te ppt .

    AgCl

    The ppt. dissolves forming acolourless solution

    AgCl + 2NH3(aq)

    [Ag(NH3)2]+(aq) + Cl

    (aq)

    The ppt . dissolves forminga colourless solution

    AgCl+ 2NH3(conc.)

    [Ag(NH3)2]+(aq) + Cl

    (aq)

    Br(aq)

    Bromide

    Cream pp t.AgBr

    remains insolubleThe ppt. is Soluble & dissolves

    forming a colourless solution

    AgBr + 2NH3(conc)

    [Ag(NH3)2]+

    (aq) + Br

    (aq)

    I(aq)

    Iodide

    Pale yel lowppt.AgI

    remains insoluble(No further change to the pale

    yellow ppt.)

    remains insoluble

    (No further change to the paleyellow ppt.)

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    Silver nitrate solution

    AgNO3(aq) is used to test for the presence ofhalide ions in solution.

    Anion ppt. Addition of Ammonia NH3

    Colour formula dilute concentrated

    Chloride ; Cl

    White AgCl dissolves to givecolourless solution

    dissolves to givecolourless solution

    Bromide ; Br Cream AgBr Slightly soluble

    dissolves to give

    colourless solution

    Iodide ; I Yellow AgI insoluble Insoluble

    AgCl ppt. dissolves in bothdilute and conc. ammonia forming a colourless solution of

    diammine silver(I)ion complex.

    AgCl + 2NH3(aq) Ag(NH3)2+(aq) + Cl(aq)

    White ppt. colourless solution

    Why the solution of the halide sample is kept acidicwith nitric acid HNO3 during

    the precipitation?

    The nitric acid reacts with, and removes, other ions that might also give a white

    precipitate with silver nitrate e.g Ag2CO3.

    Ag2CO3(s) + 2HNO3(aq) 2AgNO3(aq) + H2O(liq) + CO2(g)

    AgX with sunlight Photodecomposition

    F Cl Br I

    Silver halide AgF AgCl AgBr AgI

    Effect ofsunlight onsilver halide

    No effect whitegreythe ppt. darkens

    creamyellow/greenthe ppt. darkens

    remains yellow

    To eliminate possible interference from anions (e.g CO3

    ) that can also

    form insoluble silver salts.

    Ag(aq) + X

    (aq) AgX(s)

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    Act ion of co ncentrated s ul fur ic ac idon hal ide salts :

    Halide salts react with conc. H2SO4 to give steamy fumes hydrogen halide HX(g) in

    moist air & hydrogen sulfate (or sulfate).

    The reaction is hazardous & must carried on small scale and in a fume cupboard.

    Steamy white fumes

    Conc. H2SO4 displaces hydrogen chloride from sodium chloride:

    NaCl(s) + H2SO4(liq) NaHSO4(s) + HCl(g)Steamy white fumes

    HBr can be displaced from KBr :KBr(s) + H2SO4(liq) KHSO4(s) + HBr(g)

    Steamy white fumesbut some of the HBr is oxidised by conc. H2SO4

    2HBr(g) + H2SO4(l) Br2(g) + 2H2O + SO2(g) oxidation of HBr

    -1 +6 0 +4Brown fumes

    SO2(g) is a colouless gas it cant be seen!SO2(g) turns a filterpaper soaked with acidified K2Cr2O7from orangeto green.

    HI can be displaced from KI :KI(s) + H2SO4(liq) KHSO4(s) + HI(g)

    Steamy white fumesConc. sulfuric acid also oxidises HI but the reaction goes further as HI is a better reducing agent.

    Hydrogen sulfide has a rotten egg smell.

    8HI(g) + H2SO4(l) 4I2(s/g) + H2S(g) + 4H2O(l) oxidation of HI

    -1 +6 0 2

    NaX(s) + H2SO4(liq) NaHSO4(s) + HX(g)

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    Conc.

    H2SO4

    Halide Observation on Adding Conc. H2SO4 reaction products

    Chloride ; Cl white steamy fumes in cold HCl(g)Blue damp litmus turns red

    Bromide ; Br white steamy fumes in cold Brown ororange fumes

    HBr(g)Br2(g)

    Iodide ; I

    white steamy fumes in cold purple fumes black solid (on test tube walls) yellow solid Bad egg smell

    HI(g)I2(g)I2(s)S8(s) or S(s)H2S(g)

    Simple chemical tests for the Halogens X2

    Element Colourin waterColour in hydrocarbon

    solvent(e.g hexane) orVolasil

    chlorine Paleyellow pale yellowishgreen

    Bromine Yellow (brown) RedOrange

    Iodine brown purple

    Chlorine Cl2turns blue litmusred then bleaches it. Cl2 displaces bromine and iodine from bromide or iodide solutions.

    Cl2(aq) + 2NaBr(aq) 2NaCl(aq) + Br2(aq)

    Cl2(aq) + 2KI(aq) 2KCl(aq) + I2(aq)

    Bromine displaces iodine from an iodide solution.

    Br2(aq) + 2KI(aq) 2KBr(aq) + I2(aq)

    Iodine turns starch blue black.

    HCl(g) white fumes

    HBr(g) white fumes ; SO2(g) ; Br2 (g) orange fumes ;

    HI(g) white fumes ; H2S(g) smell ofbad eggs ;

    I2 (g/s) purple fumes & grey solid ; S8 yellow solid

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    Flame colou rs

    Metal

    ion

    Lithium

    Li+

    Sodium

    Na+

    Potassium

    K+

    Magnesium

    Mg2+

    Calcium

    Ca2+

    Strontium

    Sr2+

    Barium

    Ba2+

    Flame

    colourRed Yellow

    persistent

    Lilac Colourless

    No colour (Brick)Red CrimsonRed

    green

    How you can carry out a flame test?

    1. Take 45 drops ofconc. HClon a watch glass.[chlorides salts are very volatile than others].

    2. Make the Nichrome wire red hot and dip it into the acid and then heat

    again until there is no colour is seen when the wire is in the flame.[

    3. Moisten the head of the Nichrome wire with the conc. HClacid

    4. Dip in the sample and then place it in the hottest roaring part of the flame.

    5. Observe the flame. Repeat the steps if necessary.

    Reasons for us ing Nichrom e wire:

    chemically Unreactive

    stableathigh temperaturesin air and with HCl acid

    does not colour the flame.

    1. Calcium compounds produce yellow red (brick-red) flame butmagnes iumcompounds do no t. Explain the difference.

    2. A flame test formore than ONE cation is not reliable or possible ( e.g Na+ and Ba2+).Explain why.

    The difference in energyE = h c/ between the exited energy level and theground state is NOT within the visible spectrum for Mg2+ ions.

    since ONE flame hidesor obscures the other flame (e.gyellow is longerlasting

    than the apple green colour.

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    Thermal decoposi t ion

    Thermal Stability of Group I & II Nitrates NO3&Carbonates( CO32

    ) :

    Group II nitrates M(NO3)2 decompose on heating to produce a metal oxide

    (MO), a brown nitrogen dioxide NO2 gas and

    oxygen gas.

    Ba(NO3)2 >> Sr(NO3)2 > Ca(NO3)2 > Mg(NO3)2 >>Be(NO3)2

    2 Mg(NO3)2(s) 2MgO(s) + 4 NO2(g) + O2(g)Magnesium nitrate magnesium oxide brown gas

    Group I nitrates MNO3 [ other than Li]:All decompose on heating, except LiNO3 ,to produce a metal

    nitrite MNO2, and oxygen gas.

    KNO3(s) heat KNO2(s) + O2(g)potassium nitrate potassium nitrte

    Exception ( with lithium nitrate)

    4 LiNO3(s) heat 2Li2O(s) + 4 NO2(g) + O2(g)lithium nitrate lithium oxide nitrogen dioxide

    (acidicbrown gas)

    Above 70 C, sodium bicarbonate decomposes into sodium carbonate,

    waterand carbon dioxide.

    2 NaHCO3 heat Na2CO3 + H2O + CO2

    M(NO3)2(s) MO(s) + 2NO2(g) + O2(g)

    MNO3(s) heat MNO2 + O2(g)

    ExceptLiNO3

    http://en.wikipedia.org/wiki/Sodium_carbonatehttp://en.wikipedia.org/wiki/Waterhttp://en.wikipedia.org/wiki/Waterhttp://en.wikipedia.org/wiki/Sodium_carbonate
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    Group II carbonates ( MCO3 ) They decompose on heating to produce a metaloxide (MO and CO2)

    at room temperature BeCO3(s) BeO(s) + CO2(g)

    at 540oC MgCO3(s) MgO(s) + CO2(g)

    at 1360oC BaCO3(s) BaO(s) + CO2(g)

    BaCO3 SrCO3 CaCO3 MgCO3 BeCO3

    Note: Both nitrates M(NO3)2(s) and carbonates MCO3(s) become more

    thermally stable down the Group

    Carbonates of Group 1; M2CO3

    Group I carbonates M2CO3 do not decompose at normal Bunsen

    burner temperature except Li2CO3

    Li2CO3(s) heat Li2O(s) + CO2(g)

    Na2CO3 does not decompose at all but it melts at 850oC.

    MCO3 s MO s + CO2

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    Investigating the trend (ease) in the thermal stability of thecarbonate MCO3 of the elements of group 2

    The rate of CO2(g) gas production is slower down the group soThe carbonates become more thermally stable down a group.

    Amount of metal

    carbonate MCO3used / moles

    Mass of metal carbonate

    MCO3 used / g

    m = n Mr

    Volume ofCO2

    gas produced after

    2 minutes / cm3

    MgCO3 2.5103

    2.5103

    84 = 0.21g

    CaCO3 2.5103 2.5103 100 = 0.25g

    SrCO3 2.5103

    2.5103

    147.6 = 0.37g

    BaCO3 2.5103

    2.5103

    197 = 0.50g

    Heat

    D

    ecreasing

    volume

    100 cm graduatedsyringe

    Use the same number ofmoles ofmetal carbonate MCO3

    Heat each carbonate separatelyin a test tube in an identical manner.

    Keep the test tube at the same height (or same position)

    Keep Bunsen in the same position,

    Use the same flame strength i.e always use roaring flame.

    Measure & record the volume of CO2(g) collected in the gas syringeafter2 minutes(same time).

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    QuestionA student investigated the ease with which Group 2 metal carbonates thermally

    decompose when heated with a Bunsen burner.

    XCO3(s) XO(s) + CO2(g)

    (a) Each test tube must be heated directly by a Bunsen flame in an identical manner.

    Suggest how this can best be achieved.

    (b) In each experiment, the student used the same number of moles of metal

    carbonate.

    The mass of magnesium carbonate, MgCO3, heated was 0.21 g.

    Calculate the mass of barium carbonate, BaCO3, that should be used for a valid

    comparison.

    (c) The following results were obtained after heating each sample for two minutes.

    Metal carbonate in

    the test tube

    Volume of gas

    produced/ cm3

    None 9

    MgCO3 20

    CaCO3 13

    SrCO3 11

    BaCO3 9

    (i) Why was a test tube containing no metal carbonate heated? (1)

    (ii) Use the results in the table to describe the trend in thermal stability of the Group 2metal carbonates. (2)

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    Reactions of acids

    1. acids with metal carbonates

    CaCO3(s) + 2HCl(aq) CaCl2 + H2O + CO2(g)

    CaCO3(s) + 2CH3COOH(aq) Ca(CH3COO)2 + H2O + CO2(g)

    Na2CO3 + 2HCO2H(aq) 2NaHCOO

    + H2O + CO2(g)

    Ionic Equation

    2. acids with metal hydrogencarbonates

    KHCO3(s) + HCl(aq) KCl + H2O + CO2(g)

    Ionic Equation

    3. acids with metal oxides

    CaO(s) + 2HCl(aq) CaCl2 + H2O

    White solid colourless solution

    CuO(s) + 2HNO3(aq) Cu(NO3)2 + H2OBlack solid blue solution

    Metal carbonate + acid salt + water+ carbon dioxide

    CO32(aq) + 2H

    +(aq) H2O + CO2(g)

    Metal oxide + acid salt + water

    Metal hydrogencarbonate + acid salt + water + carbon dioxide

    HCO3(aq) + H+(aq) H2O + CO2(g)

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    4. acids with metals (above H)

    [ Mg ; Zn . . . etc.]

    Mg(s) + 2HCl(aq) MgCl2 + H2(g)

    Zn(s) + H2SO4(aq) ZnSO4 + H2(g)

    Ionic Equation

    5. acids with sulfite salts

    Ionic Equation

    BaSO3(s) + 2HCl(aq) BaCl2(aq) + H2O + SO2(g)

    Summary of Act ion of di lute acids

    Action ofacid LIKELY CAUSE

    Inference

    CO2 gas evolved Carbonates orhydrogencarbonates of metalsother than Group 1*

    CaCO3 heat CaO + CO2(g)

    NH3 Ammonium salts

    Sulfur dioxide SO2 evolved on warming Sulfite

    SO32(aq) + 2H (aq) heat H2O + SO2

    Sulfur dioxide SO2

    and pale yellow ppt.

    formed thiosulphate

    Hydrogen A metal ( above Hydrogen) e.g Zn, Mg, Fe..

    Nitrogen dioxide NO2 evolved2NO2

    + 2H

    + H2O + NO(g) + NO2(g)

    nitrite

    M(s) + 2H+(aq) M2+ (aq) + H2 (g)

    SO32

    +

    2H

    +

    (aq)heat

    H2O + SO2(g)

    Metal + acid salt + hydrogen

    Sulfite salt + acid salt + water + sulfur dioxide

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    * To distinguish between carbonate & hydrogencarbonate HCO3

    TEST OBSERVATIONS

    Carbonate Hydrogencarbonate

    on aqueous solution CO3

    HCO3

    pH 12 14 8 9

    boil No changeCO2 evolved &

    pH increases to 1214

    Add aqueous solution of

    MgSO4 or Ca2+

    (aq)

    Immediate ppt. at room

    temp.

    No ppt. at room temp.

    A white ppt. only forms on

    boiling.

    Sodium hydroxide solution

    Observation on adding

    NaOH(aq)

    Observation on adding

    EXCESS NaOH(aq) Likely ions

    White ppt.

    ppt. dissolves to give a

    colouless solution

    Pb2+ ; Zn2+ ; Al3+

    Whiteppt. ppt. is insoluble Mg2+ ; Ca2+ ; Sr2+

    No ppt. Na+

    ; K+

    ;

    No ppt. but NH3evolved

    NH4+

    NH4+

    (aq) + OH

    (aq) NH3(g) + H2O(l)

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    Q u e s t i o n s

    1. Complete the table below.

    Observation expected for a

    positive resultReagents or testGas

    Glowing splintOxygen

    Carbon dioxide

    Solution turns from

    . . . . . . . . . . .to . . . . . . . . . . . . .

    Potassium dichromate(VI)

    solution acidified withdilute sulfuric acid

    Sulfur dioxide

    Turns red and is thenbleached white

    Moist blue litmus paper

    2. Salt D contains one cation and one anion.

    Complete the table, giving tests and observations to show that ammonium ions,NH4+, is

    present in D.

    Test Observation Inference

    NH4+, ions

    (ii) Complete the inference statements in the table below.

    Test Observation Inference

    Aqueous barium chloride isadded to a solution ofD.

    Dilute hydrochloric acid isthen added.

    White precipitate isformed which does

    not dissolve in dilutehydrochloric acid.

    The precipitate is

    ........................................

    Therefore the anion in D is

    ........................................

    (2)

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    3. A series of tests was carried out on a white solid X.

    In the tables below complete the inferences.

    (a) A flame test was carried out on X.

    InferenceObservation

    The metal ion is.........................................The colour of the flame was green

    (b) Dilute sulfuric acid was added to an aqueous solution ofX.

    InferenceObservation

    The precipitate is ....................................................White precipitate

    (c) X was heated, very strongly.

    InferenceObservation

    The gas is ................................................................A brown gas was evolved.

    (d) A sample ofX was warmed with aqueous sodium hydroxide and aluminium powder.

    InferenceObservation

    The gas is ...............................................................

    The anion in X is ....................................................

    A gas was evolved which turned

    red litmus blue.

    (e) The formula ofX is ...........................................................................

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    4. A student was given three aqueous solutions P, Q, and R. Complete the

    test and observations which lead to the conclusions.

    test Observation conclusion

    (a) To a few cm3 ofP, dilutenitric acid and aqueousbarium nitrate were added.

    P contains SO42

    (b) To a few cm3 ofQ dilute

    hydrochloric acid wasadded.

    The gas given off wastested.

    Q contains CO32

    ions

    (c) yellow precipitate R containsI

    Iodide ions.

    5. Describe tests you would use to distinguish between the following pairs ofcompounds.Include the results you would expect foreach compound.

    (a) Sodium nitrate, NaNO3, and ammonium nitrate, NH4NO3.

    (b) Sodium carbonate, Na2CO3, and sodium hydrogencarbonate, NaHCO3.

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    6. For each compound in the pair, describe the observations you would expect to makewhen the test is carried out. If a gas is evolved, include the name of the gas.

    (a) Solid sodium chloride and solid potassium chloride.

    Test: Flame test.

    Observation with sodium chloride: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    Observation with potassium chloride: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    (b) Aqueous potassium sulfate and aqueous potassium sulfite.

    Test: Addition of dilute hydrochloric acid followed by aqueous

    barium chloride.

    Observation with potassium sulfate: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    Observation with potassium sulfite: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    (c) Solid ammonium sulfate and solid potassium sulfate.

    Test: Warm with aqueous sodium hydroxide, testing any gas

    with damp red litmus paper.

    Observation with ammonium sulfate : . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    Observation with potassium sulfate: : . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

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    (d) Solid sodium chloride and solid sodium bromide.

    Test: Add concentrated sulfuric acid, testing any gas evolved

    with damp blue litmus paper.

    Observation with sodium chloride: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    Observation with sodium bromide: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

    7. The tables below show a series of simple tests on different compounds. Fill in the spaces

    in the tables.

    Test Observation Inference

    The flame test was carried

    out on solid A.Potassium ions present in A.

    Test Observation Inference

    To an aqueous solution of

    B,add . . . . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . . .

    followed by. . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . . .

    A yellow precipitate was

    produced that wasinsoluble in concentrated

    ammoniasolution.

    Iodide ions present in B.

    Test Observation Inference

    Add dilute hydrochloricacid to solid C. Heat the

    mixture and pass the gas

    through acidified potassium

    dichromate(VI) solution.

    Orange solution goes

    green.

    Gas evolved . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . .

    Anion in C . . . . . . . . . . . . .

    . . . . . . . . . . . . . . . . . . . .