5.3.2 Complexes, Ligands, Colour Changes and Entropy PDF
5.3.2 Complexes, Ligands, Colour Changes and Entropy PDF
5.3.2 Complexes, Ligands, Colour Changes and Entropy PDF
(a) Hydrated nickel(II) salts are green in colour. Give the electron configuration of a
nickel(II) ion and hence state why the ion is coloured.
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(2)
(b) (i) Which is the only nickel compound, in Table 5.3 in the Book of Data, in which the
nickel atom does not have an oxidation number of +2?
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(1)
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(1)
(c) Nickel(II) chloride solution contains the ion Ni(H2O)62+(aq). On adding ammonia
solution, the colour changes to blue or purple as different complexes are formed.
(i) Write the equation, including state symbols, for the displacement of one water
molecule by an ammonia molecule.
(1)
(ii) Would you expect ΔSsystem for this reaction to be positive, negative or close to
zero? Justify your answer.
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(2)
(d) The complexes formed when ammonia solution is added to nickel(II) chloride solution
have the formula [Ni(H2O)x(NH3)6–x]Cl2. An experiment was carried out to determine the
value of x in one of them.
A sample of 5.000 g of this complex was dissolved in water and reacted with excess
silver nitrate. 6.133 g of silver chloride was produced.
(i) Write the ionic equation, including state symbols, for the formation of silver
chloride.
(1)
Each mole of the complex contains two moles of chloride ions. Calculate the
number of moles of the complex present in the 5.000 g sample.
(3)
(iii) Use your answer in (ii) to calculate the value of x and hence the formula of this
complex ion.
(1)
(2)
(Total 14 marks)
(a) (i) State the full electronic configuration of a chromium atom in the ground state,
using the s,p,d notation.
(1)
(ii) Apart from differing numbers of electrons, how does the ground state electronic
configuration of chromium differ from those of the two adjacent elements in the
Periodic Table, vanadium and manganese? Suggest the reason for this difference.
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(2)
(b) Compounds containing the chromium(II) ion, Cr2+, are unstable in aqueous solution
because they are readily oxidised by oxygen in the air.
State the appropriate electrode potentials and half-cells, and use them to explain why this
oxidation takes place.
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(3)
(c) A useful method of stabilising an unstable oxidation state is to form a complex. You may
have prepared chromium(II) ethanoate, Cr2(CH3CO2)4(H2O)2, where the Cr2+ ion is
stabilised in this way. [Details can be found on pages 464–465 of your Students’ Book.]
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(2)
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(1)
(iii) Deduce the number of hydrogen peaks in the NMR spectrum of the complex from
the structural formula Cr2(CH3CO2)4(H2O)2. Justify your answer.
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(2)
(iv) Suggest TWO characteristic absorptions in the infra-red spectrum of the complex.
You should state the bond associated with each absorption and give the
corresponding absorption value in wavenumbers.
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(2)
(d) (i) When first introduced, breathalysers used acidified sodium dichromate(VI) crystals
to detect ethanol on the breath. Using oxidation numbers, or otherwise, balance the
equation for the reaction.
(2)
(ii) State the colour change you would expect to see if exhaled air containing an
excessive amount of ethanol reacted with the breathalyser chemicals.
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(1)
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(1)
(Total 17 marks)
3. The element iodine can be produced from the mineral Chile saltpetre, which contains sodium
iodate, NaIO3. The iodate ions are converted to iodine in a two-step process.
(a) (i) Describe a test you could carry out to confirm the presence of iodide ions in a
solution. Indicate the result of the test.
Test ...................................................................................................................
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Result ................................................................................................................
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(2)
(ii) Identify the TWO elements in Step 1 which show a change of oxidation number
during the reaction.
(iii) The equation for Step 1 shows that 1 mole of iodate ions, IO3–, reacts with 3 moles
of hydrogensulphite ions, HSO3. Show that your answers to (ii) agree with this
ratio.
(1)
(b) An experiment was carried out to determine the concentration of the iodine prepared in
Step 2
A 10.0 cm3 portion of the iodine solution was titrated with sodium thiosulphate solution
of concentration 0.0100 mol dm–3. The volume of sodium thiosulphate solution added at
the end-point was 24.0 cm3.
(i) What piece of apparatus would you use to measure out the 10.0 cm3 portion?
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(1)
(ii) Suggest a suitable indicator to show the end-point of this titration. State the colour
change you would see.
Indicator .................................................................................................................
(iii) Calculate the number of moles of sodium thiosulphate used in the titration.
(1)
(iv) Calculate the number of moles of iodine which reacted with the sodium
thiosulphate solution.
(1)
(1)
(Total 12 marks)
4. Air is drawn through 10.0 cm3 of an aqueous solution of vanadium(II) chloride of concentration
0.100 mol dm–3. The colour of the solution slowly changes as oxidation takes place.
(i) Draw a diagram of suitable apparatus for carrying out the air-oxidation of the
vanadium(II) chloride solution.
(1)
(ii) Complete the half equation for acidified manganate(VII) ions acting as an oxidising
agent.
(iii) Calculate the number of moles of manganate(VII) ions used in the titration, and hence the
number of moles of electrons removed by the manganate(VII) ions.
Calculate the number of moles of vanadium(II) ions in the 10 cm3 of solution used. Find
the oxidation number of vanadium in the air-oxidised solution given that vanadium(V)
ions are formed in the titration.
(4)
(iv) Suggest ONE reason why acidified potassium manganate(VII) is a useful oxidising agent
in redox titrations.
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(1)
(Total 7 marks)
5. Brass is a widely-used alloy that contains copper and zinc. There are many varieties of brass
with different compositions.
In the volumetric analysis of the composition of brass, the first step is to react a weighed sample
of the alloy with nitric acid. This gives a greenish-blue solution.
(a) The following standard electrode potentials are needed for this question:
Eο/V
Zn2+ + 2e– Zn – 0.76
Cu2+ + 2e– Cu + 0.34
NO3– + 2H+ + e– NO2 + H2O + 0.81
(i) Use the half equations given above and the values of Eο to calculate the standard
electrode potential for the reaction between zinc and nitric acid and derive the
equation.
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(2)
(ii) Suggest why zinc does not produce hydrogen with nitric acid.
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(2)
(iii) If the greenish-blue solution is diluted with water it turns light blue and contains
hydrated copper(II) ions.
Name the light blue complex ion and draw its structure so as to show its shape.
Name .................................................................................................................
Structure:
(2)
(iv) If concentrated hydrochloric acid is added to a portion of the light blue solution it
turns green.
State the type of reaction that occurs and give an equation for the reaction.
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(2)
(b) The light blue solution from (a)(iii) is then neutralised, and reacted with an excess of
potassium iodide solution.
Eο/V
2+ – +
Cu + e Cu + 0.15
I2 + 2e– 2I– + 0.54
(i) Use these Eο values to explain why you would not expect the following reaction to
occur.
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(1)
(ii) Explain why, in practice, the reaction in (i) does occur and iodine is liberated.
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(2)
(iii) When the precipitate formed in the reaction in (i) is filtered off and then dissolved
in concentrated aqueous ammonia, a colourless solution is produced.
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(1)
(iv) If the colourless solution from (iii) is left to stand in air for some time, it turns blue.
State why this is so, naming the reactant responsible for the change.
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(2)
(c) In a determination of the composition of a sample of brass, 1.50 g of the alloy was treated
to give 250 cm3 of a neutral solution of copper(II) nitrate and zinc nitrate.
Excess potassium iodide solution was added to 25.0 cm3 portions of this solution, and the
liberated iodine titrated with 0.100 mol dm–3 sodium thiosulphate solution. The mean titre
was 16.55 cm3.
(i) State which indicator you would use for the titration and the colour change seen at
the end point.
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(2)
(ii) Explain why the indicator is not added until the reaction is nearly complete.
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(1)
(5)
(Total 22 marks)
Cu : [Ar] ......................................................................................................................
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(2)
(ii) Copper(I) ions disproportionate in aqueous solution. Give the equation for the
reaction and use the standard electrode potentials given below to explain why the
reaction occurs.
Eο/V
Cu2+(aq) + e– Cu+(aq) + 0.15
Cu+(aq) + e– Cu(s) + 0.52
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(2)
(iii) Explain why your answer to (ii) does not rule out the existence of Cu+(aq) under
standard conditions.
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(1)
(c) (i) When a small amount of dilute ammonia solution is added to a solution of
copper(II) sulphate, a turquoise blue precipitate, F, is formed.
(2)
(ii) When F is dissolved in dilute hydrochloric acid, the resulting blue solution gives a
white precipitate with barium chloride solution.
Suggest a formula for F, given that all the hydrogen is present in hydroxide ions.
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(2)
(iii) When excess concentrated ammonia is added to F, a deep blue solution is formed.
Give the formula of the ion responsible for this colour.
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(1)
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(1)
(d) Copper metal can be used as a catalyst. When propan-1-ol vapour is passed over heated
copper, the following reaction occurs:
CH3CH2CH2OH → CH3CH2CHO + H2
(i) Outline how, by the use of 2,4-dinitrophenylhydrazine and suitable tables of data,
you could show that the product is propanal.
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(4)
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(1)
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(1)
(iv) Suggest why the oxidation of the alcohol by passing it over heated copper does not
lead to further oxidation of the aldehyde.
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(1)
(v) There are a few places on the surface of the metal where catalysis can occur.
These are called ‘active sites’.
Suggest why this leads to the rate of reaction being independent of the gas pressure
unless this pressure is extremely low.
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(1)
(Total 20 marks)
Cr: [Ar]…………………………….
Cu: [Ar]……………………………..
(1)
(ii) The electronic configurations of chromium and of copper are not readily
predictable from a consideration of the elements on either side of them in the first
transition series in the Periodic Table.
State how these electronic configurations differ from others in the first transition
series and explain why this difference arises.
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(2)
(i) Draw the structure of this ion so as to clearly show its shape.
(1)
(ii) How are the bonds between the water ligands and the metal ion formed?
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(1)
(iii) Write an equation to show what happens initially when a solution containing
hydroxide ions is added to a solution of [Cr(H2O)6]3+ ions.
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(2)
(iv) State what you would see as dilute sodium hydroxide is gradually added to a
solution of [Cr(H2O)6]3+ until it is in excess.
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(2)
(v) What property of chromium(III) hydroxide is shown by the reaction in part (iv)?
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(1)
(c) (i) A 1.00 g sample of a metal alloy that contains chromium was converted into
250 cm3 of an acidified solution of potassium dichromate(VI).
25.0 cm3 of this solution was added to an excess of potassium iodide solution.
The iodine liberated was titrated with 0.100 mol dm–3 sodium thiosulphate
solution.
Calculate the amount (moles) of iodine liberated and hence the percentage, by
mass, of chromium in the alloy.
(5)
(ii) In titrations involving iodine, starch is usually added near the end-point to make the
colour change clearer, although in many cases it is not really necessary.
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(1)
(Total 16 marks)
8. Methanol can be vigorously oxidised with an acidified solution containing dichromate(VI) ions,
Cr2O72–, to form methanoic acid and chromic(III) ions.
(a) What are the oxidation numbers of carbon in methanol and methanoic acid?
A –1 +1
B –2 +2
C +1 –1
D +2 –2
(1)
(b) How many moles of methanol react with one mole of dichromate(VI) ion, Cr2O72–?
A 1
B ¾
C 1½
D 3
(1)
(Total 2 marks)
9. Which of the following will not act as a ligand in the formation of complexes?
A C6H5NH2
B CH3NH2
C NH4+
D NH3
(Total 1 mark)
10. Which of the following ground state electron configurations corresponds to an element most
likely to form an oxide with catalytic properties?
A 1s2 2s2
11. Which chemical term best describes what happens, when butylamine is added to a solution of a
copper(II) salt?
A precipitation
B redox
C proton transfer
D complex formation
(Total 1 mark)
Fe [Ar] .........................................................................................................
(ii) Draw the structure of the hexaaquairon(II) ion, [Fe(H2O)6]2+, clearly showing its
shape.
(1)
(iii) Give the equation for the complete reaction of hydroxide ions with a solution of
hexaaquairon(II) ions.
(1)
(iv) State what you would see if the product mixture in (iii) is left to stand in air.
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(1)
(i) Define the term standard electrode potential with reference to this electrode.
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(3)
(ii) Explain why the value of Eο suggests that the iron will react with an aqueous
solution of an acid to give Fe2+ ions and hydrogen gas.
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(2)
(iii) State why Eο values cannot predict that a reaction will occur, only that it is
possible.
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(1)
(Total 10 marks)