Faiz Ul Hassan (Al-Chemist)
Faiz Ul Hassan (Al-Chemist)
Sources cie endorsed books, website and past papers and Al—Chemist Faiz Ul Hassan
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*The remaining 12 marks will be allocated across the skills in this grid, and their allocation may vary from
session to session.
Tip You should read a burette to the nearest 0.05 cm3, in other words halfway
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between two of the smallest divisions. You cannot estimate more precisely than this because the smallest
drop a burette can deliver is approximately 0.05 cm3. A common mistake students make is in calculating the
average burette reading used in a titration. This cannot have a greater degree of accuracy than the burette can
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produce. Therefore, the average burette reading has to end in .00 cm3 or .05 cm3 Anything else is wrong and
will be penalised.
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In a titration you need to carry out sufficient repeat titres to establish the ‘correct’ end point. For a titration
with a sharp end point this should be within 0.10 cm3.
Tip Once you have established the approximate end point, say 22.60 cm3, for the accurate titrations, you can
run in 20 cm3, swirling the mixture, before adding a few drops at a time. This will save time. It is important
that you always try to pick the same point for determining the end point. If it is a potassium manganate(VII)
titration this is when the mixture just has a permanent pale pink colour. If it is an acid–base titration, the end
point is when the indicator just remains in its acid state on swirling.
Tip Do not add more than two or three drops of indicator unless instructed otherwise. Using more indicator
does not give a more precise end point because all of the indicator has to change to its acid form.
If you are asked to perform a kinetics experiment, read carefully through the instructions before you start.
Make sure that you have everything ready before you start the reaction -reagents measured out, stopwatch
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ready, thermometer in place (if relevant). Being organised is the best way to get good results and to avoid
wasting time.
Tip In a kinetics experiment, if you are adding a quantity of one reagent to another, make sure that you start
the stopwatch at the same point each time. This could be halfway through adding the reagent, or at the point
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of the whole mixture (this is particularly important if the mixture contains a solid). Get ready by checking
the position of the mercury in the thermometer as you are coming up to the next timed reading.
Observations
In most examinations one specific question involves making careful observations, recording them and then
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drawing conclusions from these observations. If you are to score good marks on this question it is vital that
you make good observations and record these accurately.
To make sure your observations are correct you must be certain that you follow the instructions completely.
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happen
●● using too much of the ‘unknown’ or too much reagent — this can mask observations
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●● using a solid ‘unknown’ rather than a solution of the substance —observations may be different or
masked
●● failing to test for a gas produced (lighted splint, glowing splint, indicator paper, smell) — marks will be
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in. In other exercises, such as titrations, you may need to draw your own table for the data.
You may also be asked to draw a graph to display the results of an experiment. Here are some tips on what
is needed to score high marks when drawing a graph.
Tip There are a number of key features on a graph that examiners look for:
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●● the independent variable plotted on the x-axis and the dependent variable on the y-axis
●● use of a sharp pencil for plotting the points and sketching the graph
●● a sensible scale chosen to make the most of the graph paper (at least half in both dimensions)
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The diagram below shows how to draw a ‘line of best fit’. The line is placed so that points are equidistant
from the line with equal numbers of points on each side.
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The diagram below shows what is meant by an ‘outlier’ — a result which, for some reason, is clearly not
part of the data set we want to use.
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When an experiment produces qualitative data, it is just as important to represent the data accurately.
Accurate recording of what happened at different stages of an experiment — for example when a few drops
of reagent were added, when more reagent was added and when the reagent was present in an excess — will
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help you
explain what is happening and score the available marks.
Try to use accurate and unambiguous language when describing colours or colour changes. Make sure that it
is clear whether you are referring to a solution or a precipitate in the solution.
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Tip The words you use must be clear to the examiner as well as to yourself.
●● Do not use words such as ‘see-through’ or ‘transparent’ when you mean ‘colourless’. It is perfectly
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possible to ‘see through’ potassium chromate(VI) solution but it is not colourless, and copper(II) sulfate
solution is ‘transparent’, but it is not colourless.
●● Try to be as precise as possible about colours. A simple word like ‘blue’ is rarely enough to describe
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colour changes such as those that take place when aqueous ammonia is progressively added to a solution of
copper(II) ions.
●● If a gas is given off remember that the observation is that ‘bubbles are produced’ or ‘effervescence takes
place’, not just that ‘carbon dioxide is evolved’. If the gas is carbon dioxide you also need to say how you
tested for it — for example ‘it turned limewater milky/cloudy’.
In order to draw conclusions and evaluate the procedures you have carried out, you first need to analyse the
results of any practical you complete, and then explain what they show. Before reaching a conclusion you
may need to carry out a calculation. If this is the case, you should show the key steps in the calculation so
that it can
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be followed by the examiner who can then check the accuracy. For example, in a titration a series of repeats
is undertaken to ensure accuracy and to identify any anomalous results. When the average titre is calculated,
an anomalous result should be excluded from the calculation.
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You may be asked to draw a graph to display results because this is an excellent way to show trends or
relationships. A straight-line graph passing through the origin shows a directly proportional relationship
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between the dependent and independent variables. Sometimes the graph will be a curve and you may need to
measure the gradient of the curve at different points. When doing this, use large triangles to calculate the
gradient as this gives a more accurate calculation. Remember that a graph provides evidence to support a
conclusion.
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Evaluation
This is one of the hardest skills to develop. It relies on your ability to think critically about the reliability of
the data you have collected and the conclusions drawn. One way to do this is to think about the errors that
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Useful Tips
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Don't perform unnecessary titrations, if you did two and got results close to each other then there's no
need for a third one.
Always draw a triangle on the graph to find the gradient, if you are asked to find it.
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Latest salt analysis sections contain a trick with aluminium and lead(II) ions because they have the
same results with ammonia and sodium hydroxide. The test that distinguished them is addition of
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HCL, it will form a precipitate with lead(II) ions but not with aluminum ions. (Lead(II) ions can be
distinguished from aluminium ions by the insolubility of lead(II) chloride.)
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Always heat solutions in a boiling tube and not the test tube.
When you write the observation for some gas that is released, always include a confirmatory test. You
should actually never perform these confirmatory tests (to save time) just use your knowledge of
chemistry to find which gas is released but always include the test in the observations. E.g. when a
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carbonate is reacted with an acid, you should write the observation; "Colorless gas released which
turns lime water milky."
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Remember some gases are hard to see when released in a test tube, so where you expect some gases
to be released, look carefully for the observation. A good idea is to use the white tile or if you're not
provided with it then use your paper as the background when looking at the test tube.
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In the exam if you think some solution has some impurity or you put something into it by mistake then
just ask them to replace it, don't use it.
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Remember to not to use the same dropper for two different solutions.
If some solution involves heating and then heating strongly then you really need to heat it strongly so
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Always wash the thermometer before using, and make sure its working before using, when not dipped
into any solution, it should give a constant reading of 25-30 °C.
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Try to work in a clean and objective oriented environment, what I mean is when you're working with
1 part of the paper then just keep the solutions needed for that part to yourself and keep the others
away. This helps a lot.
Always draw tables(similar to how they give you in the questions) to represent results and
observations, don't just write them down in lines.
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1. acid-alkali titration
2. enthalpy change
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- don’t push the thermometer through the base of the cup
- record temperature to 1 decimal place
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ANALYSING
Don’t forget:
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Make sure you only include concordant titrations in your average titre value
b) enthalpy changes
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(in neutralisation reactions the mass of acid and alkali solutions must be added together)
c = 4.18
If the numbers of moles of the two reactants are different, use the smaller number of moles (ie
the reactant not in excess)
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EVALUATING
4. Suggest how the accuracy of the experiment could be improved and explain how the change
would improve accuracy.
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using a wet weighing bottle (this means that the mass used is less accurately known)
Not using the correct apparatus (this means that the quantity is not being measured
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accurately enough)
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- In an enthalpy change, the biggest error is always heat loss. It can be minised by better
lagging or by using a lid.
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- Look at the percentage errors for the apparatus used. For the apparatus giving the
largest error, suggest a way to make that measurement larger, such as
Using more concentrated solutions
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3. enthalpy of combustion
9 Faiz Ul Hassan Khan (Al-Chemist) )0321-9070007
Resource Pack By Faiz Paper 3 Practice Notes Al-Chemist
4. enthalpy of solution/displacement/neutralisation
7. titration
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Use 3 – 5 g of solid
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Apparatus – 2dp balance, crucible, Bunsen burner, tripod, clay pipe triangle
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Weigh crucible (m1), add sensible mass and weigh crucible again (m2)
Repeat experiment
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Compound may be toxic – wear gloves, wash affected areas after spillage
Use PV = nRT to calculate the moles of gas, and hence moles and mass of reactant
Weigh out reactants, add them to flask, and replace bung quickly
For mole ratio – wait until reaction is complete and record volume of gas
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Repeat experiment
or mole ratio:
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Compare ratio
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Eye protection
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4. Place the alcohol burner on top of an accurate balance and record the mass, including lid
5. Place screens on either side of the burner to protect it from wind and heat loss
6. Light the alcohol burner
7. Put out the alcohol burner by placing the lid onto it when 2 grams (eg) have been used
Eye protection
Fuels are toxic/harmful – wear gloves, flood affected areas after spillage
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4. Enthalpy of solution/displacement/neutralisation
2. If enthalpy of solution: use 3 – 5 g (more may not dissolve, less gives large error)
7. Stir mixture
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9. Repeat
Q = mc∆T
Convert to kJ
12 Faiz Ul Hassan Khan (Al-Chemist) )0321-9070007
Resource Pack By Faiz Paper 3 Practice Notes Al-Chemist
Eye protection
Acids/alkalis toxic – use pipette filler, wear gloves, flood affected areas after spillage
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Possible reactions:
- hydrolysis of a haloalkane
- elimination of a haloalkane
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- dehydration of an alcohol
You will be given an outline of the experimental procedure so don’t panic
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Apparatus
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Draw the apparatus to show an alcohol passing over heated ceramic pieces and being
collected over water.
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Make sure your apparatus is never sealed (ie air must be able to escape)
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Reagents Weigh out a few grams of the organic reactant, using a weighing bottle
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1. Work out the reagents that you need, and choose suitable quantities (remember the reagents
are generally in excess)
distils off at the temperature close to the boiling point of the desired product.
Give safety precautions (don’t use flame if anything is flammable, wear gloves, clean spillages
immediately etc)
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6. Qualitative analysis
Although unlikely, you may be asked to plan a simple procedure to identify some simple ions:
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- how silver nitrate, nitric acid and ammonia are used to test for halide ions in solution
- how concentrated sulphuric acid can be used to test for halide ions in solid samples
- that magnesium and calcium ions give a precipitate when a few drops of sodium hydroxide
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- that aldehydes can be identified by their reaction with Felling’s or Tollen’s reagent
- that primary alcohols, secondary alcohols and aldehydes turn acidified potassium dichromate
solution from orange to green
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1. Work out how many moles you need for a sensible titration (25 cm3)
2a. If solid:
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- wash the beaker several times, pouring the washings into the flask
- make up to the mark with distilled water, shaking repeatedly
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2b. If liquid:
-
- release it under gravity into the volumetric flask
- make up to the mark with distilled water, shaking repeatedly
3. wash out the burette with the acid
4. Pour the acid into the burette and take the reading
5. Use a pipette to take a sample of the alkali and release it into a conical flask
Safety issues – eye protection, acids and alkalis are corrosive so wear gloves or flood affected areas
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solution
• Add dilute HCl.
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solution.
• Dissolve the solid in pure White precipitate
water.
Chloride Cl- • Add dilute nitric acid Ag+ (aq) + Cl-(aq) AgCl (s)
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water.
Bromide Br- • Add dilute nitric acid Ag+ (aq) + Br-(aq) AgBr (s)
(removes other ions)
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Chloride I- • Add dilute nitric acid Ag+ (aq) + I-(aq) AgI (s)
(removes other ions)
• Add silver nitrate Insoluble in dil. or conc. ammonia
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2+ excess
Magnesium Mg White precipitate is formed
• or add NaOH(aq) until
excess
• Volumetric analysis:
o Preparing a solution of known concentration (Standard solution):
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Place beaker on balance and weigh between x and y grams of solid (after
checking 0 error).
Make a note of mass added
Add about 100 cm3 of distilled water to beaker and dissolve solid with glass
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rod.
Use a funnel to transfer this to volumetric flask.
Rinse the beaker and glass rod thoroughly with distilled water into the
volumetric flask .
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Add a few drops of indicator into the conical flask. Methyl orange if alkali in flask.
Phenolphthalein if acid in flask.
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Rinse and then fill a burette with acid or alkali up to the 0 mark.
Add the acid or alkali slowly, swirling the flask constantly until indicator turns
(phenolphthalein colourless - pink /methyl orange orange - red)
Stop adding the acid or alkali and record the volume of H2SO4 added.
Repeat the whole experiment until 3 consecutive results within 0.2 cm3 are obtained.
o Errors in titrations:
Percentage error = (actual error / measurement) x 100
Error in pipette = 0.06 cm³
Error in burette = 0.1 cm³
Measurements involving difference: twice the error.
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mass measured.
o Use a measuring cylinder to put 100 cm3 of distilled water into a small beaker and clamps this at a fixed
height above the spirit lamp (about 2 cm).
Record the initial temperature of the water using a thermometer.
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o Light the lamp using a burning splint.
o Heat the water using the spirit lamp until the temperature has gone up by about 10°C. Stir the water
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o Calculate the enthalpy change
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• There may be heat loss due to the apparatus used and heat may have dissipated through the insulating
material should use a polystyrene cup and insulation like a lid.
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• The specific heat capacity and density of water are used (and not of HCl).
• The masses of solid added to the acid are ignored.
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• It is assumed that the specific heat capacity of the polystyrene cup is negligible.
• Some heat is lost when the hydrogen or carbon dioxide are evolved in the reactions.
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• Organic tests:
o Collect 10 cm³ of the samples.
o Test the samples in the following order
Alkenes – bromine water decolourises ?
alkene
Alcohols – Spatula of solid PCl5. Test fumes with damp litmus paper litmus red? White
fumes near ammonia? alcohol
Halogenoalkane – Add NaOH, ethanol as solvent. Shake and warm for 3 minutes. Cool and
add nitric acid + silver nitrate. white = chloride; cream = bromide; yellow = iodide.
Confirm with ammonia
Alkane, the substance left is the alkane.
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• Sulphate solubility
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Hydroxide solubility
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sodium and potassium carbonates no effect (except water of crystallisation may be given off)
lithium and all group 2 nitrates nitrogen dioxide and oxygen evolved
Iodometric Titration
Redox Reaction
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Experiment 1
In this experiment you will determine the ionic manganate(VII) with potassium iodide. Excess potassium iodide
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–3
KMnO4. FA 2 is 1.00 mol dm sulfuric acid, H2SO4.
–3
FA 3 is 0.500 mol dm potassium iodide, KI.
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FA 4 is 0.100 mol dm sodium thiosulfate,
Na2S2O3. starch indicator
(a) Method
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● Pipettecm of25FA.10into a conical flask.
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● Use the measuringcmcylinder ofFA2totheto conicaladd25 flask.
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●
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3
The rough titre is ........................ cm .
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II
III
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IV
VI
VII
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(b) From your accurate titration results, obtain a suitable value for the volume of FA 4 to be used
in your calculations.
Show clearly how you have obtained this value.
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Volume of FA 4 required is ..................... cm . [1]
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(c) Calculations
(i) Calculate the number of moles of sodium thiosulfate in the volume of FA 4 calculated in
(b).
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(ii) Use the equation below to calculate the number of moles of iodine that reacted with the
sodium thiosulfate in the titration.
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(iii) Use information on page 2 to calculate the number of moles of potassium manganate(VII)
in FA 1 used in the titration.
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(iv) From your answers to (ii) and (iii), calculate the number of moles of iodine produced by
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the reaction of 2.00 moles of potassium manganate(VII) with excess potassium iodide.
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(v) Using your answer to (iv), put a tick next to the ionic equation that represents the reaction
between FA 1 and FA 3.
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(vi) Prove that the iodide ion has been oxidised in the equation that you selected in (v).
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[5]
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(d) (i) The error in calibration of the pipette you used is ±0.06 cm .
Calculate the percentage error when measuring FA 1, using the pipette.
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(ii) A student suggested that the experiment would be more accurate if a pipette was used to measure
solution FA 3.
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Dear Students , Do Calculations by using 27.50 cm3 of average titre value( Volume of FA4)
By Al-Chemist .
Rate of Reaction
In this experiment you will investigate how the rate of reaction between sodium thiosulfate
and hydrochloric acid is affected by the concentration of the acid.
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When aqueous thiosulfate ions react with hydrogen ions, H , in any acid, a pale yellow
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precipitate of sulfur is formed. The ionic equation for this reaction is given below.
2– +
S2O3 (aq) + 2H (aq) → S(s) + SO2(aq) + H2O(l)
The rate of the reaction can be determined by me of sulfur.
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–3
FA 4 is 0.10 mol dm sodium thiosulfate,
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–3
Na2S2O3. FA 5 is 0.20 mol dm HCl (aq)
(a) Method
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Experiment 2
● Rinse the larger measuring cylinder, then use it to transfer 40 cm3 of FA 4 into the 100 cm3
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beaker.
● Use the smaller measuring cylinder to add 10 cm3 of distilled water to the beaker.
● Use the same measuring cylinder to add 20 cm3 of FA 5 to the mixture in the beaker and
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10 cm3 of FA 5.
● Measure and record the reaction time to the nearest second.
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(b) (i) The ‘rate of reaction’ can be represented by the formula below.
1000
‘rate of reaction’ = reaction time
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Use this formula to calculate the ‘rate of reaction’ for Experiments 1 and 3. Give the
unit.
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(ii) Calculate the initial concentrations of hydrochloric acid in the reaction mixtures in Experiments 1
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and 3.
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initial concentration of HCl in Experiment 1 = ............................. mol dm
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–3
initial concentration of HCl in Experiment 3 = ............................. mol dm
(iii) How is the ‘rate of reaction’ affected by the concentration of hydrochloric acid in the mixture?
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(iv) Predict how the reaction time measured in Experiment 1 would have been affected if the
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–3 –3
experiment had been carried out using 0.20 mol dm sulfuric acid instead of 0.20 mol dm
hydrochloric acid.
Explain your answer.
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(v) Predict how the reaction time measured in Experiment 3 would have been affected if the
3 3
experiment had been carried out in a 250 cm beaker instead of a 100 cm beaker. Explain your
answer.
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[5][Total: 9]
Dear Students , Consider t1 = 45 s t2 = 49 s t3 = 58 s
Qualitative Analysis
Experiment 1
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At each stage of any test you are to record details of the following.
Where gases are released they described should in the appropriate be identify place in your
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observations.
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Where reagents are selected for use in a test, the name or correct
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Dissolve the FA 6 provided in about 15 cm of distilled water in a boiling
tube. Carry out the following tests and record your observations in the table
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below.
test observations
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hydrochloric acid.
solution of FA 6 in a test-
tube, add an equal volume
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of aqueous hydrogen
peroxide, then
add a few drops of
aqueous barium
chloride or aqueous
test observations
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acid, then
heat the mixture gently and
cautiously.
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(v) Identify the anion in FA 6, and state one piece of evidence for you
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anion ...............................................
evidence ..............................................................................................................................
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(vi) Give the chemical equation for the reaction between FA 6 and hydrogen peroxide, H2O2, in
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[7]
(b) FA 7, FA 8, FA 9 and FA 10 each contain one cation from the list on page.
You will attempt to identify the cations by testing with aqueous sodium hydroxide and
aqueous ammonia.
In each case, use a 1 cm depth of the solution in a test-tube.
observations
test
FA 7 FA 8 FA 9 FA 10
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add
NaOH
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add
aqueous
ammonia
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(ii) Use your observations to identify, as far as possible, the cation present in each
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FA 7 cation ....................................................
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FA 8 cation ....................................................
FA 9 cation ....................................................
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FA 10 cation ..................................................
(iii) Give the ionic equation for the reaction of one of your cations with a few drops of
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(iv) The precipitates obtained when alkalis are added to solutions of certain cations are sometimes
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difficult to see. Suggest how, us could be repeated in a way that would make these precipitates
more visible.
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31 Faiz Ul Hassan Khan (Al-Chemist) )0321-9070007
Resource Pack By Faiz Paper 3 Practice Notes Al-Chemist
[9]
[Total: 16]
ppt
excess no change no change (ppt) insoluble in
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or
2+
• FA 6 with Ba – white precipitate / BaSO3 formed which
dissolves in acid / partially soluble in acid
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(ii) Conclusions
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2+ 2+
• FA 7 – calcium / Ca or barium/Ba
2+
• FA 8 – magnesium / Mg
3+
• FA 9 – aluminium / Al
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2+
• FA 10 – manganese(II)/Mn
3+ –
or M + 3OH → M(OH)3 (for any trivalent cation)
(a) Method
● Pipette 25.0 cm3 of FA 1 into a conical flask.
● Use the measuring cylinder to add 15 cm3 of FA 3, an excess of KI, to the conical flask.
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● Make certain any recorded results show the precision of your practical work.
● Record in a suitable form below, all your burette readings and the volume of FA 2 added in
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[7]
(b) From your accurate titration results, obtain a suitable value to be used in your calculations.
Show clearly how you have obtained this value.
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(c) Calculations
Show your working and appropriate significant figures in each step of your calculations.
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(i) Calculate the number of moles of thiosulfate ions present in the volume of FA 2 you have
calculated in (b).
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(ii) Use your answer to (i), and the equations for the reactions involved, to deduce the number of
moles of Cu2+ present in 25.0 cm3 of FA 1.
2Cu2+(aq) + 4I–(aq) → I2(aq) + 2CuI(s)
2S2O32–(aq) + I2(aq) → S4O62– (aq) + 2I–(aq)
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(iii) Use your answer to (ii) and the mass of CuSO4.xH2O present in the solution, to calculate
the relative molecular mass, Mr, of CuSO4.xH2O.
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Mr of CuSO4.xH2O = .............................
x = .............................
[6]
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Dear Students , Do Calculations by using 23.80 cm3 of average titre value( Volume of FA2)
By Al-Chemist
Finding percentage purity by using water of crystallization
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1 FA 4 is an impure sample of hydrated calcium chloride, CaCl 2.2H2O. On heating, hydrated calcium chloride
loses its water of crystallisation.
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You will determine the purity of FA 4 by measuring the loss in mass that occurs when it is heated.
The impurity present in FA 4 is not decomposed on heating.
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(a) Method
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You should read the instructions carefully before starting any practical work and draw a
table for your results in the space below.
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a further 2 minutes.
● Allow the crucible and its contents to cool. Reweigh the crucible and contents and record
the mass.
● Heat the crucible strongly for a further 2 minutes. Allow it to cool. Reweigh the crucible and
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(b) Calculations
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Show your working and appropriate significant figures in the final answer to each stage of your
calculations.
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heated.
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(iii) Use your results to (i) and (ii) to calculate the percentage purity of FA 4, impure CaCl 2.2H2O.
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Suggest whether this experiment would give a more accurate result for the percentage purity of
FA 4. Explain your answer.
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(d)In your calculations you assumed that the impurity in FA 4 does not decompose on heating.
State how the percentage purity that you calculated in (b)(iii) would change if the impurity were to
decompose on heating.
Explain your answer.
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Dear Students , Do Calculations by using 1.90 g of FA4 and 0.32g lost on heating )
By Al-Chemist
Salt analysis
Qualitative Analysis
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At each stage of any test you are to record details of the following.
● colour changes seen
● the formation of any precipitate
● the solubility of such precipitates in an excess of the reagent added
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Where gases are released they should be identified by a test, described in the appropriate place in
your observations.
(a) (i) FA 5, FA 6 and FA 7 are aqueous solutions each containing one anion and one cation.
Carry out the experiments described below and record your observations for each solution in
the table.
FA 5 FA 6 FA 7
To a 1 cm depth in a
test-tube, add a 1 cm
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depth of aqueous
sodium carbonate.
To a 1 cm depth in a
test-tube, add a 1 cm
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depth of aqueous
copper(II) sulfate.
To a 1 cm depth in a
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test-tube, add a 1 cm
depth of aqueous
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barium chloride or
aqueous barium nitrate.
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(iv) Write the ionic equation, including state symbols, for the reaction between FA 5 and
aqueous copper(II) sulfate.
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will dissolve.
• Filter the mixture into a clean boiling tube.
• Place the filter funnel in a conical flask and wash the residue with a little distilled water.
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• Keep both filtrate and residue for tests (i) and (ii) below.
t)
Carry out the following tests and record your observations in the table below.
test observations
To a 1 cm depth of the filtrate in a
test-tube, add aqueous sodium
hydroxide, then
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test observations
Place the funnel containing the
residue into a clean boiling tube. Pour
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(iii) Suggest what type of reaction is happening when hydrogen peroxide is added in test
(b)(i).
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.............................................................................................................................................[8][Total: 15]
t)
FA 5 FA 6 FA 7
+ no effervescence / effervescence
Na2CO reactio bubbling / fizzing / bubbling /
3
n or gas turns fizzing or gas
Fa
limewater turns
milky / cloudy limewater
white / white ppt milky / cloudy
white / white
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ppt
Percentage Purity
a)Titration Method You are required to find the percentage purity of a sample of sodium carbonate,
Na2CO3.
FA 1 contains 4.50 g dm–3 of the impure sodium carbonate.
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labelled FA 3.
Record your burette readings and the volume of FA 2 added to the flask in the space below.
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Make up the contents of the flask to the 250 cm3 mark with distilled water. Place the stopper in the flask and
mix the contents thoroughly by slowly inverting the flask a number of times.
Titration
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Fill a second burette with FA 3, the diluted solution of hydrochloric acid. Pipette 25.0 cm3 of FA 1 into a
conical flask. Add a few drops of methyl orange indicator and titrate with FA 3.
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Perform a rough (trial) titration and sufficient further titrations to obtain accurate results.
Record your titration results in the space below. Make certain that your recorded results show the precision of your
working.
(A
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[6]
t)
(b) From your titration results obtain a suitable volume of FA 3 to be used in your calculations.
Show clearly how you obtained this volume.
[1]
Calculations
Show your working and appropriate significant figures in all of your calculations.
(c) Calculate how many moles of HCl are contained in the FA 2 run into the graduated flask.
1.
Use this answer to calculate how many moles of sodium carbonate, Na2CO3, are present in 1.00 dm3 of FA
1.
Na2CO3 + 2HCl → 2NaCl + CO2 + H2O
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Calculate, to 3 significant figures, the percentage purity of the sodium carbonate, Na2CO3, dissolved in FA
1.
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(d) Look at the scale on the 25 cm3 measuring cylinder provided. Record the smallest scale division on the
measuring cylinder and estimate the error in reading the scale.
(A
before and titrate with FA 3. Repeat the titration once using the measuring cylinder. Record your results
below.
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Would you expect to be able to obtain consistent titres using a measuring cylinder? Explain your answer.
..........................................................................................................................................
t)
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(f) A student suspects that the presence of dissolved carbon dioxide affects the end-point of the titration.
Suggest a simple modification to the experimental technique to eliminate the dissolved carbon dioxide as the
titration is performed.
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Dear Students use 33.50 cm3 of FA2 in part (a) to prepare 250 cm3 of FA3 .
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measuring the temperature change when a weighed sample of the solid carbonate reacts with an excess of
hydrochloric acid and the following information is used.
Na2CO3(s) + 2HCl(aq) →2NaCl(aq) + CO2(g) + H2O(l) ΔH = –37.0 kJ mol–1
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• Support the plastic cup in the 250 cm3 beaker and add to it, from a measuring cylinder, 50 cm3 of FA 5.
• Measure and record the steady temperature of the FA 5 in the plastic cup.
• Add the FA 4 from the weighing bottle to the plastic cup, a little at a time to prevent acid spray. Stir and
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[4]
Calculations
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t)
(c) Is one repeat of the experiment sufficient or should it be repeated again? Explain your answer.
..........................................................................................................................................
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......................................................................................................................................[1]
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Dear students use 4.35 g of Solid and rise in temperature is 13.5 Co For Calculations Al-Chemist
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Enthalpy of Reaction
t)
You are required to determine the enthalpy change when citric acid reacts with an excess of sodium
hydrogencarbonate.
Citric acid, found in citrus fruit such as lemons and limes, is
2-hydroxypropane-1,2,3-tricarboxylic acid.
(a) Citric acid is a triprotic (tribasic) acid – one mole of the acid reacts with three moles of sodium
hydrogencarbonate.
Calculate the minimum mass of NaHCO that will react with all of the acid in 50.0 cm3 of FB 4.
iz
• Measure and record the steady temperature of the FB 4 in the plastic cup.
• Add the FB 5 from the weighing bottle, a little at a time, to the plastic cup.
• Stir and record the lowest temperature reached.
• Reweigh the empty weighing bottle.
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Empty and rinse the plastic cup. Repeat the experiment and calculate the mean value of ΔT.
Results
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(c) Calculate the enthalpy change of reaction using the following expression.
ΔHreaction = mean ΔT × 4.3 kJ mol–1
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Redox Titration
You are required to determine the concentration in g dm–3 of hydrated ammonium iron(II) sulphate,
(NH4)2SO4.FeSO4.6H2O, in the solution FB 1.
FB 1 contains hydrated ammonium iron(II) sulphate.
Fa
Record your burette readings and the volume of FB 1 added to the flask in the space below.
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Make up the contents of the flask to the 250 cm3 mark with distilled water. Place the stopper in the flask and
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mix the contents thoroughly by slowly inverting the flask a number of times.
Titration
Fill a second burette with FB 2.
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Pipette 25.0 cm3 of FB 3 into a conical flask. Use a measuring cylinder to add approximately 10 cm3 of 1.0
mol dm–3 sulphuric acid, H2SO4, and titrate with FB 2 until the first permanent pink colour remains in the
solution.
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Perform one rough (trial) titration and sufficient further titrations to obtain accurate results.
Record your titration results in the space below. Make certain that your recorded results show the precision
of your working.
(A
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[6]
(b) From your titration results obtain a suitable volume of FB 2 to be used in your calculations.
t)
[1]
Calculations
Show your working and appropriate significant figures in all of your calculations.
(c) Calculate how many moles of KMnO4 were run from the burette during the titration.
........................ mol of Fe2+ reacted with the KMnO4 run from the burette.
Calculate the concentration, in mol dm–3, of Fe2+ in FB 3.
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(f) A titre value is obtained by the difference between final and initial burette readings.
What is the maximum possible error in obtaining a titre reading?
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Dear Students , Use 36.50 cm3 of FB1 and 19.65 cm3 of FB3 Al-Chemist
Remember in your Prayers Faiz Ul Hassan
Iodometric Titration
You are required to find the concentration in mol dm–3 of sodium thiosulphate, Na2S2O3, in solution FB 1.
FB 1 contains sodium thiosulphate.
FB 2 is potassium manganate(VII) containing 28.44 g dm–3 KMnO4.
Fa
Dilution of FB 2
(a) By using a burette measure between 41.00 cm3 and 42.00 cm3 of FB 2 into the 250 cm3 graduated
(volumetric) flask labelled FB 5.
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Record your burette readings and the volume of FB 2 added to the flask in the space below.
lH
Make up the contents of the flask to the 250 cm3 mark with distilled water. Place the stopper in the flask and
mix the contents thoroughly by slowly inverting the flask a number of times.
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Titration
Fill a second burette with FB 1, the solution containing sodium thiosulphate.
Use a measuring cylinder to transfer 10 cm3 of FB 3 and 10 cm3 of FB 4 into a conical flask. Pipette 25.0
cm3 of FB 5 into the conical flask containing the mixture of FB 3 and FB 4.
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The potassium manganate(VII) oxidises potassium iodide to iodine, I2. Titrate the liberated iodine with FB 1
as follows. Run the solution from the burette into the conical flask until the initial red/brown colour of the
iodine becomes pale yellow.
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Then add 1 cm3 of the starch indicator and continue to add FB 1 drop by drop until the blue/black colour of
the starch/iodine complex disappears, leaving a colourless solution. This is the end-point of the titration.
(A
Perform a rough (trial) titration and sufficient further titrations to obtain accurate results.
Record your titration results in the space below. Make certain that your recorded results
show the precision of your working.
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[6]
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(b) From your titration results obtain a volume of FB 1 to be used in your calculations.
Show clearly how you obtained this volume.
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Calculations
Show your working and appropriate significant figures in all of your calculations.
(c) Calculate how many moles of KMnO4 are contained in the FB 2 run into the graduated flask.
[A r: K, 39.1; O, 16.0; Mn, 54.9]
Use this answer to calculate how many moles of iodine molecules, I2, are formed when the manganate(VII)
ions react with an excess of iodide ions in the titration flask.
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formed.
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………………….. mol of thiosulphate ions react with the iodine molecules formed in the reaction.
Calculate, to 3 significant figures, the concentration in mol dm–3 of the sodium thiosulphate, Na2S2O3, in FB
1.
sa
You are to determine the relative molecular mass, Mr, of the acid and deduce its molecular formula.
You are provided with the following.
FA 1, the aqueous acid, containing 38.68 g dm–3 RCO2H
FA 2, aqueous sodium hydroxide containing 3.40 g dm–3 NaOH
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Phenolphthalein indicator.
(a) Dilution of FA 1
By using a burette measure between 38.00 cm3 and 39.00 cm3 of FA 1 into the 250 cm3 graduated
he
Make up the contents of the flask to the 250 cm3 mark with distilled water. Place the stopper in the flask and
t)
mix the contents thoroughly by slowly inverting the flask a number of times.
Titration
Fill a second burette with FA 3, the diluted solution containing RCO2H.
50 Faiz Ul Hassan Khan (Al-Chemist) )0321-9070007
Resource Pack By Faiz Paper 3 Practice Notes Al-Chemist
Pipette 25.0 cm3 of FA 2 into the conical flask and add 2–3 drops of phenolphthalein indicator.
Titrate the sodium hydroxide in the flask with FA 3 until the solution just turns colourless.
Perform a rough (trial) titration and sufficient further titrations to obtain accurate results.
Record your titration results in the space below. Make certain that your recorded results
show the precision of your working.
Fa
iz
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[6]
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as
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(b) From your titration results obtain a volume of FA 3 to be used in your calculations. Show clearly how
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Calculations
Show your working and appropriate significant figures in all of your calculations.
(c) Calculate how many moles of NaOH have been pipetted into the conical flask.[Ar: H, 1.0; O, 16.0; Na,
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23.0]
Use your titre volume in (b) and the answer above to calculate how many moles of RCO2H are contained in
250 cm3 of the diluted acid FA 3.
Use this answer to calculate the concentration, in mol dm–3, of the undiluted acid in FA 1. The concentration
of
is
t)
sulphate, MgSO4.xH2O.
The water contained in the crystals can be removed by heating the crystals.
Method
(a) Follow the instructions below to determine the mass of water driven off when heating magnesium
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sulphate crystals.
• Weigh the empty hard glass boiling-tube.
• Tip the contents of the tube labelled FA 4 into the boiling-tube.
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Results
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(A
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[7]
Calculations
(b) Calculate the percentage by mass of water of crystallisation in the crystals.
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(c) Use the relative molecular mass information provided to complete the table below.
[Mr: MgSO4, 120.4; H2O, 18.0]
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t)
Use your answer in (b) and the information in the table to find the experimental value of x in the formula
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MgSO4.xH2O.
(d) A student is instructed to repeat the whole experiment to ensure reliability of results. Explain how
repeating the experiment would lead to greater reliability in the experimental results.
(A
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(e) On a balance weighing to 1 decimal place assume the maximum error is ±0.1 g. What mass would
have to be weighed out on this balance to result in an error of 0.04%?
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b) By titration method
FA 1 is an aqueous solution containing 38.10 g dm–3of borax crystals. Borax has the formula,
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Na2B4O7.xH2O.
FA 2 is 1.00 mol dm–3 hydrochloric acid, HCl.
t)
You are also provided with an indicator suitable for the titration of a strong acid and a weak base.
The indicator provided is ..............................................................
(a) Method
Dilution
• Fill the burette with FA 2.
• Run between 44.50 cm3and 45.50 cm3of FA 2 from the burette into the 250 cm3
graduated (volumetric) flask, labelled FA 3.
Fa
Titration
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• Titrate the borax in the flask with FA 3 until the appropriate colour change isobserved for the end-point.
You should perform a rough titration.
In the space below record your burette readings for this rough titration.
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(A
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• Carry out as many accurate titrations as you think necessary to obtain consistent results.
• Make certain any recorded results show the precision of your practical work.
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• Record in a suitable form below all of your burette readings and the volume of FA 3 added in each
accurate titration.
t)
[7]
(b) From your accurate titration results obtain a suitable value to be used in your calculations.
Show clearly how you have obtained this value.
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(c) Calculations
Show your working and appropriate significant figures in the final answer to each step of your calculations.
(i) Calculate the concentration of hydrochloric acid, in mol dm–3, in the diluted solution, FA 3.
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(A
(ii) Calculate how many moles of HCl were present in the volume of FA 3 calculated in (b).
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(iii) Calculate how many moles of Na2B4O7 reacted with the HCl in (ii).
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t)
The HCl run from the burette reacted with ………………….. mol of Na2B4O7.
(iv) Calculate the concentration, in g dm–3, of Na2B4O7 in FA 1.[Ar: B, 10.8; O, 16.0; Na, 23.0]
(v) Use your answer to (iv) and the information at the start of question 1 to calculate
the percentage by mass of water in the borax crystals, Na2B4O7.xH2O.[Ar: H, 1.0; B, 10.8; O, 16.0; Na,
23.0]
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(d) The maximum error for a 25 cm pipette commonly used in schools is ±0.06 cm3.
3
Dear Students, consider 45 cm3 of FA2 during dilution and 23.50 cm3 of FA3 for calculations. Al-
Chemist
(A
Back Titration
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In step two, you will carry out a titration to find the amount of acid you used in step one.
In step three, you will carry out a second titration to find how much (excess) acid remained
following the reaction in step one.
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Finally, you will use the values found in the three steps to calculate the percentage purity of the calcium
carbonate.
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Assume the impurity in the calcium carbonate will not react with acid or alkali.
FA 1 is 0.100 mol dm–3 sodium hydroxide, NaOH.
t)
(a) Method
Step 1
● Fill the burette labelled FA 2 with FA 2.
● Run 50.00 cm3 of FA 2 into a 250 cm3 beaker.
● Weigh the tube containing the impure calcium carbonate, FA 4.
● Tip the contents of the tube, in small portions, into the acid to avoid acid spray. Stir
Fa
Step 2
● Fill the burette labelled FA 1 with FA 1.
● Pipette 25.0 cm3 of FA 3 into a conical flask.
● Add methyl orange indicator.
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● Perform a rough titration and record your burette readings in the space below.
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(A
● Make certain any recorded results show the precision of your practical work.
● Record in a suitable form below all of your burette readings and the volume of FA 1
added in each accurate titration.
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m
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t)
Step 3
● Stir the mixture from Step 1 again to ensure that all the solid has dissolved.
● Transfer the solution to the 250 cm3 graduated (volumetric) flask labelled FA 5.
● Rinse the beaker twice with a little distilled water and add the washings to the graduated flask.
● Make the solution up to 250 cm3 with distilled water. Ensure that the contents of the
flask are thoroughly mixed.
● Transfer 25.0 cm3 of this solution, FA 5, into a second conical flask using a second pipette.
● Perform a rough titration and record your burette readings in the space below.
Fa
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● Make certain any recorded results show the precision of your practical work.
● Record in a suitable form below all of your burette readings and the volume of FA 1 added in each
accurate titration.
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(A
[12]
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Calculations
Show your working and appropriate significant figures in the final answer to each step of your calculations.
The equation for the reaction between sodium hydroxide and hydrochloric acid is shown below.
NaOH(aq) + HCl (aq) → NaCl (aq) + H2O(l)
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(b) (i) From your accurate titration results in Step 2, obtain a suitable value to be used in
your calculations. Show clearly how you have obtained this value.
m
(ii) Use your answer from (i) to calculate the number of moles of sodium hydroxide,
FA 1, required to react with 25.0 cm3 of FA 3 in Step 2.
t)
(iv) Use your answer from (iii) to determine the number of moles of hydrochloric acid in
250 cm3 of FA 5.
(A
(d) (i) Write an equation for the reaction between calcium carbonate and hydrochloric acid.
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(ii) Calculate the number of moles of hydrochloric acid that reacted with calcium
carbonate in FA 4 using the following expression.
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(iii) Use your answers from (i) and (ii) to calculate the mass of CaCO3 in FA 4.[Ar: C, 12.0; O, 16.0; Ca,
40.1]
(If you were unable to answer (d)(ii), you may assume that the number of moles of
hydrochloric acid that reacted with calcium carbonate was 0.0351 mol.)
(ii) Calculate the maximum percentage error for one of your accurate titres in Step 3.
Show your working.
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Accuracy A measure of the closeness of agreement between an individual result and the
accepted value. An accurate result is in close agreement with the accepted value.
Error The difference between an individual measurement and the true value (or
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within which the true value is said to lie. It is written, for example, as 44.0 ± 0.4.
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Reliability The opposite of uncertainty; high uncertainty = not very reliable measurement
Accuracy of measurements
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Uncertainty is often taken to be half a division on either side of the smallest unit on the scale.
However, the accuracy of measurements also depends on the quality of the apparatus used
Dear Students , This booklet is not complete yet, so kindly check my class notes ( practical notes) and feel
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67.36 67.356
2-places 3-places
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3 3 3
26.50 cm 3.00 cm 2.45 cm
Maximum errors
3
Burette • graduated in divisions every 0.1 cm
3
• maximum error is half a division i.e. ± 0.05 cm
3
• burettes are read twice, so the overall maximum error is 2 x 0.05 = ± 0.1 cm
Fa
3 3
Pipette • a 25 cm pipette has a maximum error of 0.06 cm
• like all volumetric equipment it must be used properly
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Dear Students , this practical booklet is not complete yet so use my class lectures (notes ) too.
Feel free to ask any question (Past papers, from My AS chemistry booklet 497 pages only or course book etc)
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