SMC Chemistry Sba Module Draft
SMC Chemistry Sba Module Draft
Results
Treatment of results
Procedure 1. How many components are present in black ink?
1. Draw a horizontal pencil line about 1.5 cm from the bottom
edge of the chromatography paper. This is the origin. 2. Find the Rf (retention factor) of each component as follows:
2. Apply the black ink to the pencil line using the fine Rf value = distance moved by the component from origin
capillary tube as follows. Touch the capillary tube to the distance moved by the solvent from origin
surface of the black ink so that only a little is drawn up the
tube and apply the dye to paper using a quick 3. Which of the dyes in black ink is more soluble in water?
Explain your answer.
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2. Clamp the boiling tube and its contents vertically in water Solubility of potassium nitrate (g/100 g water) =
bath and warm carefully, while stirring, until all the solid 𝑚𝑎𝑠𝑠 𝑜𝑓 𝑝𝑜𝑡𝑎𝑠𝑠𝑖𝑢𝑚 𝑛𝑖𝑡𝑟𝑎𝑡𝑒
× 100
dissolves. 𝑚𝑎𝑠𝑠 𝑜𝑓 𝑤𝑎𝑡𝑒𝑟
3. Place the thermometer into the boiling tube and after a few Assume 1 cm3 = 1 g
minutes remove the boiling tube from the water bath.
Allow the boiling tube and its contents to cool, stirring
gently with the thermometer. Record the temperature at Treatment of results
which crystals first appear.
1. Plot a graph of solubility of potassium nitrate in g per 100
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4. Add to the contents of the boiling tube a further 2.0 cm of cm3 of water against temperature in oC.
distilled water and repeat the above procedure, noting the
temperature at which the crystals first appear. 2. What deductions can you draw from the graph?
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Electronic Scale
3. Calculate the number of moles of chalk used to write your
Procedure: name. Show your work.
4. Again, measure and record the mass of your chalk. Source of errors?
Results:
Procedure:
1. Measure 25 cm3 of solution A using a measuring cylinder.
2. Pour this solution B into a plastic cup.
3. Fill a burette with solution B.
4. Add 5cm3 of solution B to solution A. Stir and record highest
temperature observed.
5. Repeat step 4 above until 50cm3 of solution B has been added.
6. Repeat steps 1-5 and calculate the average temperatures
Results:
Total Volume of B Temperatures (0C)
added (cm3)
1st run 2nd run Average
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Titration
Burette readings/cm3
Apparatus and Materials: Rough 1 2 3
Sodium hydroxide solution Final reading
0.1 mol dm-3 hydrochloric acid solution
Initial reading
conical flasks
50 cm3 burette Volume of HCl used /
25 cm3 pipette cm3
Methyl orange indicator
Treatment of Results
1. Calculate the average volume of hydrochloric acid.
Procedure
1. Wash the burette thoroughly with liquid detergent. 2. Find the number of moles of hydrochloric acid in the
Wash it with tap water and then with distilled water and average volume used.
finally rinsed with hydrochloric acid solution. Fill the
burette to convenient mark with hydrochloric acid. 3. Write a balanced equation for the reaction.
Record this reading.
4. Use the equation to find the number of moles in 25 cm3 of
2. Pipette 25.0 cm3 of sodium hydroxide into a conical sodium hydroxide solution.
flask, add 1 – 2 drops of methyl orange indicator, and
add hydrochloric acid from the burette until the end- 5. Calculate the concentration of sodium hydroxide solution
point is reached. Record this reading. in
(i) mol dm-3
3. Repeat the titration as many times as convenient, until (ii) g dm-3
consecutive burette readings differ by no more than ±
0.10 cm3. 6. Identify errors in the experiment.
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Procedure:
1. Measure 5 cm3 of hydrochloric acid using a measuring cylinder.
2. Pour this volume of acid into a clean test tube.
3. Place a small sample of iron into the test tube containing the
hydrochloric acid.
4. Immediately place a lighted splint into the mouth of the test tube
and listen carefully.
5. Record all observations in a suitable table.
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Procedure:
1. Using a pipette, transfer 25cm3 of BA1 to a conical flask
and titrate with BA2from the burette. The end-point is
reached when the solution just turns pink.
Results
Readings/cm3 Trial 1 2
Initial
Final
Volume Used
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Apparatus and Materials 7. Carry out five (5) further experiments, increasing the
temperature by about 5 oC each time.
0.1 mol dm-3 sodium thiosulphate (VI)
2.0 mol dm-3 nitric acid
Results
Stop clock
Measuring cylinders 1. Tabulate your results as follows:
250 cm3 beaker
Temperature/oC Time/s Rate (1/s)
Sheet of paper with a cross drawn on it
Thermometer 30
Bunsen burner
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Procedure 40
3
1. Using measuring cylinders, transfer 50 cm of water to a 45
250 cm3 beaker, then add 25 cm3 of the sodium
thiosulphate solution. 50
Procedure:
1. Sanitize the nichrome wire by dipping it into a sample of
concentrated HCl and hold it in a flame for a few seconds.
2. Take a small sample of M1 using the end of the nichrome
wire, and place the sample into the flame.
3. Observe and record the colour of the flame.
4. Repeat steps 1-3 for the other metals
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Procedure:
1. Set up the electrolytic cell circuit as shown in the diagram
below:
2. Observe and record all activity and changes occurring at each
of the electrodes.
3. Observe and record any changes occurring in the electrolyte.
Results:
Site Observations
Anode
Cathode
Electrolyte
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Procedure:
1. Measure and record the initial mass of each electrode.
2. Set up the electrolytic cell circuit as shown in the diagram
below:
3. Allow the current to flow through the electrolyte for 10
minutes and record all observations.
4. Measure and record the final mass of each electrode.
5. Calculate the change in mass of each electrode.
Results:
Electrode Initial Final Change in
Mass(g) Mass(g) Mass (g)
Anode
Cathode
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Treatment of results
1. Record your results as follows:
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Procedure:
1. Measure out 30 g into a 250 mL beaker.
2. Heat the coconut oil until it melts completely; you may need to
swirl to get everything to melt. Once it is completely melted turn off
the Bunsen burner.
3. Measure out 33 g of water into the 150 mL beaker.
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General Criteria:
5. Expected Results: This is a prediction of the
1. Hypothesis: This must be based on observations and observations that should be made, based on the
clearly stated in a form that is testable. hypothesis that is being tested. A statement of how these
results will support the hypothesis written.
2. Aim: Must be linked to the hypothesis.
3. Apparatus and Materials: These must be listed and 6. Limitations, sources of errors: A restrictive condition or
appropriate for the method or procedure suggested. variable which cannot be controlled and which can affect
the validity of the results.
4. Method: This involves:
Steps to be followed in appropriate sequence/ how the
apparatus and materials will be used. 7. Assumptions: The supposition that something is true. A
statement taken for granted without evidence.
Precautions
Treatment of variables
Type of data to be collected and how they will be
treated
Variables
Manipulated/Independent Variable – the variable
that is manipulated or change in a controlled way.
Responding/Dependent Variable – the variable that
is being measured. It is a change that results from
manipulation of the independent variable.
Controlled/Constant Variable – The variables that
are kept constant throughout the experiment so that
they do not affect the outcome of the experiment.
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EXAMPLE 1
Plan and design an investigation to find out if ‘black ink’ from Variables
different brands of permanent markers contains the same dyes
Controlled Variable - size of chromatography paper
(permanent means that the ink is insoluble in water).
No. of drops of ink used
Hypothesis The black ink from different brands of permanent
markers contains the same dyes. Volume of alcohol
Aim To separate the dyes from four different brands of Manipulated Variable - Brands of permanent markers
black ink using paper chromatography. Responding Variable - Colours and position of dye.
Apparatus and Materials
o Four identical boiling tubes with stoppers and hooks Expected Results
o Rubbing alcohol
o Measuring cylinder If the colour of the spots and their Rf values are the same for each
o Chromatography paper brand then the hypothesis is supported (valid).
o Four (4) different brands of permanent markers
Procedure
Cut four (4) pieces of chromatography paper 2 cm x 8 cm. Limitations/ Source of Errors
Draw a line 1 ½ cm from one end of each piece of paper. If the newspaper is used instead of chromatography paper, the
Using one piece of paper for each brand of ink, put one spot spots may not separate completely. The spot of ink may not have
of the same size in the middle of the line drawn. been exactly the same size.
Measure the volume of the alcohol needed and pour this
volume into each test tube. Label the tubes W, X, Y and Z to
match the brands.
Assumptions
When the alcohol reaches the top of the strip, remove each
chromatogram and allow it to dry. Rubbing alcohol is an effective solvent for the different brands of
Note the colours and positions of the spots. black ink.
Calculate the retention factor (Rf value) for each spot.
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EXAMPLE 2
Problem Statement: 3. Prepare the water to the following temperatures, 0
degrees Celsius (use ice), room temp 30 degrees Celsius,
You are given a salt and asked if the salt will dissolve in 4. 60 degrees Celsius (warm slightly) and 90 degrees
water more at high temperatures. Celsius (boil).
5. Place the salt in each container of water and stir for 20
Hypothesis: The salt will dissolve more at room temperature. seconds.
6. Allow the residue to dry and reweigh.
Aim: To determine the solubility of a salt at different
temperatures Variables:
Apparatus and Materials:
Control variable: volume of water, amount of salt and time
Electronic balance
Sodium chloride Manipulated Variable: temperature
Measuring cylinder
Responding Variable: the amount of salt that remains
Thermometer
undissolved.
Bunsen burner
Tripod Expected Results: If the mass of the residue is highest at
Gauze room temperature then the hypothesis is valid.
Stirring rod
Beakers Limitation: It was difficult to remove all the sodium chloride
Filter paper from the beaker.
Funnel
Source of Error: Parallox error
Method:
Assumption: High temperatures increase the solubility of
1. Weigh out four equal amounts 15 g of the salt. sodium chloride.
2. Measure out four equal volumes of 20 cm3 of water.
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ethanoic acid than commercial brands of vinegar. Design experimental data obtained from the heating of water by
an experiment to test the validity of Aunt Mavis’s claim. the fuels.
Using the information above, plan and design an
4. Sally, a cleaner was preparing to clean Miss George’s experiment to determine whether kerosene and
home. She usually cleans the kettle with vinegar and the methylated spirit produce the same amount of energy on
tiles with muriatic acid (hydrochloric acid). However, the combustion.
labels from the bottle containing the cleaning agents were
removed. Sally attempted to distinguish these two 2. Charles, reacting to what he learnt on the top
cleaning agents by smelling, however she was still “Energetics”, hypothesized that the energy value of an
unsure. alcohol depends on the number of carbon atoms it
Plan and design an experiment that can be used to contains. Design an experiment to test the validity of
undertake in the laboratory to determine which bottle Charles’s hypothesis.
contains the vinegar and which contains muriatic acid.
Alcohols
Electrolysis
You are provided with three brands of beer, namely Carib,
Compounds can be classified as electrolytes and non- Heineken and Piton. Plan and design an investigation to find out
electrolytes. Electrolytes can be further classified as weak or which beer has the highest percentage alcohol content.
strong electrolytes.
You are provided with sodium chloride, hydrochloric acid,
sucrose and ethanoic acid. Plan and design an experiment to
determine the respective category of the compounds.
Energetics
IDENTIFICATION OF CATIONS
Test with NH4OH(aq)
Test with NaOH(aq)
Cation Observation with NH4OH (aq) Ionic Equations
Cation Observation with NaOH (aq) Ionic Equations
Ca2+ No precipitate.
Ca2+(aq) + 2OH-
White precipitate. Precipitate White precipitate. Precipitate
Ca2+ (aq) → Zn2+
insoluble in excess NaOH. soluble in excess NH4OH
Ca(OH)2(s)
Al3+(aq) + 2OH-
Al3+
White precipitate. Precipitate (aq) →
Pb2+ Al3+
soluble in excess NaOH White precipitate. Precipitate Al(OH)3(s)
Zn2+ Pb2+
insoluble in excess NH4OH Pb2+(aq) + 2OH-
Cu2+(aq) + 2OH-
Blue precipitate. Precipitate (aq) →
Cu2+ (aq) →
insoluble in excess NaOH Pb(OH)2(s)
Cu(OH)2(s)
Blue precipitate. Precipitate
Dirty green precipitate. Fe2+(aq) + 2OH- 2+
Cu soluble in excess NH4OH
Fe2+ Precipitate insoluble in excess (aq) →
firming a deep blue solution.
NaOH Fe(OH)2(s)
Dirty green precipitate. Fe2+(aq) + 2OH-
Fe3+(aq) + 3OH-
Orange precipitate. Precipitate Fe2+ Precipitate insoluble in excess (aq) →
Fe3+ (aq) →
insoluble in excess NaOH NH4OH Fe(OH)2(s)
Fe(OH)3(s)
Fe3+(aq) + 3OH-
No precipitate – NH3(g) evolved Orange precipitate. Precipitate
NH4+ Fe3+ (aq) →
on warming insoluble in excess NH4OH
Fe(OH)3(s)
IDENTIFICATION OF ANIONS
Effect of Heat
Effect of silver nitrate, AgNO3(aq) followed by NH4OH(aq)
Heat a sample of solid in a dry test tube.
Anions Effect of Effect of Ionic Equations
Anions Observation Inference AgNO3(aq) NH4OH(aq)
CO32- Gas evolve forms white CO2(g) Cl- White Precipitate Ag+(aq) + Cl-(aq)
precipitate with lime water, precipitate – soluble → AgCl(s)
Ca(OH)2 turns purple in
sunlight
Br- Cream Precipitate Ag+(aq) + Br-(aq)
NO3- (of K Gas evolved relights a glowing O2(g) precipitate slightly soluble → AgBr(s)
or Na) splint. I- Pale yellow Precipitate Ag+(aq) + I-(aq)
precipitate insoluble → AgI(s)
O2(g) and
NO2(g) Effect of barium nitrate, Ba(NO3)2(aq)or barium chloride,
-
NO3 (of Gas evolved relights a glowing BaCl2(aq) solution followed by dilute acid.
Ca and splint, also a red brown
below in colour gas evolved turns blue
the litmus red then bleaches it. Anions Effect of Effect of Ionic Equations
reactivity Ba(NO3)2(aq) or HCl(aq) or
BaCl2(aq) HNO3(aq)
series)
CO32- White precipitate Precipitate Ba2+(aq) + CO32- (aq)
SO32- Gas evolved has a chocking SO2(g) soluble → BaCO3(s)
smell, turns acidified SO32- White precipitate Precipitate Ba2+ (aq) + SO32- (aq)
KMnO4(aq) from purple to soluble → BaSO3 (s)
colourless, turns acidified SO42- White precipitate Precipitate Ba2+ (aq) + SO42- (aq)
K2Cr2O7(aq) from orange to insoluble → BaSO4 (s)
green.
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IDENTIFICATION OF GASES