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Results: where tables are used they must have a proper title that is not ambiguous e.g ‘THE
TITRE VALUES OBTAINED DURING THE NEUTRALIZATION OF 0.1M NaOH’ and
NOT ‘RESULTS OBTAINED DURING EXPERIMENT’. You can use more than one table
if needed. If do number your tables. Eg ‘TABLE 1: OBSERVATIONS OF METTALLIC
ION FLAME COLOR’
Sources of Error/limitations/assumptions:
Table of contents
Problem Statement/Observation:
Title:
Date:
Hypothesis:
Aim:
Variables:
• Controlled
• Manipulated
• Responding
Method:
Expected results: (tabular form for display of results and a sentence or two stating what you
are expecting based on your hypothesis)
Treatment of results:
Discussion:
Bunsen burner
Safety glasses
Beaker with water
Wooden splints
Solutions (1.0 mol/L) of the following metal salts
barium chloride
calcium chloride (cobalt chloride substituted)
copper(II)chloride
sodium chloride
potassium chloride
magnesium chloride
zinc chloride
iron (II) chloride
sodium chloride /potassium chloride mixture
unknown A
unknown B
Procedure:
1. Work in pairs to carry out the test on each solution at the workstations set up.
2. At your first workstation, light the Bunsen burner and open the air vent to obtain a non-luminous
flame with two blue cones.
3. Remove one of the wooden splints that have been soaking in the metal salt solution labeled on the
beaker
4. Carefully place the end of the wooden splint that was soaked in the metal salt solution at the top of
the inner blue cone. Record the color and intensity (bright/faint) of the flame in the data table. The
color given off by the salt is the initial color observed, not the yellow-orange color produced by the
burning wood. (To avoid burning the wood, wave the splint through the flame rather than holding
it right in the flame).
5. If more observations are needed, dip the clean end of the wooden splint in the solutions for a few
minutes and repeat. Otherwise, discard the wooden splints in beaker of water at the end of the
experiment.
6. Repeat with the other salts at the different workstations. Be sure to record the colors as precisely as
possible
Results: Record your results in a suitable table
Discussion:
Analyze the data obtained using the following questions as guidelines. Questions do not have to
be answered in the order given but you should organize your discussion so that it flows. From
one point to the next.
1. Explain how the colors observed in the flame tests are produced.
2. Why do different chemicals emit different colors of light?
3. List the colors observed in this lab from the highest energy to the lowest energy.
4. List the colors observed in this lab from the highest frequency to the lowest
frequency.
5. List the colors observed in this lab from the shortest wavelength to the longest
wavelength.
6. What is the relationship between energy, frequency, and wavelength?
7. Based on the results of your experiment, what metal is found unknown A and
unknown B? Explain.
8. Can a flame test be used to determine the identity of unknowns in a mixture? Why or
why not? (refer to results from the experiment)
9. Account for cases where a distinct flame color and intensity was not observed.
10. Give relevant sources of errors (at least 2) and limitations.
Apparatus/ material: Solid samples of A, B, C and D, 12 test tubes, test tube rack and
holder, glass rod, 25cm3 measuring cylinder, spatula, Bunsen Burner, electrical circuit,
propanone, distilled water.
Method:
1. Add a small spatula of sample A to a test tube and heat gently at first and then strongly
until no further change is observed.
2. Add a small spatula of sample A to 20cm3 of distilled water in a test tube. Test the
resulting mixture for electrical conductivity. Record your observations on solubility and
electrical conductivity.
3. Repeat step 3 using propanone instead of water.
4. Repeat steps 1 – 3 using samples of B, C and D.
Conclusion:
LAB 3 (P&D # 1)
Problem Question:
John and Sarah are interested in the oxidizing abilities of Cu2+, Pb2+ and Ag+. Plan and design
an experiment to compare the relative oxidizing abilities of these metal ions.
Title:
Aim:
Apparatus/Materials:
Variables: Independent variable (the one you are controlling), Dependent variable (the one
you will be recording results for), Controlled variables (all other variables that must be kept
constant)
Method:
Present tense
Expected results: shows how results will be recorded (tables, graphs etc), if tables are being
used then draw empty tables with headings and title.
Treatment of results: If graphs are being used state which variable should be plotted on
which axis.
Discussion: Explain the results that should be expected (if known) and write relevant
equations.
Apparatus/ Material:
A1 – 0.1 moldm-3 HCl (100 cm3), B1- Solution containing 60gdm-3 Na2CO3/NaCl mixture (40
cm3), methyl orange indicator, 250cm3 volumetric flask, 25cm3 pipette, two 50 cm3 burette,
three 250 cm3 conical flask, funnel, White tile, wash bottle with distilled water.
Method:
1. Using a burette, place 30.00 cm3 of B1 in a 250cm3 graduated flask. Make up the contents
of the flask to the mark using distilled water to produce B2.
2. Place A1 in a second burette.
3. Pipette 25cm3 of B2 into a conical flask. Add 2 drops of methyl orange indicator and titrate
with A1 until the first permanent color change is observed.
Treatment of results/calculations
Discussion
Points to include:
Definition of titration.
Explanation of the reaction occurring.
Concept of end point/equivalence point (in relation to the titre value obtained) and
choice of indicator.
Why titration is a suitable method.
Sources of error: At least 2 appropriate.
Conclusion:
Lab 5
Materials/ apparatus:
0.020 moldm-3 potassium manganate (VII) solution (75 cm3), H2O2 stock solution (10cm3),
1M sulphuric acid solution (40cm3) distilled water, 250cm3 volumetric flask (1), beakers to
collect solutions (3), conical flasks (3), 50cm3 burette (1), 25 cm3 pipette (1), pipette filler,
white tile, retort stand, 10 ml measuring cylinder (2)
Procedure
1. Prepare 250 cm3 of a solution of hydrogen peroxide by adding 7.5 cm3 of the stock solution
supplied to the volumetric flask and diluting to the required volume.
2. Pipette 25.0 cm3 of this solution into a conical flask.
4. Titrate the mixture against the potassium manganate (VII) until a permanent pale pink
colour appears in the conical flask.
5. Record the titre volume and repeat until concordant values are obtained.
6. Write your results in the table below and answer the questions that follow.
Results
Burette Trial 1 2
Reading/cm3
Final
Initial
Volume
used/cm3
Treatment of results/Calculations
2. Using the two half equations from question 1, write the full balanced ionic equation.
3. If the stock solution of hydrogen peroxide had a molar concentration of 1.67 mol dm-
3
, determine the molar concentration of the hydrogen peroxide solution prepared by
you.
4. Determine the molar concentration of the hydrogen peroxide solution prepared by you
using your titration results.
5. Hydrogen peroxide is sold using terms such as “20-volume”. This means that any
volume of H2O2 will decompose the produce 20 times that volume of oxygen gas (eg.
1cm3 of hydrogen peroxide would produce 20 cm3 of oxygen upon decomposition).
Using the molar concentration of the stock solution of 1.67 mol dm-3, determine what
designation you would assign this hydrogen peroxide.
1. Relevant definitions
2. Make reference to relevant equations to identify
Changes in oxidation states,
what is oxidized/ reduced
oxidizing and reducing agents
3. Account for any differences in values for 3 and 4 under treatment of results.
4. Sources of errors/
Conclusion:
LAB 6 (To be done in groups of 4)
Skill assessed: MM
N.B. For your M/M skill, you will be assessed on your use of the top loading balance, as
well as general lab measurement skills (measuring cylinder, thermometer readings, use
of reagents etc.)
NaOH rapidly absorbs moisture from the air to form a corrosive liquid so conduct this
part of the experiment quickly but carefully! The persons weighing the NaOH must
wear gloves!
Aim: To determine the standard enthalpy changes of solution, neutralization and reaction for
sodium hydroxide and use them to verify Hess’ law.
Apparatus: Top loading balance, spatula (will be in container with NaOH), weighing paper
(2), solid sodium hydroxide, 2M sodium hydroxide solution (100 ml), 2M hydrochloric acid
(100ml), 0.25M hydrochloric acid (200ml), thermometer (2), styrofoam cup (3), 250 - 300 ml
beaker (6), 100 ml measuring cylinder (1), distilled water (200ml), 50ml burette (1), 25ml
pipette (1), pipette filler (1), retort stand and clamp (1), funnel (1)
Method:
Results:
Record your results in suitable tables. Ensure that your tables are numbered, enclosed,
easy to read, have suitable titles that are underlined, have suitable headings and units.
Draw a graph of temperature (y-axis) vs volume of 2M HCl added (x – axis) for the
standard enthalpy of neutralization. From your graph determine the equivalence point
of the titration and clearly label this point on your graph.
Calculations:
1. Calculate the standard enthalpy changes of neutralization, solution and reaction using
your knowledge of energetics and the results obtained from the experiments (Assume
the specific heat capacity of the polystyrene cup is negligible and that the specific heat
capacity of the solution is 4.18JK-1g-1.) For the standard enthalpy change of reaction,
determine which reagent is limiting and use its number of moles to calculate the
standard enthalpy change of reaction.
2. Write the net ionic equations for all reactions
3. Use your ionic equations for neutralization and solution to construct a Hess’ law
diagram to determine the value for the enthalpy change of reaction for sodium
hydroxide with hydrochloric acid
4. Use your Hess’ law diagram along with the calculated values for standard enthalpy
change of neutralization and solution to calculate a second value for the standard
enthalpy change of reaction for sodium hydroxide with hydrochloric acid.
Discussion:
Comparisons between the value for the enthalpy of reaction calculated from the
experiment with that obtained using Hess’ law and account for any differences
Comparisons between your experimental values for each enthalpy with theoretical
ones and account for any differences.
Conclusion:
LAB 7 (P&D#2)
Problem:
The substance hydrogen peroxide decomposes naturally to water and oxygen gas. You are
given THREE substances X, Y and Z and are told that they catalyse the decomposition
process of hydrogen peroxide. Your task is to determine which of the three substances is the
most efficient catalyst.
Title:
Aim:
Apparatus/Materials:
Method:
Present tense
Variables: Independent variable (the one you are controlling), Dependent variable (the one
you will be recording results for), Controlled variables (all other variables that must be kept
constant)
Expected Results
Based on the method, what data can you collect? This is basically the responding variable.
Shows how results will be recorded (tables, graphs etc), if tables are being used then draw
empty tables with headings and title.
If graphs are being used state which variable should be plotted on which axis.
Expected Results and Treatment of Results are two different criteria. In the latter criterion,
students must describe how they will use the results obtained to solve the problem.
This would include details of the calculations that must be done (if applicable) and inferences
that can be made.
Discussion: Explain the results that should be expected (if known) and write relevant
equations.
1. Measure 50ml of sodium thiosulphate into the 50ml measuring cylinder and then add
it to the beaker.
2. Place the conical flask/beaker on a paper given.
3. Record the initial temperature of the sodium thiosulphate solution
4. Measure 25 ml of 0.5M HCl into a 25ml measuring cylinder
5. Add the HCl to the conical beaker and immediately start timing
6. Swirl the contents of the flask/beaker once and let it stand on the white tile
7. Stop timing when the writing on the paper is no longer visible through the solution
8. Record the time taken in seconds
9. Wash the solution down the sink with plenty of water
10. Repeat the experiment at three different concentrations of sodium thiosulphate (refer
to the results table)
11. Use 1/time taken as a measure of the relative rate
N.B. Add the required volume of thiosulphate to the 50ml measuring cylinder and then
make it up to the 50 ml mark with distilled water, where applicable.
Discussion:
A complete analysis of your results (inclusive of your graphs) based on the information learnt
during the study of Rates of Reactions.
Lab 9
Date: 18th March, 2022
Skills assessed: AI
N.B.
The cobalt chloride equilibrium mixture contains concentrated HCl so the person who
will be handling it needs to wear gloves. Be careful when washing the test tubes after
the experiment as well.
AgNO3 decomposes in sunlight, so only collect this solution when you are at test tube
#4.
Background information:
Aims:
0.1M equilibrium mixture of cobalt chloride (~10 ml), 0.1M equilibrium mixture of acidified
potassium chromate (~10ml), AgNO3 solution (10 ml), 6M HNO3 (10 ml) 10% NaOH (10
ml), concentrated HCl (CORROSIVE! - will be administered by teacher), test tubes (8), test
tube rack (2), test tube holder (1), bunsen burner, matches, ice bath, droppers, 50 ml beakers
(5)
Method:
Results:
Discussion:
Key definitions
Explanations for all your observations based on Le Chatelier’s principle (with
relevant equations)
Possible sources of error (explaining their impact on your results)
Conclusion:
Simulation: http://dept.harpercollege.edu/chemistry/chm/100/dgodambe/thedisk/equil/
equil.htm
Lab 10: (To be done in groups of 5)
Date: 25 March, 2022
th
Aim: To describe the trend in solubility and acid/base nature of some of the oxides, chlorides
and hydroxides of period 3 and group 2
Apparatus: 250ml beakers (10), spatula, magnesium oxide, aluminium oxide, silicon dioxide,
calcium oxide, sodium chloride, magnesium chloride, aluminium chloride, sodium hydroxide,
magnesium hydroxide, calcium hydroxide, barium hydroxide, universal pH papers,
thermometer, tap water, top pan balance, weighing paper
Method:
(Wear gloves when handling these hydroxides and avoid contact with your skin)
1. Add approximately 100 ml of distilled water to an empty 250ml beaker
2. Record the temperature of the water
3. Make observations of the solid sodium hydroxide
4. Using the balance, weigh approximately 1 g of sodium hydroxide and add it to the
water in the beaker
5. Stir the solution using the thermometer and record any temperature changes
6. Record observations about the solubility of the oxide
7. Test the pH of the mixture using universal pH paper and record the results
8. Repeat steps 1-7 using magnesium hydroxide, calcium hydroxide and barium
hydroxide.
Results:
Discussion:
Describe and explain the trends in solubility of the oxides, chlorides and hydroxides
of period 3
Describe and explain the trend in the acid/base nature of the oxides, chlorides and
hydroxides of period 3
Describe and explain the trends in solubility of the oxides and hydroxides of Group 2
Describe and explain the trend in the acid/base nature of the oxides and hydroxides of
Group 2
Sources of Error
Conclusion:
Lab 11: Qualitative analysis of halides
Aim: To identify the halide ions by their reactions with concentrated sulphuric acid and
aqueous silver nitrate
Apparatus: test tubes (7), test tube rack (1), 50ml beakers (7), droppers (3), solid samples of
halide salts KX, KY and KZ, distilled water, nitric acid (20 ml), aqueous silver nitrate (10
ml), aqueous ammonia (20 ml), concentrated sulphuric acid (~5 ml) , spatula, test tube
holder, pH paper
Method:
1. Fill 3 beakers with approximately 50ml of distilled water and dissolve a spatula full of
KX, KY and KZ into each beaker.
2. Rinse the four remaining test tubes with soap, followed by distilled water, followed
by a final rinse with nitric acid
3. Add approximately 1ml of distilled water to one of the test tubes. (This will serve as
your control)
4. Add approximately 1 ml of the solution of KX to another test tube
5. Add 5 drops of nitric acid to the test tube and shake to ensure proper mixing
6. Add silver nitrate solution drop-wise to the test tube until a precipitate forms. Shake
the test tube after each drop.
7. Record the color of the precipitate formed
8. Add dilute aqueous ammonia in excess to the test tube noting if any of the precipitate
re-dissolves. Shake the test tube after adding the ammonia.
9. Record your observations.
10. Repeat steps 4-8 using the remaining solutions of KY and KZ
Results:
Discussion:
Identification of the halide ions present with explanations for your deductions
Balanced equations with state symbols for reactions occurring
Identification of products observed when the halides react with concentrates sulphuric
acid
Identification of the type of reaction occurring and identification of what has been
oxidized/reduced where applicable
Conclusion: