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EXPERIMENT 1
Mark Riley
Table A Graph A
Time Temp
(mins) (°C) Temperature vs Time
0.5 22
1 23
70
1.5 23
2 23 60
2.5 23 Series1
3 50
Temperature (°C)
3.5 38 extrapolation
40
4 46
y = -1.0714x + 61.214
4.5 47 30
5 49
5.5 52 20
6 53.5
10
6.5 54
7 54 0
7.5 53 0 1 2 3 4 5 6 7 8 9 10
8 53
8.5 52 Time (mins)
9 51.5
9.5 51
𝑚 4.00
𝑛= = 0.061 𝑚𝑜𝑙𝑒𝑠
𝑁 65.37
25ml of copper(II) sulphate solution containing O.025 moles of copper(II) sulphate was mixed
with 0.061moles(4g) of zinc EX2A. No real care was to be taken in measuring the 4g of zinc as
it is by far the excess reagent. If 1 mole of copper(II) sulphate was used then only one mole of
zinc should be used EX2C because the molar ratio of them in a balanced equation is 1:1 EX2B,
therefore because only 0.025 moles of copper(II) sulphate was used, only 0.025 moles(1.64g)
of zinc is actually needed to be used for a complete reaction EX2E.
The reaction between the zinc and copper(II) sulphate was reasonably fast Graph A causing a
temperature rise of 32°C Table A with the highest temperature being reached within 4
minutes Graph A The energy needed to raise the temperature of 25ml of the solution by 1°c or
K is 3360 Joules EX2F. This energy comes from the difference in the heat content of the
products compared to the reactants. The enthalpy change in this displacement reaction is -
134kJ mol-1 EX2G therefore the reaction was exothermic because heat was given out.
The accepted value for the enthalpy change in this reaction is -219kJ mol-1 which is 39% off
the results achieved through this experiment EX2H. This difference was attributed to the heat
loss to the surroundings during the reaction (proven by extrapolating the trend line back
Graph A), errors or in the measurements (particularly of volume and temperature which was
somewhat caused by limitations in the measuring equipment) and also the concentration of
the copper(II) sulphate solution is assumed not to have been accurately mixed.
Hypothesis: The improvements made to the first experiment will result in a final
enthalpy change that is closer to accepted value.
Procedure: Please see page 6 of the practical manual ATP413 CHEM.2 with the
following modifications
Seal the vessel as best as possible using the lid with a hole to allow
the thermometer access to the solution
Table A Table B
Time Temp
(mins) (°C) Temperature vs Time
0.5 22
60
1 22
1.5 23 55
2 23 50 Series1
Temperature (°C)
2.5 23 45 extrapolation
3
40
3.5 50 Extrapolated
35 Trendline
4 56
30 y = -0.631x + 58.315
4.5 55.5
5 55 25
5.5 54.5 20
6 54.5 0 1 2 3 4 5 6 7 8
6.5 54.5 Time (mins)
7 54
7.5 53.5
𝑚 4.00
𝑛= = 0.061 𝑚𝑜𝑙𝑒𝑠
𝑁 65.37
25ml of copper(II) sulphate solution containing O.025 moles of copper(II) sulphate was again
mixed with 0.061moles(4g) of zinc EX2A but this time the solution was measured using a bulb
pipette instead of a plastic measuring cylinder to improve the accuracy of the measurement.
No efforts were made to improve the accuracy when measuring the 4g of zinc because as
discussed in experiment 1, zinc is by far the excess reagent and only 1.6g is actually needed
EX2D. The vessel which was a polystyrene cup was insulated with layers of aluminum foil to
reduce heat loss to the surroundings. A lid was also placed onto the polystyrene cup to seal the
vessel in a further attempt to contain heat reducing heat loss to the surroundings. Although
these changes did not have a large affect on the overall results, the attempt to contain heat
was somewhat successful as can be seen when comparing Graph A from experiment 1 to
Graph A from experiment 2. Comparing the temperature decrease after the highest
temperature was achieved for both experiments Table A vs Table A proves the effectiveness of
the efforts made to prevent heat loss to the surroundings. More proof of this effectiveness can
be found by comparing the difference between the highest temperature reached to the value
given by extrapolating the trend line back on the graphs for each experiment Graph A Graph A
and comparing the 2 differences (difference is smaller for experiment 2).
The results from the 2nd experiment show a slightly higher temperature change Table A vs
Graph A which resulted in an increased kJ/mol ratio. The percentage error decreased in
comparison to the results from the first experiment EX2G but was still 35% off the published
results EX2H. The explanation for this difference in values remains the same as in the first
experiment even though as explained, changes were made somewhat successfully to this 2nd
experiment to minimize errors.
Conclusion: After accounting for possible errors and making changes in order to maximize
the accuracy, the experiment was repeated and the results showed an enthalpy
change closer to the published value but still significantly lesser. This can be
accounted for by the same reasons as experiment 1.