1.Use the recorded data to fill in the blanks. Show work for calculations.
Trial 1 |
Trial 2 |
Trial 3 |
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a |
Initial temperature of the cold water in the calorimeter (°C): |
21.5 |
21.5 |
21.5 |
b |
Initial temperature of the hot water (°C): |
60.0 |
60.0 |
60.0 |
c |
Mass of the hot water (assume density of 1.00 g/mL) (g) |
50.0g |
50.0g |
50.0g |
d |
Mass of the cold water (assume density of 1.00 g/mL) (g) |
50.0g |
50.0g |
50.0g |
e |
Final (maximum) temperature of water mixture the calorimeter (°C): |
39.8 |
39.8 |
39.8 |
f |
Calculate change in Temperature, DThot water (Tfinal – Tinitial hot) |
-10.2 |
-10.2 |
-10.2 |
g |
Calculate change in temperature, DTcold water (Tfinal – Tinitial cold) |
18.3 |
18.3 |
18.3 |
h |
Calculate qhot (J) |
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j |
Calculate qcold (J) |
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k |
Calculate qcalorimeter (J) |
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l |
Calculate Heat Capacity of Calorimeter, Cp(J/°C) |
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Average Heat Capacity of Calorimeter, Cp, J/°C) |
In another industrial lab, the heat capacity of the calorimeter was measured by a more precise method, and was determined to be 21.3 J/°C. Note because Cp values are so small, your experimental value may deviate largely (up to about 30% error) from the industrial value determined with more precise equipment. Use this industrial value (theoretical value) and the average Cp value you obtained in Experiment 1 (experimental value) to determine the percent error in your experimental value.:
Calculate change in Temperature, DThot water = (Tfinal – Tinitial hot) = 39.8 - 60 = -20.2
qhot = m x c x (DT)hot water
qhot = 50 x 4.18 x (-20.2)
qhot = -4221.8 J
qcold = m x c x (DT)cold water
qcold = 50 x 4.18 x (18.3)
qcold = 3824.7 J
Heat lost by hot water = heat gained by calorimeter + heat gained by cold water
qhot = qcalorimeter + qcold
qcalorimeter = qhot - qcold
qcalorimeter =4221.8 -3824.7 = 397.1 J
qcalorimeter = 397.1 J
Calorimeter contains cold water
so specific heat of calorimeter =
c=397.1/18.3 = 21.7 J/oC
specific heat of calorimeter = 21.7 J/oC
percentage error =
percentage error =
percentage error = 1.9%
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