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Candidate A...Advanced Higher Chemistry Project 2019 - Data Analysis Candidate evidence SQA | 2 of...

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Candidate A Results Repeats Replicate 1 Replicate 2 Control using butanone Physical properties Colour clear, colourless clear, colourless clear, colourless State at 25 °C liquid liquid liquid Smell solvent smell solvent smell solvent smell pH 7 7 7 Saturation Saturated Saturated Saturated Polarity Immiscible in water Immiscible in water Immiscible in water Flammability burns with clear flame, vapour flammable burns with clear flame, vapour flammable burns with clear flame, vapour flammable Density: Mass of beaker (g) 1 55.3662 52.3475 52.2249 2 55.3623 52.3212 52.2753 3 55.3765 52.3560 52.2249 Mass of beaker and 50ml of organic compound (g) 1 95.4832 92.4396 92.2318 2 95.5323 92.3129 92.3249 3 95.4832 92.4612 92.2138 Difference in mass (g) 1 40.1170 40.0921 40.0069 2 40.1700 39.9917 40.0496 3 40.1067 40.1052 39.9889 Density (mass/volume (0.05l)) (kg/m³) 1 802.3 801.8 800.1 2 803.4 799.8 801.0 3 802.1 802.1 799.8 Average 802.6 801.3 800.3 Chemical tests Reaction with sodium metal no reaction no reaction no reaction Reaction with Tollens’ solution Silver mirror forms Silver mirror forms Silver mirror forms Melting point of crude derivative (°C) 115 114 114 Melting point of purified derivative (°C) 1 116 115 117 2 116 117 116 3 115 117 115 Average 115.7 116.3 116.0 Advanced Higher Chemistry Project 2019 - Data Analysis Candidate evidence SQA | www.understandingstandards.org.uk 1 of 15
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Page 1: Candidate A...Advanced Higher Chemistry Project 2019 - Data Analysis Candidate evidence SQA | 2 of 15 Candidate B Advanced Higher Chemistry Project 2019 - Data Analysis Candidate evidence

Candidate A

Results

Repeats Replicate 1 Replicate 2 Control using butanone

Phys

ical

pro

perti

es

Colour clear, colourless

clear, colourless

clear, colourless

State at 25 °C liquid liquid liquid Smell solvent smell solvent smell solvent

smell pH 7 7 7 Saturation Saturated Saturated Saturated Polarity Immiscible in

water Immiscible in water

Immiscible in water

Flammability burns with clear flame, vapour flammable

burns with clear flame, vapour flammable

burns with clear flame, vapour flammable

Density:

Mass of beaker (g) 1 55.3662 52.3475 52.2249 2 55.3623 52.3212 52.2753 3 55.3765 52.3560 52.2249

Mass of beaker and 50ml of organic compound (g)

1 95.4832 92.4396 92.2318 2 95.5323 92.3129 92.3249 3 95.4832 92.4612 92.2138

Difference in mass (g) 1 40.1170 40.0921 40.0069 2 40.1700 39.9917 40.0496 3 40.1067 40.1052 39.9889

Density (mass/volume (0.05l)) (kg/m³)

1 802.3 801.8 800.1 2 803.4 799.8 801.0 3 802.1 802.1 799.8 Average 802.6 801.3 800.3

Che

mic

al te

sts

Reaction with sodium metal

no reaction no reaction no reaction

Reaction with Tollens’ solution

Silver mirror forms

Silver mirror forms

Silver mirror forms

Melting point of crude derivative (°C)

115 114 114

Melting point of purified derivative (°C)

1 116 115 117 2 116 117 116 3 115 117 115 Average 115.7 116.3 116.0

Advanced Higher Chemistry Project 2019 - Data Analysis Candidate evidence

SQA | www.understandingstandards.org.uk 1 of 15

Page 2: Candidate A...Advanced Higher Chemistry Project 2019 - Data Analysis Candidate evidence SQA | 2 of 15 Candidate B Advanced Higher Chemistry Project 2019 - Data Analysis Candidate evidence

Density Calculations: The mass of the compound was found using weighing by difference. The mass of the empty beaker was taken away from the mass of the beaker containing the compound to find the mass of the compound. Then the density was calculated by dividing the mass by the volume of the compound. Example calculation using data from the 1st repeat of 1st replicate: Mass of beaker and compound – Mass of beaker = Mass of compound 95.4832 g - 55.3662 g = 40.1170g Mass of compound ÷ Volume of compound = Density 40.1170 g ÷ 0.05000 m3 = 802.3 kg/m3 IR Spectra

Identified groups: [6] Peak around 2950 cm-1 = C-H stretch Peak around 1700 cm-1 = C=O stretch Peak around 1390 cm-1 = C-H bend The top spectra shown is for the unknown organic compound. Using the software package on the PC, the school’s IR library was searched. This provided a 99.75% match with the spectra for “ethyl methyl ketone” or butanone (shown below)

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Candidate B

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Candidate C

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Candidate D

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Candidate E

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Candidate F

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