Directly related questions
- 17N.3.hl.TZ0.22a.i: Both spectra show a peak at wavenumber 1700 cm–1. Identify the bond responsible for this peak.
- 17N.3.hl.TZ0.22a.i: Both spectra show a peak at wavenumber 1700 cm–1. Identify the bond responsible for this peak.
- 17N.3.hl.TZ0.a.i: Both spectra show a peak at wavenumber 1700 cm–1. Identify the bond responsible for this peak.
- 17N.3.hl.TZ0.27: Ethanol slows down the reaction time of a driver leading to traffic accidents. Explain how the...
- 17N.3.hl.TZ0.27: Ethanol slows down the reaction time of a driver leading to traffic accidents. Explain how the...
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18M.3.hl.TZ1.20b:
Explain how hexane and propanone may be separated by fractional distillation.
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18M.3.hl.TZ1.20b:
Explain how hexane and propanone may be separated by fractional distillation.
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18M.3.hl.TZ1.b:
Explain how hexane and propanone may be separated by fractional distillation.
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18M.3.hl.TZ2.27a:
Fuel cells use an electrochemical process to determine the concentration of ethanol.
Formulate the overall equation for this process.
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18M.3.hl.TZ2.27a:
Fuel cells use an electrochemical process to determine the concentration of ethanol.
Formulate the overall equation for this process.
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18M.3.hl.TZ2.a:
Fuel cells use an electrochemical process to determine the concentration of ethanol.
Formulate the overall equation for this process.
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18N.3.hl.TZ0.23b:
Ethanol in breath can be detected by a redox reaction. Outline this method of detection. An equation is not required.
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18N.3.hl.TZ0.23b:
Ethanol in breath can be detected by a redox reaction. Outline this method of detection. An equation is not required.
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18N.3.hl.TZ0.b:
Ethanol in breath can be detected by a redox reaction. Outline this method of detection. An equation is not required.
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19N.3.hl.TZ0.24c:
Explain how redox chemistry is used to measure the ethanol concentration in a breathalyser.
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19N.3.hl.TZ0.24c:
Explain how redox chemistry is used to measure the ethanol concentration in a breathalyser.
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19N.3.hl.TZ0.c:
Explain how redox chemistry is used to measure the ethanol concentration in a breathalyser.
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17N.3.hl.TZ0.22a.ii:
Deduce which spectrum belongs to paracetamol, giving two reasons for your choice. Use section 26 of the data booklet.
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17N.3.hl.TZ0.22a.ii:
Deduce which spectrum belongs to paracetamol, giving two reasons for your choice. Use section 26 of the data booklet.
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17N.3.hl.TZ0.a.ii:
Deduce which spectrum belongs to paracetamol, giving two reasons for your choice. Use section 26 of the data booklet.
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18M.3.hl.TZ1.20a:
Hexane and propanone have vapour pressures of 17 kPa and 24 kPa respectively at 20 °C.
Calculate the vapour pressure, in kPa, at 20 °C of a mixture containing 60% hexane and 40% propanone by mole fraction, using Raoult’s law and assuming the mixture is ideal.
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18M.3.hl.TZ1.20a:
Hexane and propanone have vapour pressures of 17 kPa and 24 kPa respectively at 20 °C.
Calculate the vapour pressure, in kPa, at 20 °C of a mixture containing 60% hexane and 40% propanone by mole fraction, using Raoult’s law and assuming the mixture is ideal.
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18M.3.hl.TZ1.a:
Hexane and propanone have vapour pressures of 17 kPa and 24 kPa respectively at 20 °C.
Calculate the vapour pressure, in kPa, at 20 °C of a mixture containing 60% hexane and 40% propanone by mole fraction, using Raoult’s law and assuming the mixture is ideal.
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18M.3.hl.TZ2.27b:
Predict the chemical shifts and integration for each signal in the 1H NMR spectrum for ethanol using section 27 of the data booklet.
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18M.3.hl.TZ2.27b:
Predict the chemical shifts and integration for each signal in the 1H NMR spectrum for ethanol using section 27 of the data booklet.
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18M.3.hl.TZ2.b:
Predict the chemical shifts and integration for each signal in the 1H NMR spectrum for ethanol using section 27 of the data booklet.
- 18N.3.hl.TZ0.21c: Explain the process of solvent extraction by which Taxol is isolated.
- 18N.3.hl.TZ0.21c: Explain the process of solvent extraction by which Taxol is isolated.
- 18N.3.hl.TZ0.c: Explain the process of solvent extraction by which Taxol is isolated.
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18N.3.hl.TZ0.23a:
State an analytical technique used to separate anabolic steroids from other compounds in an athlete’s urine or blood.
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18N.3.hl.TZ0.23a:
State an analytical technique used to separate anabolic steroids from other compounds in an athlete’s urine or blood.
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18N.3.hl.TZ0.a:
State an analytical technique used to separate anabolic steroids from other compounds in an athlete’s urine or blood.
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19M.3.hl.TZ1.22a(ii):
The resulting active metabolite of oseltamivir can be detected by mass spectrometry (MS) analysis.
Deduce the mass of the expected carboxylate ion.
Mr oseltamivir = 312
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19M.3.hl.TZ1.22a(ii):
The resulting active metabolite of oseltamivir can be detected by mass spectrometry (MS) analysis.
Deduce the mass of the expected carboxylate ion.
Mr oseltamivir = 312
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19M.3.hl.TZ1.a(ii):
The resulting active metabolite of oseltamivir can be detected by mass spectrometry (MS) analysis.
Deduce the mass of the expected carboxylate ion.
Mr oseltamivir = 312
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19M.3.hl.TZ2.27a:
Describe how a fuel cell breathalyser works.
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19M.3.hl.TZ2.27a:
Describe how a fuel cell breathalyser works.
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19M.3.hl.TZ2.a:
Describe how a fuel cell breathalyser works.
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19M.3.hl.TZ2.27b:
Alcohol levels in the breath can also be determined using IR spectroscopy.
Suggest, giving a reason, which bond’s absorbance is most useful for detecting ethanol in breath.
Bond:
Reason:
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19M.3.hl.TZ2.27b:
Alcohol levels in the breath can also be determined using IR spectroscopy.
Suggest, giving a reason, which bond’s absorbance is most useful for detecting ethanol in breath.
Bond:
Reason:
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19M.3.hl.TZ2.b:
Alcohol levels in the breath can also be determined using IR spectroscopy.
Suggest, giving a reason, which bond’s absorbance is most useful for detecting ethanol in breath.
Bond:
Reason:
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19N.3.hl.TZ0.24a:
Infrared (IR) spectroscopy is used to identify functional groups in organic compounds.
Deduce the wavenumber, in cm−1, of an absorption peak found in the IR spectrum of testosterone but not in that of cholesterol.
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19N.3.hl.TZ0.24a:
Infrared (IR) spectroscopy is used to identify functional groups in organic compounds.
Deduce the wavenumber, in cm−1, of an absorption peak found in the IR spectrum of testosterone but not in that of cholesterol.
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19N.3.hl.TZ0.a:
Infrared (IR) spectroscopy is used to identify functional groups in organic compounds.
Deduce the wavenumber, in cm−1, of an absorption peak found in the IR spectrum of testosterone but not in that of cholesterol.
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19N.3.hl.TZ0.24b:
Describe a technique for the detection of steroids in blood and urine.
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19N.3.hl.TZ0.24b:
Describe a technique for the detection of steroids in blood and urine.
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19N.3.hl.TZ0.b:
Describe a technique for the detection of steroids in blood and urine.
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20N.3.hl.TZ0.15e:
Explain how IR spectroscopy can be used to distinguish aspirin from salicylic acid.
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20N.3.hl.TZ0.15e:
Explain how IR spectroscopy can be used to distinguish aspirin from salicylic acid.
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20N.3.hl.TZ0.e:
Explain how IR spectroscopy can be used to distinguish aspirin from salicylic acid.
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20N.3.hl.TZ0.18a(ii):
The vapour pressure of pure ethanal at is .
Calculate the vapour pressure of ethanal above the liquid mixture at .
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20N.3.hl.TZ0.18a(ii):
The vapour pressure of pure ethanal at is .
Calculate the vapour pressure of ethanal above the liquid mixture at .
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20N.3.hl.TZ0.a(ii):
The vapour pressure of pure ethanal at is .
Calculate the vapour pressure of ethanal above the liquid mixture at .
- 20N.3.hl.TZ0.18b: Describe how this mixture is separated by fractional distillation.
- 20N.3.hl.TZ0.18b: Describe how this mixture is separated by fractional distillation.
- 20N.3.hl.TZ0.b: Describe how this mixture is separated by fractional distillation.