Lesson 19B.1
19B.1 13C and 1H NMR spectroscopy Quiz: Pearson Edexcel Chemistry, Unit 19
20 questions
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Lesson 19B.1, 13C and 1H NMR spectroscopy: 20 multiple choice questions for the Pearson Edexcel Chemistry (9CH0), Unit 19: Modern Analytical Techniques II, written with Revision Ninja.
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The 20 questions
-
How many 13C NMR peaks does propanone, CH3COCH3, show?
- 1
- 3
- 2
- 6
-
How many 13C NMR peaks does ethanol show?
- 2
- 3
- 4
- 1
-
How many 13C NMR peaks does butan-2-one, CH3COCH2CH3, show?
- 5
- 4
- 3
- 2
-
What is the typical 13C chemical shift range of a ketone carbonyl carbon?
- About 10-50 ppm
- About 110-160 ppm
- About 50-90 ppm
- About 200-220 ppm
-
What is the typical 13C chemical shift range of an aromatic carbon?
- About 200-220 ppm
- About 110-160 ppm
- About 170-185 ppm
- About 10-50 ppm
-
What reference compound sets 0 ppm in NMR spectra?
- Chloroform, at 7.3 ppm
- Tetramethylsilane (TMS)
- Sodium chloride, at 100 ppm
- Water, at 4.7 ppm
-
What is the typical 1H chemical shift of an aldehyde proton?
- 2-3 ppm
- 4-5 ppm
- 7-8 ppm
- 9-10 ppm
-
What is the typical 1H chemical shift of protons on a carbon bonded to an oxygen atom, such as the CH2 in ethanol?
- 5.0-6.0 ppm
- 3.5-4.5 ppm
- 10-12 ppm
- 0.5-1.5 ppm
-
In the 1H NMR spectrum of ethanol, what is the ratio of peak areas for CH3 : CH2 : OH?
- 2:3:1
- 1:2:3
- 3:1:2
- 3:2:1
-
What splitting pattern is seen for a CH2 group adjacent to a CH3 group?
- A doublet
- A triplet
- A quartet
- A singlet
-
What splitting pattern is seen for a CH3 group adjacent to a CH2 group?
- A singlet
- A quartet
- A triplet
- A doublet
-
What splitting pattern is seen for a CH3 group with no adjacent hydrogen atoms?
- A quartet
- A triplet
- A singlet
- A doublet
-
A 1H NMR spectrum shows a singlet at 2.1 ppm (3H) and a singlet at 3.7 ppm (3H). Which compound fits?
- Propanone, CH3COCH3
- Ethyl methanoate, HCOOCH2CH3
- Methyl ethanoate, CH3COOCH3
- Propanal, CH3CH2CHO
-
How many 1H environments does ethanal, CH3CHO, have?
- 2
- 4
- 1
- 3
-
How many 1H environments does propan-2-ol have?
- 2
- 4
- 5
- 3
-
A 1H NMR spectrum of an aromatic compound shows a peak near 7.2 ppm integrating to 5H. What does this suggest?
- A carboxylic acid group, which gives a broad peak near 11 ppm for the acid proton
- An aldehyde group, which gives a strong peak near 9.8 ppm in the spectrum
- A terminal alkene with a CH2 group, which absorbs strongly near 5 ppm
- A monosubstituted benzene ring
-
A spectrum shows a doublet at 1.2 ppm (6H), a septet at 4.0 ppm (1H) and an OH peak at 2.0 ppm (1H). Which compound fits?
- Propanal
- Propanone
- Propan-1-ol
- Propan-2-ol
-
How many 13C environments does p-xylene (1,4-dimethylbenzene) have?
- 4
- 3
- 6
- 2
-
Which typical 1H chemical shift range is expected for a proton on a C=C in an alkene?
- 11-12 ppm
- 0.8-1.5 ppm
- 4.5-6.5 ppm
- 9.5-10.5 ppm
-
Which typical 1H chemical shift range is expected for a carboxylic acid OH proton?
- 6-7 ppm
- 2-3 ppm
- 0-1 ppm
- 10-12 ppm
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