The infrared spectrum of an organic compound is shown.

Which of these compounds would give this infrared spectrum?
Choose your answer
hexanal
hexane
hexanoic acid
hexan-1-ol
9 questions · 11 marks · ≈ 11 min
The infrared spectrum of an organic compound is shown.

Which of these compounds would give this infrared spectrum?
Choose your answer
hexanal
hexane
hexanoic acid
hexan-1-ol
In a mass spectrum, the molecular ion is the ion which always has the
Choose your answer
greatest abundance
greatest stability
highest charge
highest mass/charge ratio
Butan-1-ol and butan-2-ol are isomers.
Which m / z value would be expected to have a significant peak in the mass spectrum of butan-1-ol but not that of butan-2-ol?
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15
29
43
57
Which could be the infrared spectrum of CH2=CHCH2OH?


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An aliphatic organic compound has the infrared spectrum shown.

What are the bond stretches responsible for the peaks P and Q in the spectrum?
| P | Q | ||
|---|---|---|---|
| □ | A | O—H carboxylic acid | C═O carboxylic acid |
| □ | B | O—H carboxylic acid | C═O aldehyde |
| □ | C | C—H aldehyde | C═O carboxylic acid |
| □ | D | C—H aldehyde | C═O aldehyde |
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The infrared spectrum of a compound X is shown.

Which could be compound X?

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The mass spectrum of propanone is shown.

Which fragment is most likely to produce the peak at *m / z *= 43?
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CH3CH2C
CH3CO+
CH2CHO+
CHCH2O+
Which reagent produces a silver mirror when warmed with propanal but not when warmed with propanone?
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2,4-dinitrophenylhydrazine (Brady's reagent)
Acidified potassium dichromate(VI)
Fehling's solution
Tollens' reagent
A colourless liquid, Z, is known to be either ethanol (CH3CH2OH) or methoxymethane (CH3OCH3).
The mass spectrum and infrared spectrum of Z are shown.


What is the relative molecular mass, Mr, of compound Z?
Choose your answer
30
44
46
60
The broad IR absorption in the range 3230–3550 cm–1 is characteristic of which bond?
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C=C
C=O
C–H
O–H (alcohol)
What is the identity of compound Z?
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Ethanol, because the IR shows a broad peak at 3200–3550 cm–1
Ethanol, because the IR shows no peak near 1715 cm–1
Methoxymethane, because both compounds have Mr = 46
Methoxymethane, because methoxymethane contains an O–H bond