Syllabus Edition

First teaching 2023

First exams 2025

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Characteristic Organic Reactions (AL) (CIE A Level Chemistry)

Exam Questions

37 mins4 questions
1a3 marks

This question is about benzene.

i)
Explain why the benzene molecule is planar.

[2]

ii)
Explain why all of the carbon-carbon bonds in benzene are the same length.

[1]

1b3 marks

Benzene can be nitrated by warming it with a mixture of concentrated sulfuric acid and concentrated nitric acid.

The mechanism for the reaction is shown in Fig. 1.1.

7-1-3b-m-nitration-mechanism
Fig. 1.1


Name the type of mechanism of this nitration reaction. Explain your answer.

1c2 marks

Benzene can be used to synthesise (4-aminophenyl)ethanoic acid which is a drug that can be used to treat chronic inflammation of the intestines.

i)
Draw the structural formula of (4-aminophenyl)ethanoic acid.

[1]

ii)
One of the intermediate products made during the synthesis of (4-aminophenyl)ethanoic acid is the molecule shown in Fig. 1.2.
7-1-3c-m-4-nitromethylbenzene-a

Fig. 1.2

Give the IUPAC name of the molecule shown in Fig. 1.2.

[1]

1d3 marks

Noradrenaline, shown in Fig. 1.3, is a hormone and neurotransmitter which contains a benzene ring. It is released during stress to stimulate the heart and increase blood pressure.

7-1-3d-m-noradrenaline

Fig. 1.3

Other than the arene functional group, state the name of three functional groups in the noradrenaline molecule.

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2a4 marks

Benzene, C6H6, typically undergoes electrophilic substitution

i)
State the meaning of the term electrophile.
[1]
ii)
Write an equation for the reaction between benzene and concentrated nitric acid.
[1]
iii)
Identify the electrophile in the reaction and show, by means of an equation, how it is generated.
[2]
2b5 marks

Benzene is a highly unsaturated molecule.

i)
Discuss why benzene undergoes substitution reactions rather than addition reactions.
[3]
ii)
Show, by means of an equation, the reaction of benzene with chlorine and state any necessary conditions.
[2]
2c3 marks

An aromatic organic compound with molecular formula C7H8 reacts with bromine in the presence of UV light to produce a compound with molecular formula C7H7

i)
Name the type of reaction taking place.
[1]
ii)
Deduce the structures of the reactant and product.
[1]
iii)
Give the formula of an additional organic product that could be obtained in the reaction.
[1]

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3a1 mark

Propanal reacts with potassium cyanide, followed by dilute acid, to form the hydroxynitrile CH3CH2CH(OH)CN.

Give the IUPAC name of CH3CH2CH(OH)CN. 

3b1 mark

Name the mechanism for the reaction between potassium cyanide and propanal.

3c2 marks

Explain why propanal is likely to undergo this mechanism.

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1a5 marks

Under suitable conditions, 3-nitrobenzaldehyde can be formed by the reaction of benzaldehyde with appropriate reagents. 

i)
Give the mechanism, reagents and conditions for the formation of 3-nitrobenzaldehyde.
 
mechanism ................................................................................
 
reagents ................................................................................
 
conditions ................................................................................
 
[3]
 
ii)
Draw the fully displayed formula of 3-nitrobenzaldehyde highlighting the functional groups.
 
[2]
1b3 marks

Benzaldehyde, C6H5CHO, is the simplest aromatic aldehyde with a characteristic smell of almonds or cherries.

i)
Give the bond angles within a molecule of benzaldehyde. Explain your answer.
 
[1]
 
ii)
Explain why a molecule of benzaldehyde may not be planar.
 
[2]
1c2 marks

Benzaldehyde reacts with ethanoyl bromide in the presence of a suitable catalyst.

i)
Using the information in part (b), draw the structure of the organic product of this reaction. 
 
[1]
 
ii)
Identify the number of sigma and pi bonds in the organic product.
 
sigma bonds ..............................
 
pi bonds ..............................
 
[1]

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