Syllabus Edition

First teaching 2023

First exams 2025

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Shapes of Aromatic Organic Molecules; σ & π Bonds (CIE A Level Chemistry)

Topic Questions

1a2 marks

This question is about benzene.

Draw the displayed formula for benzene.

1b1 mark

State the bond angle in the planar regular hexagon structure of benzene.

1c1 mark

State the type of hybridisation of the carbon atoms in benzene.

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1a3 marks

Benzene can exist as C6H6 or be substituted in a number of different ways to form aromatic compounds.

State the IUPAC name for compounds W, X and Y


nrhdxjs-_benzene-compounds
1b1 mark

State the IUPAC name for compound Z.

cd80e300-b21c-42e9-991c-55888972d64d
1c1 mark

State the bond angle that is present in the benzene molecule.

1d1 mark

In benzene, each of the carbon atoms is sp2 hybridised.

i)
Explain how neighbouring carbon atoms form σ bonds.

[1]

ii)
Neighbouring carbon atoms also form π bonds. Explain how these π bonds are formed.

[1]

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2a2 marks

State the IUPAC name for the following aromatic compounds

screenshot-2024-03-26-200018

compound X ..........................................................................

compound Y ......................................................................... 

2b2 marks

Explain why the benzene ring is planar.

2c2 marks

Compound Y can be formed from benzene. Outline the reagents for the two step reaction to formation of compound Y


step 1 .......................................................................................


step 2 ......................................................................................

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3a1 mark

State the bond angle that is present in the benzene molecule.

3b5 marks

Explain why a molecule of benzene, C6H6 does not tend to react with bromine whereas hexene, C6H12, will react to form dibromohexane, C6H12Br2

3c1 mark

State the name of the mechanism that benzene will undergo if reacted with bromine in the presence of a halogen carrier to form bromobenzene, C6H5Br.   

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