The delocalised electrons in benzene result from the overlap of
s orbitals to form σ bonds
s orbitals to form bonds
p orbitals to form σ bonds
p orbitals to form bonds
Did this page help you?
Select a question set to download for
5.4 Organic Chemistry: Arenes
Select an answer set to view for
5.4 Organic Chemistry: Arenes
The delocalised electrons in benzene result from the overlap of
s orbitals to form σ bonds
s orbitals to form bonds
p orbitals to form σ bonds
p orbitals to form bonds
Choose your answer
Did this page help you?
Methylbenzene reacts with a mixture of concentrated nitric acid and concentrated sulfuric acid to form 2,4,6‐ trinitromethylbenzene.
seven
six
five
four
Choose your answer
nucleophilic addition
nucleophilic substitution
electrophilic addition
electrophilic substitution
Choose your answer
Which expression shows the mass in grams of 2,4,6‐trinitromethylbenzene formed from 10 g of methylbenzene if the yield of the reaction is 85%?
[Mr values: methylbenzene = 92 2,4,6‐trinitromethylbenzene = 227]
(10 × 85 × 227) ÷ (92 × 100)
(10 × 100 × 227) ÷ (92 × 85)
(10 × 100 × 227) ÷ (92 × 115)
(10 × 115 × 227) ÷ (92 × 100)
Choose your answer
Did this page help you?
Benzene is sometimes represented by a Kekulé structure.
If this were the only structure of benzene, what would be the total number of isomers of dichlorobenzene?
two
three
four
five
Choose your answer
Did this page help you?
What is the product when benzene reacts with fuming sulfuric acid?
Choose your answer
Did this page help you?
Which of these could not be formed when excess benzene is heated with trichloromethane, CHCl3, in the presence of an aluminium chloride catalyst?
Choose your answer
Did this page help you?
Hydrogen bonds are formed when methylamine dissolves in water.
Which structure best represents a hydrogen bond between methylamine and water?
Choose your answer
Did this page help you?
What is the molar mass, in g mol–1, of the organic product when phenol reacts with excess bromine water?
156.9
172.9
330.7
488.5
Choose your answer
Did this page help you?
The reaction of ethene with bromine occurs under normal laboratory conditions but the reaction of benzene with bromine to form bromobenzene requires heat and the presence of a catalyst.
The best explanation for the difference in reactivity is that the delocalised electrons in benzene
repel electrophiles
result in a kinetic barrier to intermediate formation
result in benzene having an endothermic enthalpy of formation
make benzene thermodynamically stable with respect to the formation of bromobenzene
Choose your answer
Did this page help you?