Chloroethane and chlorobenzene both contain a chlorine atom bonded to a carbon atom. Explain why chloroethane reacts readily with aqueous sodium hydroxide, whereas chlorobenzene does not react with aqueous sodium hydroxide under the same conditions.
CAIE A Level Chemistry 9701 · Halogen compounds
Halogen compounds: explain question
Explain4 marksStandard
How this question is marked
4 marks, so the mark scheme is looking for about 4 separate creditworthy points. Making the same point twice in different words earns it once.
Explain means: Give the reasons or the mechanism: why or how something happens. Link each point to the next with because, so or which means. A list of facts with no links usually loses the reasoning marks.
More Halogen compounds questions
- 4 marks · Explain why primary halogenoalkanes tend to undergo nucleophilic substitution via an SN2 mechanism, whereas tertiary halogenoalkanes tend…
- 5 marks · Chloroethane and chlorobenzene are both halogeno compounds. A student adds aqueous silver nitrate to separate samples of each compound and…
- 6 marks · Chloroethane reacts readily with aqueous sodium hydroxide to form ethanol. Chlorobenzene does not react with aqueous sodium hydroxide…
- 5 marks · 2-bromo-2-methylpropane reacts with aqueous sodium hydroxide to form 2-methylpropan-2-ol. Explain the mechanism of this reaction…
- 6 marks · A student plans to prepare chlorobenzene from benzene and then compare its reactivity with chloroethane. (a) Describe how the student…
- 7 marks · 2-bromo-2-methylpropane, (CH3)3CBr, is a tertiary halogenoalkane. A student adds a few drops of aqueous silver nitrate, AgNO3(aq), in…
Written by Markquill to follow the Cambridge International syllabus. Markquill is independent and is not affiliated with or endorsed by Cambridge International.