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Edexcel A Level Chemistry

Halogenoalkanes

Halogenoalkanes have a polar carbon–halogen bond that nucleophiles attack.

Exam Papers
Paper 2
9CH0/02
Specification Points
6.5 – 6.36
10 points covered
Sub-topics
5 lessons
Revision notes available
Exam Board
Edexcel
Pearson 9CH0

Revision Notes

Work through each part of Edexcel Topic 6 in a structured sequence.

Reaction Memory Game

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Halogenoalkanes
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Reaction memory game: Halogenoalkanes

Turn the cards over two at a time: match reagents to what they make, and find how each product is made.

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A free memory game on the reactions in this topic, with your board's reagents, conditions and spec points.

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Synthesis maps

Download, print and revise the reactions of this topic at a glance.

Synthesis map · PDF

Halogenoalkanes Map

Edexcel A Level Chemistry · Topic 6D Halogenoalkanes

Every reaction on one A4 page: reagents, conditions and reaction type for each arrow, colour coded, with the key tests.

Download the map7 reactions · A4 landscape · print ready
Summary map · PDF

Halogenoalkanes Summary Map

Edexcel A Level Chemistry · Topic 6 Organic Chemistry I · 6D Halogenoalkanes

The whole section on one A4 page: reaction types and nucleophiles, names and classes, substitution by hydroxide, water, ammonia and cyanide, elimination, and rates of hydrolysis.

Download the map6 key ideas + a data table · A4 portrait · print ready

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Specification Coverage

Halogenoalkanes – Edexcel A Level Chemistry

The following specification points outline the knowledge and skills students are expected to demonstrate for Topic 6.

6A: Introduction to organic chemistry

6.5
be able to classify reactions as addition, elimination, substitution, oxidation, reduction, hydrolysis or polymerisation

6C: Alkenes

6.21
know what is meant by the term electrophile
6.23
understand that heterolytic bond fission of a covalent bond results in the formation of ions

6D: Halogenoalkanes

6.30
know that halogenoalkanes can be classified as primary, secondary or tertiary
6.31
understand what is meant by the term nucleophile
6.32
understand the reactions of halogenoalkanes with:
i
aqueous potassium hydroxide to produce alcohols, where the hydroxide ion acts as a nucleophile
ii
aqueous silver nitrate in ethanol, where water acts as a nucleophile
iii
potassium cyanide to produce nitriles, where the cyanide ion acts as a nucleophile
iv
ammonia to produce primary amines, where the ammonia molecule acts as a nucleophile
v
ethanolic potassium hydroxide to produce alkenes, where the hydroxide ion acts as a base
6.33
understand that experimental observations and data can be used to compare the relative rates of hydrolysis of primary, secondary and tertiary halogenoalkanes, and chloro-, bromo-, and iodoalkanes, using aqueous silver nitrate in ethanol. Core Practical 4: Investigation of the rates of hydrolysis of some halogenoalkanes.
6.34
know the trend in reactivity of primary, secondary and tertiary halogenoalkanes
6.35
understand, in terms of bond enthalpy, the trend in reactivity of chloro-, bromo-, and iodoalkanes
6.36
understand the mechanisms of the nucleophilic substitution reactions between primary halogenoalkanes and aqueous potassium hydroxide, and ammonia
Specification Coverage

Halogenoalkanes – Edexcel A Level Chemistry

The following specification points outline the knowledge and skills students are expected to demonstrate for Topic 6.

6A: Introduction to organic chemistry

6.5
be able to classify reactions as addition, elimination, substitution, oxidation, reduction, hydrolysis or polymerisation

6C: Alkenes

6.21
know what is meant by the term electrophile
6.23
understand that heterolytic bond fission of a covalent bond results in the formation of ions

6D: Halogenoalkanes

6.30
know that halogenoalkanes can be classified as primary, secondary or tertiary
6.31
understand what is meant by the term nucleophile
6.32
understand the reactions of halogenoalkanes with:
i
aqueous potassium hydroxide to produce alcohols, where the hydroxide ion acts as a nucleophile
ii
aqueous silver nitrate in ethanol, where water acts as a nucleophile
iii
potassium cyanide to produce nitriles, where the cyanide ion acts as a nucleophile
iv
ammonia to produce primary amines, where the ammonia molecule acts as a nucleophile
v
ethanolic potassium hydroxide to produce alkenes, where the hydroxide ion acts as a base
6.33
understand that experimental observations and data can be used to compare the relative rates of hydrolysis of primary, secondary and tertiary halogenoalkanes, and chloro-, bromo-, and iodoalkanes, using aqueous silver nitrate in ethanol. Core Practical 4: Investigation of the rates of hydrolysis of some halogenoalkanes.
6.34
know the trend in reactivity of primary, secondary and tertiary halogenoalkanes
6.35
understand, in terms of bond enthalpy, the trend in reactivity of chloro-, bromo-, and iodoalkanes
6.36
understand the mechanisms of the nucleophilic substitution reactions between primary halogenoalkanes and aqueous potassium hydroxide, and ammonia