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Characteristic Organic Reactions

A concise Cambridge International AS Level Chemistry revision guide to the vocabulary of 13.2: nucleophiles and electrophiles, the reaction types addition, substitution, elimination, hydrolysis and condensation, the [O] and [H] convention for organic redox, the four named mechanisms, and the rules for curly arrows.

AS Level
Topic 13: An Introduction to AS Level Organic Chemistry
9701 Papers 1 and 2
Dr. Mohammed Al-Fatah

Written by: Dr. Mohammed Al-Fatah

Chemistry specialist revision notes for A Level Chemistry.

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Before you start

GCSE Recap: Adding Bromine and Making Poly(ethene)

Before you start, check three GCSE ideas that this page turns into named reaction types.

1

Nucleophiles and Electrophiles

Cambridge 13.2.1(e) asks you to interpret and use the terms nucleophile, electrophile, nucleophilic and electrophilic. Both kinds of reagent are defined by what they do with electron pairs.

TermDefinitionWhat it looks forExamples
NucleophileAn electron-pair donor: a species with a lone pair (often negatively charged) that forms a new covalent bond by donating the pairA δ+ atom, usually a carbon bonded to an electronegative atomOH–, CN–, NH3, H2O
ElectrophileAn electron-pair acceptor: a species that is short of electrons and forms a new covalent bond by accepting a pairA region of high electron density, such as a C=C π bondH+, Brδ+ in polarised Br2, NO2+

The adjectives describe the attacking reagent: a nucleophilic reaction is one in which a nucleophile attacks; an electrophilic reaction is one in which an electrophile attacks. A halogenoalkane undergoes nucleophilic substitution because the nucleophile attacks its δ+ carbon; an alkene undergoes electrophilic addition because an electrophile attacks its π bond.

Exam sentence: A nucleophile is an electron-pair donor that attacks an electron-deficient atom; an electrophile is an electron-pair acceptor that attacks a region of high electron density.

Check your understanding

Quick Check: Which Species Are Nucleophiles?

Click every species that can donate a pair of electrons, and leave the acceptors alone.

2

The Five Reaction Types

Cambridge 13.2.1(f) lists five words that describe what happens to the molecule overall. Learn each with a fresh example, then classify any reaction you meet by asking what has been gained, lost or swapped.

Reaction typeWhat happens overallExample equation
AdditionTwo molecules combine to give one; a multiple bond is used upCH3CH=CH2 + HCl → CH3CHClCH3
SubstitutionOne atom or group is replaced by anotherCH3CH2Br + CN– → CH3CH2CN + Br–
EliminationA small molecule is removed from one molecule, creating a multiple bondCH3CH2CH2Br + OH– → CH3CH=CH2 + H2O + Br– (ethanolic KOH, heat)
HydrolysisA bond is broken by reaction with water (or with OH– or H+ in water)CH3COOCH3 + H2O → CH3COOH + CH3OH
CondensationTwo molecules join with the loss of a small molecule, usually waterCH3CH2COOH + CH3OH → CH3CH2COOCH3 + H2O

One example of each Cambridge reaction type, with the part of the molecule that changes highlighted.

Exam focus: Hydrolysis and condensation are opposites: hydrolysis splits a molecule using water; condensation joins two molecules and releases water. Elimination and addition are also opposites.

Check your understanding

Quick Check: Name the Type of Each Reaction

Six reactions, one word each. Ask what has been gained, lost or swapped.

3

Oxidation and Reduction: [O] and [H]

In organic chemistry the oxidising or reducing agent is often complex, so Cambridge 13.2.1(g) allows a shorthand: [O] represents one atom of oxygen supplied by an oxidising agent, and [H] represents one atom of hydrogen supplied by a reducing agent. The equation must still balance.

  • Oxidation: gain of oxygen or loss of hydrogen. Propan-1-ol is oxidised to propanal: CH3CH2CH2OH + [O] → CH3CH2CHO + H2O.
  • Reduction: gain of hydrogen or loss of oxygen. Butanone is reduced to butan-2-ol: CH3COCH2CH3 + 2[H] → CH3CH(OH)CH2CH3.
ChangeClassified asShorthandTypical reagent
Alcohol → aldehyde or ketoneOxidation+ [O], water formedAcidified potassium dichromate(VI)
Aldehyde → carboxylic acidOxidation+ [O]Acidified potassium dichromate(VI), heat under reflux
Aldehyde or ketone → alcoholReduction+ 2[H]NaBH4
Nitrile → amineReduction+ 4[H]LiAlH4 or H2 with a nickel catalyst

Exam sentence: In organic redox equations [O] stands for one oxygen atom from the oxidising agent and [H] for one hydrogen atom from the reducing agent; the equation must balance for every element.

Check your understanding

Quick Check: Balancing [O] and [H]

Type the number of oxygen or hydrogen atoms needed to balance each equation.

4

The Four Named Mechanisms

Cambridge 13.2.2 asks you to understand and use the names of four mechanism types. Each combines a reagent type (radical, electrophile or nucleophile) with an overall reaction type. Knowing the pair tells you which reagent attacks and what the product will be.

MechanismAttacking speciesOverall changeSubstrateMet in
Free-radical substitutionRadical (Cl•, Br•)SubstitutionAlkanesTopic 14.1
Electrophilic additionElectrophile (H+, Brδ+)AdditionAlkenesTopic 14.2
Nucleophilic substitutionNucleophile (OH–, CN–, NH3)SubstitutionHalogenoalkanesTopic 15
Nucleophilic additionNucleophile (CN–, [H] from NaBH4)AdditionAldehydes and ketonesTopic 17

Key idea: Read the name backwards: nucleophilic addition means an addition reaction started by a nucleophile, so look for a δ+ carbon in a C=O bond and a lone-pair reagent.

Check your understanding

Quick Check: More Than One Type

Test the reaction against every definition before you choose.

5

Curly Arrows: The Cambridge Rules

For every mechanism except free-radical substitution, Cambridge expects curly arrows that represent the movement of a pair of electrons. The syllabus note for 13.2.2 gives one rule that examiners apply strictly: the arrow should begin at a bond or a lone pair of electrons. It can end at an atom (forming a bond) or at one atom of a bond that is breaking.

The three places an arrow can start and finish: a lone pair forming a bond, a bond forming another bond, and a bond breaking heterolytically.

  • An arrow from a lone pair to an atom forms a new bond: the nucleophile attacking a δ+ carbon.
  • An arrow from the middle of a bond to an atom outside it forms a new bond: the π bond of an alkene attacking an electrophile.
  • An arrow from the middle of a bond to one of its own atoms breaks the bond heterolytically: the C-Br bond giving Br–.

Exam focus: Radicals are shown with a dot, not with curly arrows. In free-radical substitution write the initiation, propagation and termination equations instead.

Check your understanding

Quick Check: Pick the Accurate Statement

In each round, choose the one statement that is accurate.

6

Common Exam Mistakes

  • Calling OH– an electrophile because it is “reactive”. It donates a lone pair, so it is a nucleophile.
  • Classifying the reaction of an alkene with bromine as substitution. Nothing is replaced; bromine adds across the double bond.
  • Writing [O] without balancing: CH3CH2OH + [O] → CH3CHO needs H2O on the right.
  • Starting a curly arrow on an atom or a charge rather than on a bond or lone pair.
  • Describing hydrolysis as “adding water”. Hydrolysis breaks a bond; addition of water to an alkene is hydration.

Exam sentence: Classify the overall change (addition, substitution, elimination, hydrolysis or condensation), name the attacking species (radical, electrophile or nucleophile), and the mechanism name follows.

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Free Radical Substitution FAQs

These questions summarise the core exam points on alkane substitution and free radicals.

Why are alkanes usually unreactive?

Alkanes are usually unreactive because they contain strong C-C and C-H bonds. These bonds require a large amount of energy to break.

What condition is needed for alkanes to react with chlorine?

Ultraviolet light is needed. UV light provides enough energy to break the Cl-Cl bond by homolytic fission, forming chlorine radicals.

What is a free radical?

A free radical is a species with an unpaired electron. The unpaired electron is usually represented using a dot, such as Cl•.

Why is the reaction called substitution?

It is called substitution because a hydrogen atom in the alkane is replaced by a halogen atom.

Why can a mixture of products form?

After the first substitution, the haloalkane product can undergo further substitution. This can replace more hydrogen atoms and produce a mixture of chlorinated products.

Copyright notice: This OLS revision content, including the explanations, layout, diagrams, tables and embedded learning structure, is authored for Online Learning System by Dr. Mohammed Al-Fatah. It may not be copied, reproduced, redistributed or adapted without written permission.