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Reactions

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

What is the main reaction that alkenes undergo?

Back (Answer)

Addition reactions

#2
Front (Question)

What is the addition reaction of alkenes more often called?

Back (Answer)

Halogenation

#3
Front (Question)

Give two examples of halogens that alkenes react readily with during halogenation.

Back (Answer)

Cl2 Br2

#4
Front (Question)

What is formed from the halogenation of an alkene?

Back (Answer)

A halo-alkane e.g. 2,3-dichlorobutane

#5
Front (Question)

What is needed for halogenation?

Back (Answer)

An alkene A halogen molecule No light or heat is necessary - reaction occurs on its own

#6
Front (Question)

How does the halogenation of alkanes differ from the halogenation of alkenes?

Back (Answer)

Alkanes require light or heat to become halogenated

#7
Front (Question)

What reaction prepares alkynes?

Back (Answer)

Elimination reactions

#8
Front (Question)

How are alkynes prepared by an elimination reaction? 3

Back (Answer)

A strong base removes the hydrogens and halogens from either vicinal or germinal dihalides This forms an alkyne Done through two successive elimination reactions

#9
Front (Question)

How can alkenes be made into alkynes? 3

Back (Answer)

Two step process Halogenation of the alkene Double dehydrohalogenation of the resulting vicinal dihalide

#10
Front (Question)

From what two families can alcohols be formed?

Back (Answer)

Alkenes or alkyl halides

#11
Front (Question)

How can alcohols be formed from alkenes? 5

Back (Answer)

Addition reaction of a water molecule to an alkene in the presence of an acid Acid donates a hydrogen to break the double bond Water bonds to molecule Deprotonation then occurs OH of water forms the hydroxyl group

#12
Front (Question)

How can alcohols be formed from alkyl halides? 3

Back (Answer)

By the loss of a leaving group (halogen) Water molecule then binds to molecule Deprotonation then occurs to rid the H2O of one H leaving an OH group

#13
Front (Question)

How are ethers synthesised?

Back (Answer)

A substitution reaction by reacting alkyl halides with an alkoxide ion

#14
Front (Question)

What is an alkoxide ion?

Back (Answer)

Conjugate base of alcohol i.e. alcohol without a H

#15
Front (Question)

What is the synthesis of ethers called?

Back (Answer)

The Williamson Ether synthesis

#16
Front (Question)

Give an example of an alkoxide ion used in ether synthesis/

Back (Answer)

sodium alkoxide

#17
Front (Question)

How does the synthesis of ethers work? 3

Back (Answer)

Sodium alkoxide reacts with an alkyl halide containing chlorine Alkoxide acts as a neutrophil Alkyl halide acts as an electrophile Form an ether and NaCl

#18
Front (Question)

What happens when you oxidise a primary alcoho using a weak oxidantl?

Back (Answer)

It forms and aldehyde

#19
Front (Question)

When happens when you oxidise a primary alcohol with a strong oxidant?

Back (Answer)

Forms and aldehyde then a carboxylic acid

#20
Front (Question)

What is formed when you oxidise a secondary alcohol?

Back (Answer)

It forms a ketone

#21
Front (Question)

Whats formed when you reduce an aldehyde?

Back (Answer)

It forms a primary alcohol

#22
Front (Question)

What happens when you reduce a carboxylic acid?

Back (Answer)

It forms an aldehyde

#23
Front (Question)

Whats formed when you reduce a ketone?

Back (Answer)

Secondary alcohol

#24
Front (Question)

Define a substitution reaction

Back (Answer)

A substitution reaction is a chemical reaction during which one functional group in a chemical compound is replaced by another functional group