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Alkenes

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

Card preview (24)

#1
Front (Question)

What is an alkene

Back (Answer)

An unsaturated hydrocarbon

#2
Front (Question)

What is the general formula for alkenes

Back (Answer)

CₙH₂ₙ

#3
Front (Question)

What mechanism can alkenes undergo when they react with an electrophile

Back (Answer)

Electrophilic addition

#4
Front (Question)

Why are alkenes attacked by electrophiles

Back (Answer)

They contain a double bond with a high electron density

#5
Front (Question)

What is an electrophile

Back (Answer)

An electron pair acceptor They are deficient in electrons and are therefore attracted to the double bond in alkenes

#6
Front (Question)

Give two categories which can be electrophiles

Back (Answer)

Positively charged ions Polar molecules

#7
Front (Question)

What is the test for alkenes

Back (Answer)

When we add bromine water, if alkenes are present, a colour change will occur from brown/orange to colourless

#8
Front (Question)

What do we form when we add bromine to an alkene

Back (Answer)

A dibromoalkane

#9
Front (Question)

By what mechanism does bromine react with an alkene

Back (Answer)

Electrophilic addition

#10
Front (Question)

Draw the mechanism for the reaction between bromine and ethene

Back (Answer)

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#11
Front (Question)

Explain how Br2 is polar when reacting with an alkene

Back (Answer)

When a bromine molecule approaches the double bond in an alkene, the electrons in the nearest Br atom repel the high electron density in the double bond, causing a temporary induced dipole, and the nearest bromine atom to be be delta positive, and the bromine molecule to be polar

Card back image
#12
Front (Question)

What is the intermediate called which is formed when bromine reacts with an alkene

Back (Answer)

A carbocation

#13
Front (Question)

What colour are dibromoalkanes

Back (Answer)

Colourless

#14
Front (Question)

What is formed when an alkene reacts with a hydrogen halide

Back (Answer)

Halogenoalkanes

#15
Front (Question)

Draw the mechanism for the reaction between hydrogen bromide and ethene

Back (Answer)

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#16
Front (Question)

How many products do we form when a hydrogen halide reacts with an unsymmetrical alkene

Back (Answer)

2 (Due to ability for different carbocations to form)

#17
Front (Question)

What is the amount of a specific product that is produced dependent on when an unsymmetrical alkene reacts with a hydrogen halide

Back (Answer)

The stability of the carbocation intermediate

#18
Front (Question)

What determines the stability of a carbocation and explain why this is the case

Back (Answer)

The number of alkyl groups bonded to the positive carbon The more alkyl groups bonded, the more stable the carbocation is This is because alkyl groups push electrons towards the positive carbon stabilising it

#19
Front (Question)

What is a primary, secondary and tertiary carbocation

Back (Answer)

Primary - 1 alkyl group bonded to the positive carbon Secondary - 2 alkyl groups bonded to the positive carbon Tertiary - 3 alkyl groups bonded to the positive carbon

Card back image
#20
Front (Question)

What do we call the product formed from a less stable carbocation when an unsymmetrical alkene reacts with a hydrogen halide

Back (Answer)

Minor product

#21
Front (Question)

What do we call the product formed from a more stable carbocation when an unsymmetrical alkene reacts with a hydrogen halide

Back (Answer)

Major product

#22
Front (Question)

Draw the mechanism for the reaction between prop-1-ene and hydrogen bromide. Identify which is the major product

Back (Answer)

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#23
Front (Question)

What are the conditions for the reaction of bromine with an alkene

Back (Answer)

Room temperature (not in UV light)

#24
Front (Question)

What are the conditions for the reaction of hydrogen halides with an alkene

Back (Answer)

Room temperature