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Chapter 13 - Alkenes

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Total cards: 19•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

What is a polymer

Back (Answer)

A polymer consists of many repeat units (monomers) joined together to make a long chain

#2
Front (Question)

How do alkenes form long saturated polymer chains

Back (Answer)

They undergo addition polymerisation

#3
Front (Question)

What are some uses for Polythene

Back (Answer)

Shopping bags

#4
Front (Question)

What are some uses for Polychloroethene and what is it more commonly known as

Back (Answer)

PVC * Pipes * Floor tiles

#5
Front (Question)

What are some uses for Polypropene

Back (Answer)

• Crates • Ropes

#6
Front (Question)

What are some uses for

Back (Answer)

#7
Front (Question)

What are some uses for Polytetrafluoroethene PTFE

Back (Answer)

Non-stick pans

#8
Front (Question)

What are problems with recycling polymers

Back (Answer)

Costly to sort by hand Mixed polymers renders the product unusable PVC recycling - Releases toxic hydrogen chloride and dioxins when burnt

#9
Front (Question)

What are positive aspects to recycling polymers

Back (Answer)

• Conserves finite fossil fuels and decreases amount of waste going into landfill • Waste polymers can be incinerated to produce heat, generating steam to power turbines producing electricity • Reclaiming monomers from waste polymers which can be used as raw materials for the production of new polymers

#10
Front (Question)

What are biodegradable polymers

Back (Answer)

Polymers that are broken down by bacteria into water, carbon dioxide, and biological compounds

#11
Front (Question)

What are photodegradable polymers

Back (Answer)

Polymers containing bonds weakened by absorbing light

#12
Front (Question)

What is Markownikoff’s rule

Back (Answer)

The stability of the carbocation intermediate increases the more alkyl groups there are attached to the positively charged carbon atom

#13
Front (Question)

Why are alkenes much more reactive than alkanes

Back (Answer)

• The π-electrons are more exposed than the σ-electrons as they are on the outside of the double bond • The π-bond readily breaks and alkenes undergo addition reactions relatively easily

#14
Front (Question)

What conditions are required for hydrogenation of alkenes

Back (Answer)

Nickel Catalyst

#15
Front (Question)

What conditions are required for the halogenation of alkenes

Back (Answer)

React with Chlorine and Bromine at room temperature

#16
Front (Question)

What conditions are required for alkenes to react with hydrogen halides

Back (Answer)

Room Temperature

#17
Front (Question)

What conditions are required for the hydration of Alkenes

Back (Answer)

Steam Phosphoric acid Catalyst

#18
Front (Question)

How do you test for the presence of a C=C double bond and what is the change

Back (Answer)

• Add bromine water • The orange colour goes colourless

#19
Front (Question)

What is Cis-Trans isomerism

Back (Answer)

• Must have a C=C double bond • Two different groups must be attached to each carbon of the double bond • One of the attached groups on each carbon must be the same