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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)

general formula of alkenes

Back (Answer)

CnH2n

#2
Front (Question)

how do pi bonds form

Back (Answer)

sideways double overlap of 2p orbitals above and below the plane

#3
Front (Question)

what is the shape of alkenes?

Back (Answer)

trigonal planar

#4
Front (Question)

what is the bond angle of alkenes?

Back (Answer)

120

#5
Front (Question)

stereoisomers definition

Back (Answer)

same structural formula but a different arrangement of the atoms in space

#6
Front (Question)

what are the 2 types of stereoisomers

Back (Answer)

• E/Z isomerism - optical isomerism

#7
Front (Question)

explain how E/Z isomers occur

Back (Answer)

• restricted rotation around the double bond • groups attached are fixed relative to each other • rigid due to high electron density

#8
Front (Question)

what are the conditions needed for E/Z isomerism

Back (Answer)

• C=C double bond - different groups attached to each carbon atom of the double bond

#9
Front (Question)

what is cis- trans isomerism

Back (Answer)

used to describe a special case of E/Z isomerism

#10
Front (Question)

what are the conditions needed for cis- trans isomers?

Back (Answer)

• C=C double bond • more than 2 different groups attached to each carbon atoms of the double bond • one of the attached groups on each carbon must be a hydrogen

#11
Front (Question)

what is a cis- isomer called in E/Z isomerism?

Back (Answer)

z

#12
Front (Question)

what is a trans- isomer called in E/Z isomerism?

Back (Answer)

E

#13
Front (Question)

how are groups prioritised in Cahn- Ingold- Prelog?

Back (Answer)

• priority bases on their atomic number - the group with higher atomic number at the 1st point of difference has higher priority

#14
Front (Question)

explain why alkenes are more reactive than alkanes

Back (Answer)

• pi bonds are more exposed than sigma electrons - pi bonds readily break and alkenes undergo addition reactions easily

#15
Front (Question)

electrophile definition

Back (Answer)

electron pair acceptor

#16
Front (Question)

what is the characteristic mechanism for alkenes

Back (Answer)

electrophilic addition

#17
Front (Question)

why is the tertiary carbocation more stable than the secondary and primary carbocation?

Back (Answer)

• each alkyl group donates and pushes electrons towards the positive charge of the carbocation • the more alkyl groups attached to the positively charged carbon atom, the more the change is spread out, making it more stable

#18
Front (Question)

how are carbocations classified

Back (Answer)

classified by the number of alkyl groups attached to the positively charged carbon atom

#19
Front (Question)

what do feedstock recycling describe?

Back (Answer)

describes the chemical and thermal processes that can reclaim monomers, gases, or oil from waste polymers

#20
Front (Question)

state 1 atmospheric pollutant caused by the burning of PVC

Back (Answer)

HCl(g)

#21
Front (Question)

how are polymers suitable for storing food and chemical safety?

Back (Answer)

lack of reactivity

#22
Front (Question)

what does recycling reduce?

Back (Answer)

reduces their environmental impact by conserving finite fossil fuels as decreasing the amount of waste going to landfill

#23
Front (Question)

what are the advantages of bio plastics?

Back (Answer)

• protect our environment - conserves valuable oil reserves

#24
Front (Question)

what is the advantage of feedstock recycling?

Back (Answer)

able to handle unsorted and unwashed polymers