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Chapter 14 - Alkenes

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Total cards: 21•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

general formula of an akene

Back (Answer)

CnH2n

#2
Front (Question)

general formula of a cyclic alkene

Back (Answer)

CnH2n-2

#3
Front (Question)

why are alkenes more reactive than alkanes

Back (Answer)

because they have a region of high electron density (the double bond) which allows them to undergo addition reactions by attracting electrophiles

#4
Front (Question)

whats an electrophile

Back (Answer)

electron pair acceptor

#5
Front (Question)

another name for double bond

Back (Answer)

pi bond

#6
Front (Question)

outline addition reactions with halogens (Br2)

Back (Answer)

Step 1 - The high electron density of the C=C double bond repels electrons in the bromine molecule, polarising the Br-Br bond. Step 2 - This leads to heterolytic fission of the Br-Br bond, with one bromine atom taking the bonding pair of electrons, creating a positively charged bromine which bonds to one of the carbon atoms. Step 3 - A positively charged carbocation intermediate forms. The negatively charged bromide ion then bonds to the other carbon atom. Step 4 - The final product, 1,2-dibromoethane, has a bromine atom bonded to each of the original alkene carbon atoms.

#7
Front (Question)

whats a carbocation

Back (Answer)

when a carbon atom is positively charged in a molecule

#8
Front (Question)

test for alkenes

Back (Answer)

decolorizes bromine water due to addition reaction with alkene

#9
Front (Question)

what conditions are used when hydrating alkenes to form alcohols

Back (Answer)

phosphoric acid 300 degrees Celsius 60 - 70 atm

#10
Front (Question)

what are primary secondary and tertiary carbocations

Back (Answer)

primary have one alkyl group attached, secondary have 2 and so on

#11
Front (Question)

why does the stability of carbocations increase with more alkyl groups

Back (Answer)

alkyl groups have a tendency to release electrons or a “positive inductive effect” which stabilizes the positive charge

#12
Front (Question)

what are major and minor products in electrophilic addtion

Back (Answer)

major product is made the most, it results from a more stable carbocation bonded to the electrophile

#13
Front (Question)

how can you get an alcohol from the products of an electrophilic addition reaction with sulfuric acid

Back (Answer)

Water and heat hydrolyse the alkyl hydrogen sulfate back to alcohols and sulfuric acid.

#14
Front (Question)

whats a polymer whats a monomer

Back (Answer)

monomer is one unit of a polymer polymer is long chain of monomers

#15
Front (Question)

why are alkenes used to make plymers

Back (Answer)

the C=C bond breaks to allow alkenes to join up and form a carbon chain

#16
Front (Question)

what process is joining together mnay monomers by breaking the C=C bond

Back (Answer)

addtion polymerisation

#17
Front (Question)

hwo does chain length affect physical properties of a plymer

Back (Answer)

Longer chains allow more surface contact between neighbouring chains. This strengthens the intermolecular forces.

#18
Front (Question)

hwo do branches affect physical properties of a plymer

Back (Answer)

Straight chains can pack together closely in an ordered structure, maximising intermolecular forces. Highly branched chains cannot pack as efficiently, reducing contact between chains.

#19
Front (Question)

what are plasticisers

Back (Answer)

plasticisers are small molecules that can be added to polymers to increase flexibility

#20
Front (Question)

how do plasticisers work

Back (Answer)

Plasticiser molecules position themselves between polymer chains. This pushes the chains apart, weakening intermolecular forces between polymer chains. The chains can now slide over each other more easily when bent.

#21
Front (Question)

why are addtion polymers unreactive

Back (Answer)

Polyalkenes contain only single covalent bonds. This makes them saturated compounds with maximum stability. They also have a carbon backbone lacking any polar groups, giving an overall non-polar molecule.