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Ch.13 Alkenes

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

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#1
Front (Question)

When naming do you prioritise the double bond or an alkyl or halogen substituent

Back (Answer)

Double bond

#2
Front (Question)

What is a pi bond

Back (Answer)

Covalent bond formed from the sideways overlap of 2 adjacent P orbitals creating an area of electron density above and below the plane of the molecule, each carbon contributes 1 electron

#3
Front (Question)

What is a stereoisomer

Back (Answer)

Same molecular formula and same structural formula, yet different arrangement of the atoms in space

#4
Front (Question)

What is needed for an E/Z isomer

Back (Answer)

. C=C bond . Each C must be bonded to 2 different groups

#5
Front (Question)

What is needed for a cis-trans isomer

Back (Answer)

. C=C . Both C must be bonded to 2 different groups, but one group must be common to both carbons

#6
Front (Question)

what is a Cis isomer

Back (Answer)

Common group on same side of C=C

#7
Front (Question)

what is a Trans isomer

Back (Answer)

Common group on opposite side of C=C

#8
Front (Question)

In E/Z isomers each C attached group is given priority based on their what

Back (Answer)

Atomic number

#9
Front (Question)

An E isomer is when

Back (Answer)

2 highest priority groups are on opposite sides of the C=C (Entgegan)

#10
Front (Question)

A Z isomer is when

Back (Answer)

The 2 highest priority groups are on the same side of the C=C

#11
Front (Question)

When assigning priority you look for the

Back (Answer)

First point of difference

#12
Front (Question)

Why are alkenes reactive

Back (Answer)

Relatively low bond enthalpy of the pi bond. the pi electrons are more exposed as they are above and below the plane.

#13
Front (Question)

How could you test for unsaturation

Back (Answer)

Alkenes react with bromine water- colour change from orange to colourless Alkanes don’t react with bromine water so there won’t be a colour change

#14
Front (Question)

Markownikoffs rule

Back (Answer)

The H will attach its self to the C of the C=C with the most hydrogens

#15
Front (Question)

What degree of carbocation is the most stable and why

Back (Answer)

Tertiary because alkyl groups are electron donating. Each alkyl group push electrons towards the cation. the + charge is spread out making it more stable.

#16
Front (Question)

The major product is

Back (Answer)

The product with the most stable carbo cation intermediate

#17
Front (Question)

Alkenes undergo polymerisation at

Back (Answer)

High temp and pressure using a catalyst

#18
Front (Question)

what is the bond shape around the c in a c=c bond

Back (Answer)

trigonal planar 120*

#19
Front (Question)

what does unsaturated mean

Back (Answer)

at least 1 c=c

#20
Front (Question)

explain the cahn-ingold-prelog rule for naming E-Z isomers

Back (Answer)

each atom attached to the c of a c=c bond is given priority based on its atomic number. if the 2 highest priority are on the same side it is a Z isomer and the oposite would be an E isomer.

#21
Front (Question)

how do you assign priority when naming E/Z isomers

Back (Answer)

start with the atoms directly bonded if same atomic number move on until you find the first point of difference.

#22
Front (Question)

what is the difference between the primary and secondary carbocation

Back (Answer)

primary- has + charge on end of chai. secondary- has + charge in middle of chain.

#23
Front (Question)

how can u recycle PVC

Back (Answer)

dissolve in a solvent then recover by precipitation, solvent can be used again.

#24
Front (Question)

what is feedstock recycling and give an advantage

Back (Answer)

chemical/thermal process of regaining monomers from waist polymers. it produces raw materials for the production of new polymers. can be done with unsorted unwashed polymers.