alkenes Flashcards

1
Q

what is an alkene

A

unsaturated hydrocarbons with a C=C double bond

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2
Q

what is the general formula of an alkene

A

CnH2n

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3
Q

why no rotation about the C=C double bond

A

due to pi orbital - electron density above and below the single bond, which holds the carbon atoms in place

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4
Q

are alkenes more or less reactive than alkanes

A

more reactive, due to high electron density of double bond and the fact the pi-bond is slightly easier to break

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5
Q

what intermolecular forces of attraction do alkenes have

A

only van der waals due to non-polar bonds

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6
Q

are alkenes soluble in water

A

no

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7
Q

3 kinds of isomerism alkenes can have

A

chain isomers
position isomers
geometric E-Z isomers

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8
Q

what is an electrophile

A

electron deficient atoms/ions which accept a pair of electrons

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9
Q

what is the most stable kind of carbocation intermediate

A

alkyl groups have a positive inductive effect, so the most stable carbocation is the one bonded to the most other carbon atoms

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10
Q

major products will be formed from which kinds of carbocations

A

tertiary

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11
Q

what conditions are needed for the electrophilic addition of H2O to an alkene

A

acid catalyst, usually phosphoric acid

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12
Q

what are the products of the reaction

A

an alcohol

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13
Q

what conditions are needed for the electrophilic addition of a hydrogen halide to an alkene

A

room temperature

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14
Q

what conditions are needed for the electrophilic addition of a halogen molecule to an alkene

A

room temp and an organic solvent

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15
Q

how does a molecule with a non-polar bond react as if it is an electrophile

A

C=C double bond with a high electron density induces a temporary dipole in the halogen molecule –> delta positive atom attracted to double bond

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16
Q

how would you turn the product into an alcohol and how does show that sulfuric acid catalyses the addition of water to an alkene

A

add water

H2SO4 reforms, showing it catalyses the hydration of alkenes

17
Q

what is an addition polymer

A

many monomers bonded together via rearrangement of bonds without the loss of any atom or molecules

18
Q

what are monomers and what form do they usually take

A

molecules which combine to form a polymer

usually have a C=C bond which breaks to leave a repeating pattern

19
Q

give 3 uses of poly(cholorethene)

(PVC)

A

drainpipes
vinyl
aprons

20
Q

give two examples of plasticisers

A

esters
phthalates

21
Q

what are plasticisers

A

small molecules that get between polymer chains to force them apart and allow them to slide over one another

22
Q

how do the physical properties of PVC change due to a plasticiser

A

PVC with plasticiser become flexible, used for aprons

without, it is rigid and used for drainpipes

23
Q

why do things containing mainly C-C and C-H bonds not decompose easily

A

bonds are non-polar so are not attacked by enzymes

24
Q

why is a lack of biodegrabability in compounds with C-C or C-H bonds a problem

A

disposal is problematic

25
Q

what is mechanical recycling

A

where plastics are separated into different types, washed, ground down, melted and re-moulded

26
Q

what is mechanical recycling used for

A

soft drinks bottles –> fleeces

27
Q

what is feedstock recycling

A

plastics heated to a temperature which break polymer bonds, leaving original monomers that can be made into new plastics

28
Q

what is feedstock recycling used for

A

making totally new plastics

29
Q

what is a problem with recycling

A

each time thermosoftening plastics are melted and remoulded, their properties degrade, so they can only be remoulded a limited number of times