Alkenes Flashcards

(31 cards)

1
Q

What is the alkene structure

A

It is a planar molecule with 120 degree angles

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2
Q

What are the bonds in an alkene

A

Sigma bond between carbon and hydrogen
One sigma bond between the two carbons
One Pi bond between the two carbons

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3
Q

How is a pi bond formed

A

In the alkene there are two free electrons on each carbon, they have a P-orbital that overlaps and creates a pi bond

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4
Q

Why are alkenes highly reactive

A

Pi bonds have a lower bond enthalpy than sigma bonds because the sideways orbital is more unstable that the direct orbital

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5
Q

Why are hydrogen halide molecules attracted to the double bond

A

They have a permanent dipole and the double bond is an area of high electron density

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6
Q

What is created in the intermediate stage of electrophilic addition

A

A carbocation and a halogen ion

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7
Q

What is a primary carbocation

A

A carbocation where the positive charge is on the first carbon (only bonded to one alkyl group)

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8
Q

What is the minor product

A

The least common product of unsymmetrical electrophilic addition

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9
Q

Why are secondary carbocations more common

A

The positive carbon is bonded to and stabilised by two alkyl groups so it can survive by itself for longer so is more likely to form a product

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10
Q

How is an induced dipole created in a halogen molecule

A

The high electron density of the double bond repels the electrons in the halogen molecule bond

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11
Q

How do you test for an alkene

A

With bromine water, it will go colourless- creating a haloalkene

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12
Q

What is the structure of sulfuric acid

A

H2SO4
A double bonded oxygen above and below the carbon
An OH on either side of the carbon

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13
Q

Why does H act as an electrophile

A

The oxygen it is bonded to is very electronegative so the oxygen has slight negative charges and the hydrogen slight positive

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14
Q

What is the first product of an alkene and sulfuric acid

A

A carbocation intermediate and a hydrogensulfate ion with a negative oxygen

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15
Q

What is the product of a carbocation and a hydrogensulfate ion

A

Ethylhydrogensulfate (depends on number of carbons for first group)

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16
Q

What does Ethylhydrogensulfate and water produce

A

Ethanol and sulfuric acid

17
Q

What is the overall reaction of an alkene and sulfuric acid

A

Alkene + water –> Alcohol (with sulfuric acid as a catalyst)

18
Q

How do you get ethanol for Ethylhydrogensulfate

A

Water takes the place of the hydrogen sulfate

19
Q

What carbon is hydrogen more likely to bond to in the first stage

A

The first carbon/ the carbon bonded to the greatest number of hydrogen atoms

20
Q

What is a polymer

A

A large molecule made from thousands of small identical molecules called monomers

21
Q

What are the monomers of addition polymers

22
Q

What are the conditions of polymerisation

A

High temperature
High pressure
A catalyst

23
Q

What happens when an alkene forms a polymer

A

The double bond opens up and joins one monomer to another

24
Q

What is the name of polymerised ethene

25
Why are addition polymers unreactive
They contain lots of carbon-hydrogen and carbon-carbon bonds which are non-polar and relatively strong, so difficult to break
26
How do you draw a repeating unit
Take two adjacent carbon atoms Draw them with anything above or below Draw square brackets around them draw a covalent bond from each carbon atom extending through the bracket The number to the right shows how many units are in the chain
27
What is a plasticiser
A small molecule that fits between the polymer chains which causes the chains to move further apart which weakens the intermolecular forces between the chains
28
What is the effect of a plasticiser
The polymer chains can move over each other which makes the polymer more flexible
29
What is the advantage of addition polymers lack of reactivity
They can be used for food and substance containers without reacting with the things inside
30
What is the disadvantage of addition polymers
They don't biodegrade Microorganisms don't break them down and so they pollute the environment and damage organisms They also require crude oil to make which is a non-renewable resource, and also needs energy to be transported and refined Also occupy a lot of space in landfill
31
How can we reduce the environmental impact of addition polymers
They can be combusted which generates energy (but can release harmful chemicals) Can be sorted into different polymers and is recycled into new products Feedstock recycling - waste polymers are converted back to simpler hydrocarbons and then made into new polymers