13.1 -13.5 Flashcards

1
Q

What are alkenes

A
  • unsaturated hydrocarbon
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2
Q

What are unsaturated compounds

A
  • compounds that have at least 1 double covalent bonds
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3
Q

What is the general formula for alkenes

A
  • CnH2n
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4
Q

What type of reactions do alkenes undergo

A
  • Electrophilic addition reactions
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5
Q

What makes alkenes fairly reactive

A
  • the fact that they have a high electron density due to the double bond
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6
Q

What are the two bonds that alkenes have

A

1) sigma bonds
2) pi bonds

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7
Q

What type of bonds do all covalent molecule have

A
  • sigma bonds
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8
Q

Complete the sentence:
Sigma bonds have a high…

A
  • bond enthalpy
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9
Q

What are sigmas bonds

A
  • a horizontal overlap of 2s orbitals
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10
Q

What are pi bonds

A
  • the parallel overlap of 2p orbitals
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11
Q

Why are pi bonds weaker than sigma bonds

A
  • as the electron density in pi bonds is spread out above and below the nuclei so there is a weaker pi bond
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12
Q

Why do pi bonds have a lower bond enthalpy

A
  • because the electrostatic attraction is weaker
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13
Q

Are alkanes or alkenes more reactive and why

A
  • alkenes because they have 4 electrons being shared in the double bond and as the pi bond has a low bond enthalpy
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14
Q

Why are alkenes open to attack from electrophiles

A
  • as it has a high electron density
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15
Q

Define the term stereoisomers

A
  • when they have the same structural formula but a different arrangement of atoms in space
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16
Q

What is the shape and bond angle of the C=CH2

A
  • Trigonal planer (120)
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17
Q

Fill in the blanks:
Atoms can’t _______ around the C=C double bond and it is ____

A

1) rotate
2) rigid

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18
Q

When do we get E/Z isomerism

A
  • where you have 2 different atoms or groups of atoms on the same carbon
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19
Q

What do you do when deciding if an isomer is E or Z when we have 4 different groups around the double bond

A
  • use CIP rules
    1) number carbons 1 & 2
    2) find which atom has priority on each side by working out the atomic number
    3) they look at where the two high priorities are and distinguish whether it is E or Z isomerism
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20
Q

What are electrophiles

A
  • an electron pair acceptor which forms covalent bonds
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21
Q

What is the charge of electrophiles

A
  • positive
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22
Q

What are examples of electrophiles

A
  • NO2 +
  • H+
  • H-Br
  • H2SO4
23
Q

Where does the curly arrow start and go towards in electrophilic addition reactions

A
  • from the double bond to the electrophile
24
Q

How do alkenes become alkanes

A
  • reagent: H2
  • catalyst: Ni
25
Q

How do we test for alkenes

A
  • the discolouration of bromine water
    (browny-orange to colourless)
26
Q

What is the electrophiles in the test from alkenes

27
Q

What is formed when testing for alkenes

A
  • dibromoalkane
28
Q

How do alkenes from alcohols

A
  • hydration of alkenes
    Reagent: steam
    Catalyst: phosphoric acid (H3PO4)
29
Q

How do alkenes form halogenoalkanes

A
  • alkene + hydrogen haldies
  • in an electrophilic reaction
30
Q

What does the stability of carbocation intermediate determine

A
  • the amount of the 2 products
31
Q

What determines the stability of the intermediate and why

A
  • the amount of alkyl groups bonded to it
  • because the alkyl push electrons towards the positive carbocation stabilising it.
32
Q

Complete the sentence:
The more stable the carbocation the…

A
  • more likely it will form
33
Q

Complete the sentence:
Minor products are…

A
  • less stable and formed less often
34
Q

Complete the sentence:
Major products are…

A
  • more stable and formed more often
35
Q

What is Markownikoff’s rule

A
  • that the major product will be formed when the hydrogen adds to the carbon with the most number of hydrogens already attached
36
Q

What can we use alkenes to make

A
  • polymers
  • petrochemicals
37
Q

Fill in the blank:
Alkenes are _____ which join to form addition polymers

38
Q

What are the two types of polymers

A

1) Natural- proteins
2) Synthetic- poly(ethene) etc

39
Q

Why do we dispose of plastics

A
  • as they are polymers and most of them are not biodegradable and so need to be disposed carefully
40
Q

What are the 3 ways we dispose of non-biodegradable plastics

A

1) landfill
2) recycling
3) incineration(burning)

41
Q

What type of plastics are landfill useful for disposing

A
  • plastics too difficult to recycle
  • plastics too difficult to separate from other materials
  • not enough plastics to extract to make it economically viable
42
Q

What is the problem with disposing plastics in landfill

A
  • isn’t sustainable as large amounts of land is needed
  • becoming increasingly expensive to use land for waste
43
Q

Why do we recycle plastics

A
  • as plastics are made from crude oil which is non-renewable so recycling means we are reducing our dependency on crude oil for making plastics
44
Q

What are the two things we can do with recycled plastics

A

1) some plastics can be RE-MOULDED into new objects
2) other plastics are cracked into monomers to be used to make new plastics

45
Q

When do we use incineration

A
  • when the plastic can’t be recycled
46
Q

What do we use the energy from burning plastics to do

A
  • to generate electricity
47
Q

What is the problem with burning plastics

A
  • they can release toxic fumes
  • especially PVC which produces HCl
48
Q

How do we overcome the problem of toxic gases being released in incineration

A
  • use fuel gas scrubbers
  • which neutralise the acidic gases by firing bases
49
Q

How do biodegradable polymers decompose

A
  • naturally under certain conditions by organisms
50
Q

How are biodegradable polymers made

A
  • from oil fractions and renewable sources
51
Q

What is the problem with biodegradable polymers compared to non-biodegradable polymers

A
  • they are more expensive
52
Q

What are the certain conditions that biodegradable plastics need to decompose

A
  • good oxygen supply
  • moisture
53
Q

What are biodegradable plastics used for

A
  • protective sheets for plants