4.1.3 alkenes Flashcards

1
Q

what is a sigma bond

A

when 2 s-orbitals directly overlap

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2
Q

what is a pi bond

A

sideways overlap of two p orbitals

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3
Q

draw diagram

A

in booklet

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4
Q

what is the bond angle in alkene

A

120 as there are 3 bonding regions of electrons which repel one another equally

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5
Q

what is a structural isomer

A

same molecular formula but different structural formula

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6
Q

what is stereoisomerism

A

same structural formula but different arrangements of atoms in space

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7
Q

what must a compound have for it to have E/Z isomerism
(type of stereoisomerism)

A

-a c=c double bond
-each carbon must have two different groups attached to it

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8
Q

e isomer

A

high priority groups are on the opposite side

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9
Q

z isomer

A

high priority groups are on the same side

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10
Q

cis/trans

A

each carbon has one of the same groups

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11
Q

cis

A

same group is on the same side

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12
Q

trans

A

same group is on the opposite sides

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13
Q

are alkenes or alkanes more reactive

A

alkenes as the pi bond has a lower bond enthalpy than the sigma bond

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14
Q

alkene to alkane

A

add H2
-nickel catalyst, 150 degrees

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15
Q

alkene to haloalkane

A

-add hydrogen halide
-NOTE- if alkene is unsymmetrical two products are possible

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16
Q

alkene to alcohol

A

-Add H2O (steam)
-phosphoric acid catalyst, 60 atm, 300 degrees

17
Q

testing for alkene

A

add bromine water
-decolourises from orange to colourless

18
Q

electrophile

A

electron pair acceptor

19
Q

heterolytic fission

A

breaking of a covalent bond so both electrons from the bond go to one atom

20
Q

curly arrows

A

show the movement of electron pairs

21
Q

what is the mechanism for an alkene called

A

electrophilic addition

22
Q

which carbocation is more stable and what does this mean about the amount of product formed

A

secondary carbocation intermediate is more stable than a primary carbocation intermediate
so more product is formed from a secondary carbocation intermediate

23
Q

how do simple monomer alkenes join together

A

simple monomer alkenes join together to form long chain polymers
the pi bond breaks to form new sigma bonds

24
Q

conditions for addition polymerisation

A

high pressure and a catalyst

25
draw the general equation for polymerisation
in booklet
26
how to name a polymer
poly(alkene)
27
What are three ways to dispose of plastics
Recycle them use them as organic feedstock Combust them to generate electricity
28
processing of waste polymers (energy production)
some polymers are difficult to recycle so they can be burnt to produce heat energy which can be harnessed to produce electricity
29
processing of waste polymers (removal of toxic waste product)
when plastics are burnt to make electricity they produce the toxic by-product HCL if waste products are processed to remove the PVC this problem can be avoided. Solvents have been developed to dissolve the PVC
30
how can polymers be processed in a sustainable way
use as organic feedstock
31
how do you remove HCL
react with an alkali/base eg-naOH
32
what is a biodegradable polymer
can be broken down naturally in the environment by microorganisms
33
what is a photodegradable polymer
can be broken down naturally over time by absorbing light
34