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
Q

draw the general equation for polymerisation

A

in booklet

26
Q

how to name a polymer

A

poly(alkene)

27
Q

What are three ways to dispose of plastics

A

Recycle them use them
as organic feedstock
Combust them to generate electricity

28
Q

processing of waste polymers
(energy production)

A

some polymers are difficult to recycle so they can be burnt to produce heat energy which can be harnessed to produce electricity

29
Q

processing of waste polymers
(removal of toxic waste product)

A

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
Q

how can polymers be processed in a sustainable way

A

use as organic feedstock

31
Q

how do you remove HCL

A

react with an alkali/base eg-naOH

32
Q

what is a biodegradable polymer

A

can be broken down naturally in the environment by microorganisms

33
Q

what is a photodegradable polymer

A

can be broken down naturally over time by absorbing light

34
Q
A