alkenes Flashcards

1
Q

describe the trend in boiling point in alkenes

A

as carbon chain gets longer
there are more london forces
: mp/bp gets higher

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2
Q

are alkenes unsaturated/saturated and why

A

unsaturated hydrocarbon
contains at least one c=c double bond

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3
Q

what is the general formula of alkenes

A

CnH2n

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4
Q

what is the exception for the general formula of alkenes

A

cyclic alkenes have 2 less hydrogens
CnH2n-2

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5
Q

where do reactions occur in alkenes and why

A

they occur at the pi bond because pi bond is weak (electronegativity is spread over a wider distance)

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6
Q

how to name an alkene

A

no. of Cs - no. C = is on - ene

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7
Q

how to name an alkene with another element on it

A

no. its on - x no. of Cs - no. = is on - ene

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8
Q

how do you draw alkenes

A

on a horizontal slant

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9
Q

when do E Z isomers occur

A

if the groups bonded to each carbon atom in the C=C bond are different

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10
Q

what do E isomers look like

A

sideways z

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11
Q

what do z isomers look like

A

a bathtub

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12
Q

describe an E isomer

A

trans isomer
groups not same on either side at double bond

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13
Q

describe Z isomer

A

cis isomer
groups same on either side at double bond

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14
Q

what are the rules of EZ isomers

A

both sides of double bond have to contain 2 different side chains

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15
Q

what is ule 3 of EZ isomers

A

looing t position of top/bottom of priority across double bond
if they are same side (e.g. both top then Z)

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15
Q

what is rule 2 of EZ isomerism

A

we assign priority groups on each side at double bond by atomic number

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16
Q

define free radicals

A

A species with an unpaired electron

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17
Q

define electrophile

A

species that accepts a pair of electrons from a nucleophile to form a bond

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18
Q

define nucleophile

A

species that donate a pair of electrons
shown at Nu:

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19
Q

define an addition reaction

A

2 reactants added together to form one product

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20
Q

define substitution reaction

A

2 reactants to -> 2 products
Swapped over atoms from one reactant to another

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21
Q

define an elimination reaction

A

Start with 1 reactant and take something out of it, forming 2 products
Often taking away water

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22
Q

define redox reaction

A

Involves colour changes often - from reactant inorganic substance that is reduced
Tend to see it with alcohol going to carboxylic acids

23
Q

define organic oxidation

A

gain of oxygen/loss of hydrogen

24
define organic reduction
loss of oxygen/gain of hydrogen
25
define homolytic fission
breaking covalent bond between halogen producing free radical
26
define heterolytic fission
pair of electrons from the covalent bod moves individual element gains electron from covalent bond and one element loses electron in covalent bond (the element is a halogen)
27
what do curly arrows show
movement of pairs of electrons can be pair on element, can move into covalent bond
28
what is Markovnikov's rule
Alkene addition mechanism: Intermediate that has our positive carbon (carbocation) determines the stable carbocation
29
according to Markovnikov's rule,
Stability occurs when the carbocation has the most number of "C's" around it
30
what kind of product is the more stable carbocation product
major product
31
what kind of product is the less stable carbocation product
minor product
32
how do you turn an alcohol into a haloalkane
with sodium halide and H2SO4
33
how to turn a haloalkane into alcohol
add NaOH and reflux
34
how to turn alcohol into an alkene
with concentrated H2SO4
35
how to turn an alkene into alcohol
hydration of alkene add H2O (g) and H3PO4 catalyst
36
how to turn an alkene into a haloalkane
add hydrogen halide
37
how to turn an alkene into an alkane
hydrogenate the alkene with H2 and a Ni catalyst at 432K
38
how to turn an alkane into a haloalkane
using a halogen or UV
39
what could happen with hydration of alkenes when attempting to form alcohols
multiple products with asymmetrical alkenes
40
what are the two different types of polymerisation
addition - alkanes condensation
41
what is the general reaction for polymers forming from alkenes
alkene double bond broken by high temp and pressure and forms a polymer
42
what are the pros of using polymers to store food and chemicals
they are very unreactive
43
what are the pros of recycling polymers -2
reduces environmental impact by conserving finite fossil fuels decreasing the amount of waste going to landfill
43
what are the problems with disposing of polymers
lots are non-biodegradable they build up in the environment, damaging it - killing marine wildlife
44
describe the stages of polymers being recycled
sort polymers into types chopped into flakes washed, dried and melted cut into pellets and used my manufacturers
45
what is the issue with PVC recycling
it is hazardous due to high chlorine content and additives dumping PVC in landfill isn't sustainable
46
how are waste polymers used as fuels
polymers that are derived from petroleum or natural gas have a high energy stored value making them difficult to recycle Waste polymers can be incinerated to produce heat, generating steam to drive a turbine to produce energy
46
what happens when PVC is burnt
it releases hydrogen chloride a corrosive gas and other toxins like dioxins
47
what is feedstock recycling
The chemical and thermal processes that reclaim monomers, gases or oil from waste polymers
47
how has new technology changed how PVC is dealt with
previously: grinding PVC and using it to manufacture new products now: dissolves polymer using solvents - then recovered by precipitation from the solvent, then solvent is used again
48
what are the products of feedstock recycling
they resemble those produced from crude oil refineries These materials can be used as raw materials for the production of new polymers
49
what is an advantage of feedstock recycling
it is able to handle unsorted and unwashed polymers
50
what are the pros of biodegradable polymers 2
protects our environment conserves valuable oil reserves
51
what are biodegradable molecules
Bioplastics produced from plant starch, cellulose, plants oils, and proteins offer a renewable and sustainable alternative to oil-based products
52
what are photodegradable polymers
polymers contain bonds that are weakened by absorbing light to start the degradation. Alternatively, light-absorbing additives are used