2.5 Crude Oil, Fuels and Organic Chemistry Flashcards

(80 cards)

1
Q

What are hydrocarbons

A

Compounds containing ONLY carbon and hydrogen atoms

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2
Q

What is a hydrocarbon chain

A

Carbon atoms forming bonds with other carbon atoms

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3
Q

Longer the hydrocarbon chain- higher or lower the boiling point

A

Higher

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4
Q

What is crude oil

A

A complex mixture of hydrocarbons formed over millions of years from the remains of simple marine organisms

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5
Q

How can crude oil be separated

A

Fractional distillation

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6
Q

Temperature of the fractionating column

A

It has a temperature gradient- high at bottom low at top

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7
Q

What happens to crude oil before it enters the fractionating column

A

It is boiled/vaporised

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8
Q

The lower the boiling point the——in the column the compound is collected

A

Higher

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9
Q

What are fractions

A

Mixtures containing hydrocarbon compounds with similar chain lengths therefore similar boiling points

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10
Q

Why do larger hydrocarbon chains have higher boiling points

A

Molecules are held together by intermolecular forces- larger molecules, more intermolecular forces; more energy needed to overcome them in order to melt/boil

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11
Q

Longer chain molecules are more or less viscous

A

More viscous- harder to pour

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12
Q

Where in the fractionating column are small molecules found

A

Top

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13
Q

Where in the fractionating column are large molecules found

A

Bottom- high b p

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14
Q

What does burning hydrocarbons require and produce

A

Requires O2 from the air
Produces carbon dioxide and water

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15
Q

Equation for burning methane in air

A

CH4➕2O2➡️CO2➕2H20

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16
Q

Why are the shorter chain hydrocarbons better fuels

A

Easier to vaporise

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17
Q

Economic and political issues of the oil industry

A

Price of oil =set by oil producing countries(poor countries who need oil have to pay going rate- not in control of their economy)
War affects oil supply, this could affect economy
Political disagreement countries can cut off others oil supply

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18
Q

Social and environmental issues of the oil industry

A

Burning fossil fuels- increase global warming
Oil spills- cause major pollution incidents
Power Plant- eye sore /spoils countryside and habitats

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19
Q

Ethanol isn’t a hydrocarbon but
What does burning ethanol in air produce

A

Same products as burning hydrocarbons
CO2 and water

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20
Q

Burning ethanol- what happens if supply of oxygen is limited

A

Incomplete combustion
Forming carbon (soot) and carbon monoxide (poisonous) in addition to usual products(water and co2)

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21
Q

What does the combustion of fuel containing impurities (e.g compounds of sulfur) form

A

Sulfur dioxide causing acid rain

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22
Q

What does burning hydrogen produce
Equation

A

Only water
2H2➕O2➡️2H2O

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23
Q

advantages of hydrogen as a fuel

A

Renewable
No CO2 emissions when burned

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24
Q

Disadvantages of using hydrogen as a fuel

A

Made by reacting steam with coal/gas or passing electricity through water (electrolysis)- not carbon neutral - CO2 produced
Very flammable- dangerous

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25
Catalytic cracking definition
Large hydrocarbons can be broken into smaller ones
26
How does catalytic cracking work What is also formed
Heating heavier fractions to a high temp in the presence of a catalyst An alkene is also formed
27
Why is catalytic cracking done
There is a greater demand for smaller hydrocarbons Alkenes are used to make plastics
28
Properties of plastics
Good thermal and electrical insulator Flexible strong low density don’t rot/corrode
29
Formula for the chemical symbol of an ALKANE
CnH2n+2
30
Formula for the chemical symbol of an ALKENE
CnH2n
31
Alkane structure
n carbons bonded together by single bonds, H atoms wherever else possible single bonds
32
What are alkenes
Unsaturated hydrocarbons which have a double bond between 2 carbon atoms
33
Each C atom has— bonds around it (structure)
4
34
What are isomers
Molecules which have the same molecular formula but different structures and physical properties
35
Isomerism in alkenes
The C=C double bond is in a different position- noted by the number
36
What does saturated mean (alkenes/alkanes)
They have the maximum possible amount of hydrogen Contain only single bonds(so more bonds are available)
37
Addition reactions
2 atoms can be added **across the C=C bond in an unsaturated compound**, forming a**saturated compound** One atom is added to each of the carbon atoms
38
What is turned when hydrogen is added to an alkene (hydrogenation)
The corresponding alkane is formed
39
Testing for alkenes
Bromine water Goes from orange/brown to colourless
40
Br-Br ➕ H H C=C H H
H Br H-C-C-H Br H
41
Br2➕C2H4 Product name
BrCH2CH2Br Dibromoethane
42
Alkane molecules can be assembled together in large numbers to make
Polymers
43
What are thermoplastics
Soften when heated
44
What are thermosets
Resistant to heat (don’t soften when heated)
45
Thermoplastics made up of
Polymer chains that aren’t linked; can slide over each other
46
Thermosets made up of
Strong cross linkages holding polymer chains together
47
What are small molecules used to form polymers called
Monomers
48
What are addition polymers made up of
One type of monomer
49
What are condensation polymers made up of
2+ types of monomer
50
What happens to the bonds in Polymerisation
One of the bonds from the double bond breaks to allow the molecules to join another
51
Polypropene uses
Dishwasher safe food containers Piping Car parts Prop**ene**= pip**ing**, eng**ine** (car parts)
52
Polytetrafluoroethene (PTFE) uses
Teflon- non stick coating
53
Poly(vinyl chloride) (PVC) uses
Pipes Door frames Insulation
54
Issues with plastics (disposal)
Non biodegradable Increases pressure on landfill for waste disposal
55
Advantages of recycling
Less plastic goes to landfill- sites can be used for longer Less oil needed for plastic production- crude oil = a finite resource; must be conserved wherever possible Less energy consumed
56
Naming alkanes/enes Saturated- no C=C bonds- ends in ?
Ane
57
Naming alkanes/enes Contains a C=C bond- ends in?
Ene
58
How to name the substituent groups
Ending -yl Name according to number of carbon atoms the group has 1=methyl 2=ethyl 3= propyl
59
What is a substituent group
groups of atoms which are attached to the central carbon chain
60
Add a prefix to the substituent group name to show…
How many substituent groups there are in total 2- do 3- tri etc
61
Alcohols formula for chemical formula
CnH2n+1OH
62
Where is the OH group of the alcohol name ends in 1-ol
First C atom
63
Where is the OH group if the alcohol name ends in 2-ol
On second C
64
Which alcohol is used in alcoholic drinks
Ethanol
65
Process of fermentation
Yeast produces ethanol from sugar in anaerobic conditions
66
How is the fermentation reaction catalysed
By enzymes produced by yeast
67
Fermentation conditions
Must be kept sterile O2 must be kept out CO2 must escape or pressure will build up
68
Glucose➡️carbon dioxide➕ethanol
C6H12O6➡️2CO2➕2C2H5OH
69
Testing for alcohols
Alcohols reacts with a solution of potassium dichromate(VI) Mixed with sulphuric acid, it turns from orange to green
70
What is ethanol as a fuel?
A biofuel produced using plant material
71
Advantages of ethanol as a fuel
Renewable as produced from plant material Emits less CO2 than petrol on burning plants take up CO2 When grown - carbon neutral Burning ethanol produces s less soot and carbon monoxide
72
Disadvantages for ethanol as a fuel
Fossil fuels are used in its production It’s a less efficient fuel more is needed Engines must be modified Large amounts of farmland used, not available for food+ deforestation
73
What can ethanol be made into - acid found in vinegar What type of acid is this What type of reaction is this Carries out in what conditions
Ethanoic acid Carboxylic acid Oxidation aerobic conditions
74
Test for an alkene
Add orange bromine water It will go colourless
75
Step 1 naming complex alkanes/alkenes
Length of parent/longest chain Are there double bonds? Yes = alkene No = alkane
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Step 3 naming complex alkanes/alkenes Example
Number and type (how many carbon atoms in a) substituent group e.g. tri (3 group) methyl (they each have one carbon) hexane (longest chain is 6 carbons long)
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Step 4 of naming complex alkanes/alkenes
Position of the substituent groups 2, 2, 4 if 2 are joined to second carbon and one is joined to 4th carbon 2,2,4 tri methyl hexane
78
Step 2 naming complex alkanes/alkenes
Numbering carbon atoms First carbon is on end nearest to a substituent group
79
What does the n in ((e.g.hex))-n-ene represent
Placement of the double bond (lowest number it’s attached to)
80
What do carboxylic acids (e.g. ethanoic acid) contain
A carboxylic group -COOH