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docboilproducts updated Feb 15th 2008 |
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Brown's Chemistry Clinic GCSE-KS4-IGCSE Science-CHEMISTRY Revision-information notes on OIL and its useful PRODUCTS and mention of other fossil fuels e.g. natural gas, coal and peat, and pollution-environment problems See also extra GCSE Organic Chemistry notes (may have what you want if not on this page and has a subsection-index and alphabetical keyword list) |
Oil Products multiple choice QUIZ: Foundation or Higher and 3 word-fill worksheets
The origin of oil
and other fossil fuels - what are they formed from?
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The
SEPARATION of the crude oil mixture into fractions and the USES of
these fractionsA fraction is a mixture of a restricted boiling point range of molecules, they have a similar number of carbon atoms and physical properties. The uses of the fractions depend on their physical and chemical properties. |
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| THE FRACTIONAL DISTILLATION OF CRUDE OIL | names of fractions | C atoms in the molecule | boiling range in oC | USES of the fraction - mainly depends on its physical properties - see below this table | |
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Fuel Gas, LPG, Refinery Gas | 1 to 4 | -160 to 20oC |
methane |
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| Gasoline, Petrol | 5 to 11 | 20 to 60oC | easily vaporised, highly flammable, easily ignited, car fuel | ||
| Naphtha | 7 to 13 | 60 to 180oC | no good as a fuel, but valuable source of organic molecules to make other things, cracked to make more petrol and alkenes | ||
| Paraffin, Kerosene | 10 to 16 | 120 to 240oC | less flammable than petrol, domestic heater fuel, jet fuel | ||
| Diesel oil, Gas oil | 15 to 25 | 220 to 250oC | car and larger vehicle fuel | ||
| Fuel and lubricating oils and Waxes | 20 to 70 | 250 to 350oC | not so easily evaporated, not as flammable, safe to store for central heating oil, quite viscous (sticky) and can also be used for lubricating oils, clear waxes and polishes | ||
| Bitumen | over 70 | over 350oC | forms a thick, black, tough and resistant adhesive on cooling, used as waterproofing material and to sticks rock chips on roofs or road surfaces | ||
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Down the list above the molecule gets ...
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The
ALKANE series of saturated
hydrocarbons Alkanes are a group of hydrocarbon molecules in which all the carbon and hydrogen atoms are only joined by single covalent bonds (e.g. C-H or C-C). Alkanes are known as saturated molecules because other atoms cannot add to them (compare alkenes further on). The first four in the series are shown. They are not very reactive unless burned! (1) is the molecular formula: a summary of the totals of each atoms of each element in one molecule; (2) is a 'shorthand' version of the full structural formula (3); (3) is called the structural formula: it shows how all the atoms are linked with the covalent bonds -; (4) is a '3D' representation of the structural formula (3). |
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(1) , (4)![]() |
methane (main molecule in natural gas) |
(1)
(4)![]() |
ethane |
(1)![]() |
propane |
(1)![]() |
butane |
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The reactions of Alkanes
Introduction
general word equation: hydrocarbon + oxygen ==> carbon dioxide + water word equations e.g. methane + oxygen ==> carbon dioxide + water and the corresponding symbol equation is CH4(g) + 2O2(g) ==> CO2(g) + 2H2O(l) Note that one CO2 for every C, and one H2O for every two H's in the hydrocarbon molecule.
In terms of displayed formula the equation would be written as ...
... in which every individual atom is shown and how it is bonded ('connected') with other atoms in the molecule. All the dashes represent the covalent bonds between the atoms in the molecules. Another example is the combustion of propane ... propane + oxygen ==> carbon dioxide + water C3H8(g) + 5O2(g) ==> 3CO2(g) + 4H2O(l) and in terms of displayed formula and balancing numbers ...
and the above diagrams show how the atoms have rearranged themselves in the reaction after the reactant bonds are broken (C-H, O=O and C-C in ethane etc. below)) and the new bonds formed in the products (C=O and O-H). Note the number of atoms of each element must be the same on each side of the equation (1C, 4H's and 4 O's, Law of Conservation of mass) and the products are different substances with different properties compared to the reactants. See Elements, Compounds and Mixtures page for more on writing and balancing equations. for ethane the more awkward symbol equation is ... 2C2H6(g) + 7O2(g) ==> 4CO2(g) + 6H2O(l) and for pentane the symbol equations is ... C5H12(l) + 8O2(g) ==> 5CO2(g) + 6H2O(l) The reaction of alkanes with chlorine is described on the Extra Organic Chemistry page |
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Atmospheric pollution
Part-1: The Incomplete
Combustion of hydrocarbons |
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Energy resource evaluation - What makes a good fossil fuel? Factors that should be taken into consideration
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The ALKENE
hydrocarbons series (unsaturated) Alkenes are hydrocarbons containing a carbon...carbon double bond (>C=C<) as well as single bonds. These are called unsaturated molecules because two atoms can join onto the bond when it opens up. The first two in the series are shown below. They are extremely reactive and important compounds in the chemical industry and are converted into very useful compounds e.g. plastics. They are made from cracking processes (see below) (1) is the molecular formula: a summary of the totals of each atoms of each element in one molecule; (2) is a 'shorthand' version of the structural or displayed formula (3); (3) is called the structural or displayed formula: it shows how all the atoms are linked with the covalent bonds - |
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(1) |
ethene |
(1) ,
(3)
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propene |
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(1) |
butene |
| Three important reactions of alkenes | |
| (1) Addition of bromine: A test to distinguish between ALKANE and ALKENE hydrocarbons | |
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ethene + bromine ==> 1,2-dibromethane |
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2nd example of bromine addition to a
double bond. propene + bromine ==> 1,2-dibromopropane |
| (2) Alkenes can add hydrogen to form a saturated alkane molecule | |
![]() propene + hydrogen ==> propane |
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| (3) Polymer formation - see PLASTICS section | |
![]() CRACKING
a problem of Supply and Demand!There isn't enough petrol in crude oil and crude oil doesn't have any alkenes in it for plastics but cracking reactions can help!
butane (2)
butane
(3)
C8H18
(4)
C12H26
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![]() The formation
of POLYMERS and the USES of PLASTICS - MacromoleculesReactions of alkenes (3) polymerisation/polymerization (a few more points on Extra Organic page) The formation of big polymer molecules called polyalkenes from small molecules called alkenes
Poly(ethene) from ethene is a cheap but very useful plastic used for plastic bags and bottles (old or commercial names: polyethylene, polythene and polyethene).
Poly(propene) from propene is stronger and more hard wearing than polythene and is used for making crates, fibres and ropes (old or commercial names: polypropylene, polyprene and polypropene).
Poly(chloroethene), PVC, made from chloroethene (old name vinyl chloride) is much tougher than poly(ethene) and very hard wearing with good heat stability. so it is used for covering electrical wiring and plugs. It is also replacing metals for use as gas and water drain pipes and has found a use as artificial leather and readily dyed to bright colours! (old names : polyvinyl chloride, shortened to PVC) Polystyrene* is made from styrene* (another alkene monomer) and is used in a gas expanded form for packaging and insulation. [*new names: poly(phenylethene) polymer made from phenylethene monomer] |
Atmospheric pollution Part-2:
Three
problems associated
with using and disposing of Polymers or Plastics
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Other very useful products from oil - despite the negative aspects! As well as plastics, there are lots of other useful compounds which can be made from the carbon based molecules of oil, e.g. look up drugs/esters on the extra GCSE organic chemistry page. Most are only dealt with at a more advanced level but the structural material, pharmaceutical and food industries have all developed a wide range of products in attempt to enhance our lifestyle and quality of life. |
![]() Atmospheric
pollution Part-3: Other
Pollution
aspects of the Petrochemical Industry
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docboilproducts updated Feb 15th 2008 |