Fossil fuels
Fuels are substances that react with oxygen to release energy in exothermic combustion reactions.
Coal forms from remains of plants and crude oil forms from animals and bacteria in oceans and lakes. They were not able to rot without regular oxygen. Intense pressure and heat resulted in their formation over millions of years. All release energy upon burning.
Coal, natural gas and petroleum are fossil fuels that produce carbon dioxide in combustion.
Natural gas is mainly made of methane.
Petroleum is a mixture of hydrocarbons. It is separated into useful fractions by fractional distillation.
Combustion
Complete Combustion: CnHn + O2 → CO2 (g) + H2O (g) using a hydrocarbon fuel
Incomplete Combustion: CnHn + O2 → CO (g) + H2O (g) carbon monoxide is poisonous!
Incomplete combustion happens when there is a lack of oxygen.
Fractional distillation
Separates liquids using different boiling points, and hydrocarbons have a range of boiling points due to impurity. Small, volatile, low-boiling point molecules that flow easily and ignites easily has less intermolecular attractive forces and hence takes less energy to seperate, they will be at the top of the fractional distillation columns. Big molecules with higher boiling points has more intermolecular attractive forces and takes more energy to separate, and they settle at the bottom of fractional distillation columns.
Distillation of crude oil (petroleum)
Name | Boiling point | # of carbons | Uses |
Refinery gases | 20° | 1-4 | Bottled gas for heating and cooking |
Petrol/Gasoline | 70˚ | 5-10 | Car fuel |
Naphtha | 120˚ | 8-12 | Chemical uses |
Kerosene | 170˚ | 10-16 | Jet fuel |
Diesel oil | 270˚ | 16-20 | Big car fuel/ diesel engines |
Fuel oil | 260-340˚ | 30-40 | fuel |
Bitumen | 340˚ | 50+ | Road building |
Alkanes
They are homologous family of hydrocarbons with similar properties.
They are saturated combustible fuel that has single bonds. Generally unreactive except when burning.
Generic formula: CnH2n+2
Methane, ethane, propane, butane, pentane, hexane, etc.
Alkenes
They are unsaturated hydrocarbons with one double bond between 2 carbon atoms. They are more reactive as double bond is less stable.
CnH2n
Ethene, propene, butene, pentene, hexene, etc.
Cracking
Cracking produces alkenes. It’s a chemical reaction that breaks down long hydrocarbons into smaller ones, produce is random.
Large moleculed alkane /longer alkane → shorter alkane + alkene
Conditions: aluminum/silicon (3) oxide catalyst (porcelain catalyst), high temperature and pressure
Bromination of ethene / test for unsaturation
C2H4 + Br2 → C2H4Br2
Bromine is brown-yellow solution that when shaken with ethene will turn colorless very fast at room temperature.
Product is bromoethane. If the solution remains colored, then hydrocarbon is an alkane.
This is an addition reaction.
Hydrogenation of ethene / addition reaction
C2H4 + N2 → C2H6
Hydrogen is added across the double bonds to make it a saturated alkane, increasing the melting point. A nickel catalyst is used. 150°C Temperature.
Hydration of ethene / addition reaction
C2H4 + H2O → C2H6O
Adding water turns ethene into ethanol/alcohol. This is purer than fermentation, and product is used in medicine and science. Phosphoric acid is a catalyst, and under heat and pressure.
Alcohol
Complete combustion: C2H6O + 3O2 → 2CO2 + 3H2O
Ethanol is widely used as a solvent in many perfumes and cosmetics and as a fuel.
Polymerizations
Macromolecules are large molecules built up from smaller units (monomers) and they have different units for different macromolecules.
There are two ways to make a polymer:
Addition: monomers bond and rearrange, no atoms are lost.
2000 atm, 200˚C and O2 impurity.
Ethene | Polythene | ||
Propene | Polypropylene | ||
Vinyl chloride | Polyvinyl chloride |
These are used in making plastics.
Condensation polymerization: Molecules (usually water) are lost as byproducts.
Nylon is made from reacting diamine with dicarboxylic acid. Water is produced. This is called a polyamide as it is joined up by amide links as pictured.
Reversible under alkaline or acidic conditions.
Natural macromolecules
Protein has the same amide linkages like nylon but they are formed with amino acids.
Proteins can be hydrolysed to amino acids under acid or alkaline conditions.