Crude Oil
ChemistryΒ· 4.7β4.18 (Section 4(b))Β· 18 min read
1. Composition of Crude Oilβ βββββ± 3 min
Crude oil is a non-renewable fossil fuel formed over millions of years from the remains of dead marine organisms, buried under sediment at high pressure and temperature.
Crude oil
A complex mixture of mostly alkane hydrocarbons, with chain lengths ranging from 1 carbon atom to over 70 carbon atoms.
A student claims crude oil is a pure compound. Explain why this statement is incorrect.
- 1
Pure compounds contain only one type of molecule, with a fixed boiling point.
- 2
Crude oil contains hundreds of different hydrocarbon molecules of varying chain lengths, each with a unique boiling point, so it is a mixture, not a pure substance.
Exam tip:
You will be asked to state that crude oil is a mixture of hydrocarbons in multiple exam questions, so memorise this core fact explicitly.
2. Fractional Distillation of Crude Oilβ β ββββ± 4 min
Fractional distillation separates crude oil into groups of hydrocarbons with similar boiling points, called fractions, in an industrial fractionating column. The column is hottest at the bottom (~350Β°C) and coolest at the top (~20Β°C).
Fraction
A group of hydrocarbons with similar chain lengths and boiling points, separated from crude oil for a specific commercial use.
Crude oil is heated to ~400Β°C to vaporise almost all of the mixture, then pumped into the bottom of the column. Shorter-chain hydrocarbons have lower boiling points, so they rise up the column and condense at cooler, higher levels. Longer-chain hydrocarbons have higher boiling points, so they condense at hotter, lower levels of the column, or remain liquid and are removed from the bottom.
Fraction (top to bottom) | Boiling point | Viscosity | Colour | Main use |
|---|---|---|---|---|
Refinery gases | Lowest (<40Β°C) | Runniest | Colourless | Bottled heating/cooking fuel |
Gasoline | 40β100Β°C | Very runny | Pale yellow | Petrol for cars |
Kerosene | 100β250Β°C | Runny | Yellow | Aircraft fuel, paraffin lamps |
Diesel | 250β350Β°C | Thick | Dark yellow | Lorry, car and generator fuel |
Fuel oil | 350β600Β°C | Very thick | Dark brown | Ship and power station fuel |
Bitumen | Highest (>600Β°C) | Most viscous | Black | Road surfacing, roof sealant |
State two properties of kerosene that differ from fuel oil, and explain the reason for the difference.
- 1
Kerosene has a much lower boiling point than fuel oil. This is because kerosene is made of shorter hydrocarbon chains that require less energy to turn to gas.
- 2
Kerosene is also far less viscous than fuel oil, as shorter hydrocarbon chains flow more easily than long, tangled chains.
Exam tip:
You will often be asked to order fractions by boiling point, viscosity or colour, so memorise the top-to-bottom sequence of fractions carefully.
3. Combustion of Hydrocarbon Fuelsβ β β βββ± 4 min
Fuel
A substance that releases heat energy when burned (combusted) with oxygen.
Hydrocarbons are used widely as fuels because they release large amounts of heat energy when burned. There are two types of combustion, depending on the amount of oxygen available.
Complete combustion occurs when there is a plentiful supply of oxygen. The only products are carbon dioxide and water vapour, and all energy stored in the hydrocarbon is released.
Incomplete combustion occurs when there is a limited supply of oxygen. Products are water vapour plus carbon monoxide (a toxic gas) and/or solid carbon (soot). Less energy is released than in complete combustion.
Carbon monoxide is a colourless, odourless toxic gas. It reduces the ability of blood to transport oxygen around the body, leading to unconsciousness or death if exposure is prolonged. You do not need to mention haemoglobin in your answers for this specification.
Write a balanced equation for the incomplete combustion of propane (CβHβ) to produce solid carbon and water vapour, including state symbols.
- 1
First write unbalanced reactants and products: CβHβ + Oβ β C + HβO
- 2
- 3
- 4
- 5
Add state symbols for final answer:
Exam tip:
Always check if a question specifies complete or incomplete combustion before writing an equation. If it says 'plenty of air', use complete combustion; if it says 'limited air', use incomplete.
4. Combustion Pollutants and Acid Rainβ β β βββ± 3 min
Burning hydrocarbon fuels releases several harmful atmospheric pollutants, in addition to carbon dioxide (a greenhouse gas).
Oxides of nitrogen (NOβ): In car engines, the very high temperature of combustion allows nitrogen and oxygen from the air to react together, forming nitrogen monoxide and nitrogen dioxide (collectively called NOβ).
Sulfur dioxide: Many hydrocarbon fuels contain small amounts of sulfur impurities. When the fuel is burned, these sulfur impurities react with oxygen to form sulfur dioxide gas.
Both NOβ and sulfur dioxide dissolve in rainwater in the atmosphere, reacting to form acidic solutions. This falls as acid rain, which damages stone buildings, kills aquatic life, and harms trees and plants.
Explain how burning petrol in a car engine leads to acid rain formation, even if the petrol has no sulfur impurities.
- 1
The high temperature inside the car engine causes nitrogen and oxygen from the air to react, forming oxides of nitrogen (NOβ).
- 2
NOβ gases rise into the atmosphere and dissolve in rainwater, forming acidic solutions that fall as acid rain.
Exam tip:
Do not confuse the source of NOβ: they come from air in the engine, not from the fuel itself. SOβ comes from sulfur impurities in the fuel.
5. Catalytic Cracking of Long-Chain Alkanesβ β β βββ± 4 min
Fractional distillation of crude oil produces more long-chain fractions (like fuel oil) than the global market demands, and not enough short-chain fractions (like gasoline for petrol). Cracking solves this supply-demand imbalance.
Cracking
A thermal decomposition reaction that breaks long-chain alkanes into shorter, more useful alkanes and alkenes.
Catalytic cracking uses a catalyst of silica or alumina, at a temperature of 600β700Β°C, to break the carbon-carbon bonds in long alkane chains. The products are always a mixture of at least one shorter alkane and at least one alkene.
The shorter alkanes are used to make higher-demand fuels like petrol, while the alkenes are used as feedstock to make polymers (plastics) and other organic chemicals.
Long-chain alkane CββHββ is cracked to produce propene (CβHβ) and one other alkane product. Write the balanced equation for this reaction.
- 1
The number of carbon and hydrogen atoms must be equal on both sides of the equation.
- 2
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Exam tip:
You must memorise the exact conditions for catalytic cracking: silica/alumina catalyst, 600β700Β°C. Marks are often lost for missing these details.
6. Common Pitfalls
Wrong move:
Stating that crude oil is a pure substance
Why:
Crude oil is a mixture of hundreds of different hydrocarbons, not a single compound
Correct move:
Always explicitly state that crude oil is a mixture of hydrocarbons
Wrong move:
Mixing up the order of fractions in the distillation column, e.g. putting bitumen at the top
Why:
Longer-chain hydrocarbons have higher boiling points, so they condense at the hotter bottom of the column
Correct move:
Recall the top-to-bottom order: refinery gases β gasoline β kerosene β diesel β fuel oil β bitumen
Wrong move:
Writing carbon dioxide as a product of incomplete combustion
Why:
Incomplete combustion has limited oxygen, so carbon is only partially oxidised to CO or C, not fully to COβ
Correct move:
Only include COβ as a product if the question specifies complete combustion
Wrong move:
Stating oxides of nitrogen come from sulfur impurities in fuel
Why:
NOβ form when nitrogen and oxygen from air react at high engine temperatures, not from fuel impurities
Correct move:
Separate sources: SOβ from sulfur impurities, NOβ from air in hot engines
Wrong move:
Forgetting cracking conditions or only writing alkenes as products
Why:
Exam questions award marks for recalling exact conditions and both alkane and alkene products
Correct move:
Always state silica/alumina catalyst, 600β700Β°C, and include one alkane + one alkene in cracking equations
7. Quick Reference Cheatsheet
Key Concept | Facts to Recall |
|---|---|
Crude oil | Mixture of hydrocarbons |
Fraction order (top to bottom) | Refinery gases β Gasoline β Kerosene β Diesel β Fuel oil β Bitumen |
Top column fraction trend | Lower boiling point, paler, less viscous |
Complete combustion products | COβ + HβO |
Incomplete combustion products | CO/C + HβO |
CO toxicity | Reduces blood oxygen transport capacity |
NOβ source | High temp reaction of Nβ and Oβ in car engines |
SOβ source | Combustion of sulfur impurities in fuels |
Acid rain cause | NOβ and SOβ dissolve in rainwater to form acids |
Cracking conditions | Silica/alumina catalyst, 600β700Β°C |
Cracking products | Shorter alkane + alkene |
Cracking purpose | Matches supply of long fractions to demand for short fractions |
8. Frequently Asked
What is the order of fractions from top to bottom of the fractional distillation column?
The order from top (lowest boiling point) to bottom (highest boiling point) is: refinery gases, gasoline, kerosene, diesel, fuel oil, bitumen.
Why is cracking of long-chain alkanes necessary?
Cracking solves the supply-demand imbalance: fractional distillation produces excess low-demand long-chain fractions (e.g. fuel oil) and insufficient high-demand short-chain fractions (e.g. gasoline for petrol).
What is the difference between complete and incomplete combustion products?
Complete combustion (plenty of oxygen) produces only carbon dioxide and water. Incomplete combustion (limited oxygen) produces water plus carbon monoxide and/or solid carbon (soot).
What's Next
Now that you have mastered crude oil content, you are ready to move on to the properties and reactions of alkanes, the main component of crude oil fractions. You will then learn about alkenes, the valuable product of cracking, including their characteristic reactions and use in polymer production. Make sure to practice past paper questions on fractional distillation and cracking, as these are high-frequency exam topics worth 3β6 marks per question. You should also practice balancing combustion and cracking equations to avoid losing easy marks in your exam.
