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What is crude oil, how is it separated into useful fractions, and why is it cracked?

Crude oil as a mixture of hydrocarbons, alkanes and their general formula, the fractional distillation of crude oil, the uses of the fractions, and the cracking of long-chain hydrocarbons.

A focused answer to OCR Gateway GCSE Chemistry A topic C6.2 on crude oil and hydrocarbons, covering crude oil as a mixture of hydrocarbons, alkanes and their general formula, the fractional distillation of crude oil and the uses of the fractions, and the cracking of long-chain hydrocarbons into alkanes and alkenes.

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  1. What this dot point is asking
  2. Crude oil and hydrocarbons
  3. Fractional distillation
  4. How the fractions change down the column
  5. Cracking

What this dot point is asking

OCR wants you to describe crude oil as a mixture of hydrocarbons, recognise alkanes and their general formula, explain how fractional distillation separates crude oil into fractions and their uses, and explain why and how cracking breaks long-chain hydrocarbons into smaller, more useful molecules including alkenes. This is the organic chemistry of fuels.

Crude oil and hydrocarbons

Fractional distillation

The main fractions, from the bottom (largest molecules) to the top (smallest), include bitumen (for road surfaces), fuel oil, diesel, kerosene (jet fuel), petrol, and refinery gases (for bottled gas). Most fractions are used as fuels.

How the fractions change down the column

Going down the column, the molecules in the fractions get larger (longer chains), and so they:

  • have higher boiling points,
  • are more viscous (thicker, flow less easily),
  • are less flammable (harder to ignite),
  • are less volatile (evaporate less easily).

The smaller molecules at the top are the most useful as fuels because they ignite easily and flow well.

Cracking

Notice that cracking conserves mass: the carbon and hydrogen atoms are rearranged, not created or destroyed, so the equation must balance.

Exam-style practice questions

Practice questions written in the style of OCR exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.

OCR 20186 marksCrude oil is separated into useful fractions by fractional distillation. Describe how fractional distillation separates crude oil into fractions, and explain how the properties of the fractions change from the top to the bottom of the column.
Show worked answer β†’

A six-mark Level of Response question. Reward describing the process: the crude oil is heated until it evaporates (vapourises) and the vapour enters the bottom of the fractionating column, which is hot at the bottom and cooler at the top (a temperature gradient). As the vapours rise, they cool, and each fraction condenses (turns to liquid) when it reaches a part of the column at its boiling point: fractions with high boiling points condense low down (where it is hot) and fractions with low boiling points rise higher before condensing (near the cooler top). The fractions are collected at different heights. Then explain the trend: going down the column, the hydrocarbon molecules in the fractions get larger (longer chains), so they have higher boiling points, are more viscous (thicker), are less flammable (less easily ignited) and are less volatile. Markers reward the heating and vapourising, the temperature gradient, fractions condensing at their boiling points at different heights, and the trends in molecule size, boiling point, viscosity and flammability. A common error is to say the oil is separated by melting point.

OCR 20214 marksA long-chain hydrocarbon from crude oil is cracked. Explain what is meant by cracking, why long-chain hydrocarbons are cracked, and name the two types of product formed.
Show worked answer β†’

A C6.2 structured question. Reward: cracking is the breaking down (thermal decomposition) of long-chain hydrocarbon molecules into smaller, more useful molecules, using a high temperature and a catalyst (or steam). Long-chain hydrocarbons are cracked because there is a greater demand for shorter-chain hydrocarbons (such as petrol) than is produced by fractional distillation alone, so the less useful long chains are broken into more useful short ones; cracking also produces alkenes, which are used to make polymers (plastics) and other chemicals. The two types of product are shorter-chain alkanes and alkenes. For example C10H22β†’C8H18+C2H4\text{C}_{10}\text{H}_{22} \rightarrow \text{C}_8\text{H}_{18} + \text{C}_2\text{H}_4. Markers credit cracking as breaking long molecules into smaller ones using heat (and a catalyst), the reason (demand for short chains and for alkenes to make polymers), and the products (a shorter alkane and an alkene). A common error is to say cracking joins molecules together.

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