Alkanes and Petroleum Processing

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Question-and-answer flashcards covering properties of alkanes, fractional distillation, fuel improvement processes, combustion, and environmental considerations.

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21 Terms

1
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What are alkanes?

Saturated hydrocarbons containing only single covalent bonds; general formula CₙH₂ₙ₊₂.

2
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What type of bonding is present in alkanes?

Strong sigma (σ) bonds between C–C and C–H atoms formed by overlap of s and/or p orbitals.

3
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Why are alkanes relatively unreactive?

They possess strong C–C and C–H bonds and are non-polar molecules.

4
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Which reactions do alkanes commonly undergo?

Combustion and free-radical substitution.

5
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How are alkanes found in nature?

Primarily in crude oil (petroleum), formed from fossilised organisms over millions of years.

6
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What is petroleum?

A complex mixture of alkanes (and some other hydrocarbons) of varying chain lengths that must be separated and processed.

7
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How is crude oil separated into useful fractions?

By fractional distillation in a fractionating column based on differing boiling points.

8
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Describe the main steps of fractional distillation of crude oil.

Crude oil is vaporised (~350 °C), vapour enters a hot-bottom/cool-top column, hydrocarbons condense at heights corresponding to their boiling points.

9
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How does chain length affect condensation height in fractional distillation?

Shorter-chain hydrocarbons condense higher up; longer-chain hydrocarbons condense lower down.

10
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List the main fractions obtained from crude oil from top to bottom.

Gases, petrol (gasoline), naphtha, kerosene, diesel, lubricating oils & waxes, fuel oil, bitumen.

11
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What problems do straight-chain alkanes have as fuels?

Lower octane numbers, less power output, and can cause engine knocking.

12
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Name the three key industrial processes used to improve fuel quality.

Cracking, reforming, and isomerisation.

13
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What is cracking?

The breaking of long-chain alkanes into shorter, more useful hydrocarbons such as petrol and alkenes.

14
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Differentiate thermal cracking and catalytic cracking.

Thermal: high T & P; Catalytic: moderate T (~450 °C), low P, zeolite catalyst.

15
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Why is catalytic cracking important?

Produces branched alkanes, aromatics, and alkenes used for high-octane fuels and polymer feedstocks under milder conditions.

16
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What is reforming?

Conversion of straight-chain alkanes into branched or aromatic hydrocarbons to raise octane number using a platinum catalyst.

17
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What is isomerisation?

Rearrangement of straight-chain alkanes into branched-chain isomers with higher octane ratings.

18
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What are the products of complete combustion of alkanes?

Carbon dioxide (CO₂) and water (H₂O).

19
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What are the products of incomplete combustion of alkanes?

Carbon monoxide (CO) or carbon (soot) plus water (H₂O).

20
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List five environmental issues associated with alkane combustion.

CO₂ (global warming), CO (toxic), NOₓ (acid rain, respiratory issues), unburned hydrocarbons (smog), soot (respiratory problems, global dimming).

21
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What do catalytic converters do and how?

Using a platinum/rhodium catalyst, they convert CO, NOₓ, and unburned hydrocarbons in exhaust gases into less harmful CO₂, N₂, and H₂O.