Alkanes

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32 Terms

1
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What is petroleum?

A mixture of hydrocarbons that is predominantly alkenes.

2
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How can petroleum be separated?

By fractional distillation.

3
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What are the three types of alkane?

Unbranched alkanes

Branched alkanes

Cyclic alkanes

4
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Why do straight chain alkanes have a higher boiling point than branched alkanes?

They have more surface area in contact with each other, so the van der waals forces are stronger.

5
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What is cracking?

Splitting larger hydrocarbons up into smaller hydrocarbons.

6
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What is an alkane?

A hydrocarbon that only contains single bonds.

7
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What is the general formula for an alkane?

CnH2n+2

8
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What are the two types of cracking?

Thermal cracking

Catalytic cracking

9
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What are the conditions for thermal cracking?

High temperature and high pressure

10
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What hydrocarbons are produced from thermal cracking?

Mostly alkenes.

11
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What are the conditions for catalytic cracking?

High temperature, slight pressure and with the aid of a zeolite catalyst.

12
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What hydrocarbons are produced by catalytic cracking?

Motor fuels and aromatic hydrocarbons.

13
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What are the economic benefits of cracking?

It produces more valuable products like motor fuels and alkanes.

14
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State a common use of alkanes.

Fuels

15
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What products are produced in complete combustion?

Water and carbon dioxide

16
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What products are produced in incomplete combustion?

Carbon monoxide and/or carbon and water

17
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What types of pollution are produced by internal combustion engines?

Nitrogen oxides, carbon dioxide, carbon monoxide, carbon and unburnt hydrocarbons.

18
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19
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How can pollutants from internal combustion engines be controlled?

Catalytic converters in vehicles.

20
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What is the essential condition for free radical substitution?

UV light

21
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What is the organic reactant in free radical substitution?

The alkane

22
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What is a free radical?

A substance with one unpaired electron

23
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Are free radicals reactive or unreactive?

Very reactive.

24
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What is the overall reaction in free radical substitution?

Alkane + Halogen —→ Halogenoalkane + Hydrogen-halogen molecule

25
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What are the three stages in free radical substitution?

  1. Initiation

  2. Propagation

  3. Termination

26
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Why must UV light be present for the reaction to start?

It provides enough energy to homolytically break the covalent bonds in the halogens.

27
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What does homolytically mean?

The bond breaks symmetrically.

28
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What happens when the halogens split?

One atom each from the covalent bond goes to each atom, producing 2 free radical halogens.

29
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What role does the halogen play in the mechanism?

It is a catalyst.

30
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What are the two stages of propagation?

  1. One free radical reacts with a molecule of the alkane to form the by-product and an alkane free radical

  2. The alkane free radical reacts with another halogen to produce a halogenoalkane and another halogen free radical.

31
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What happens in the termination step?

2 free radicals react to form a neutral molecule

32
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What are the three possible reactions in termination?

Halogen + halogen

Halogen + alkane

Alkane + alkane