Alkanes Flashcards

1
Q

Why are alkanes unreactive?

A

1. C-C bonds and C-H bonds are very strong so cannot break easily yo form stronger bonds with other elements that easily
2. Have no polar side groups

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2
Q

What are the two main reactions that take place with alkanes?

A

1. Combustion
2. Reaction with halogens in the presence of UV light

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3
Q

Why are alkanes used as fuels?

A

They readily burn in air and are highly exothermic

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4
Q

What are the products of complete combustion?

A

Carbon dioxide and water

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5
Q

What steps are in the mechanism for Free Radical Substitution?

A

Initiation
Propagation
Termination

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6
Q

Do free radicals have a charge?

A

No

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7
Q

What is a free radical?

A

A highly reactive species which has one or more unpaired electrons

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8
Q

What kind of bond among many will be broken?

A

The weakest one

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9
Q

How do we terminate the presence of free radicals?

A

Reacting free radicals with other free radicals

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10
Q

What is a petroleum fraction?

A

A mixture of hydrocarbons of similar length within the same range of boiling point

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11
Q

How then are heavy residues from the fractionating column separated?

A

Distillation under a vacuum

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12
Q

Define cracking

A

The conversion of large hydrocarbon molecules into smaller hydrocarbon molecules by the breakage of C-C bonds.

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13
Q

What is produced from the cracking of alkanes?

A

Small chain alkane + Alkene + Hydrogen

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14
Q

What are the economic reasons for cracking?

A

1. Smaller chain alkanes are much more valuable than large chain alkanes
2. Smaller chain alkanes have more uses and are in higher demand as a result

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15
Q

What are the two types of cracking?

A

1. Thermal
2. Catalytic

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16
Q

What are the requirements of thermal cracking?

A

High pressure of about 7000kPa
High temperatures of 400 to 900

17
Q

What are the requirements of catalytic cracking?

A

Low oressure
Low temperature of about 450
Zeolite catalyst

18
Q

What are the products of thermal cracking?

A

Small chain alkanes and sometime hydrogen

19
Q

What are the products of catalytic cracking?

A

Branched and cyclic alkanes
Aromatic hydrocarbons

20
Q

What is the advantage of catalytic cracking over thermal cracking?

A

Less energy costs due to the use of low pressure and temperature

21
Q

What is the molecular shape and bond angles of alkanes that have sp3 hybridisation?

A

Tetrahedral with a bond angle of 109.5 degrees

22
Q

What is the trend in boiling point of alkanes?

A

General increase as the carbon chains get longer

23
Q

Why is boiling point low with branched molecules?

A

Weaker intermolecular forces between chains so less energy is required to break them

24
Q

What is the solubility of alkanes

A

Insoluble in water but soluble in some organic solvents