12.3- INDUSTRIAL CRACKING Flashcards

1
Q

Is the naphtha fraction from the fractional distillation of crude oil in huge demand?

A

yes

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2
Q

Why is the naphtha fraction in huge demand?

A

for petrol and by the chemical industry

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3
Q

What are longer chain fractions described as, as they’re not as useful?

A

they’re of lower value economically

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4
Q

What happens to meet the demand for shorter chain hydrocarbons?

A

many of the longer chain fractions are broken into shorter lengths (cracked)

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5
Q

What are the useful results of cracking? (2)

A

shorter, more useful chains produced, especially petrol

some of the products are alkenes, which are more reactive than alkanes

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6
Q

What is petrol a mixture of?

A

mixture of mainly alkanes containing between 4-12 carbon atoms

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7
Q

What are alkenes used as?

A

as chemical feedstock and are converted into a huge range of other compounds including polymers + variety of products from paint to drugs

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8
Q

What is probably the most important alkene?

A

ethene

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9
Q

Why is ethene perhaps the most important alkene?

A

starting material for poly(ethene) and wide range of other everyday materials

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10
Q

Why are harsh conditions needed to break down alkanes?

A

because they’re very unreactive

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11
Q

Two different types of cracking?

A

thermal cracking

catalytic cracking

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12
Q

What does thermal cracking involve?

A

heating alkanes to a high temperature, under high pressure

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13
Q

What high temperature is used for thermal cracking?

A

700-1200 K

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14
Q

What high pressure is used for thermal cracking?

A

up to 7000 kPa

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15
Q

What happens to carbon-carbon bond in thermal cracking?

A

carbon-carbon bond breaks in such way that one electron from the pair in the covalent bond goes to each carbon atom

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16
Q

So initially what is produced when the carbon-carbon bond is broken? (cracking)

A

initially two shorter chains are produced, each ending in a carbon atoms with an unpaired electron

17
Q

What are the fragments ending in a carbon atom with unpaired electrons called?

A

free radicals

18
Q

How reactive are free radicals and in what way do they react?

A

highly reactive intermediates + react in number of ways to form a variety of shorter chain molecules

19
Q

What is produced in thermal cracking?

A

alkane and alkene

20
Q

Why is an alkene produced in thermal cracking?

A

there’s not enough hydrogen atoms to produce 2 alkanes

21
Q

How many carbon-carbon bonds may break and does it have to be in the middle in thermal cracking?

A

any number of carbon-carbon atoms may break

chain does not necessarily have to break in the middle

22
Q

What may be also produced in thermal cracking?

A

hydrogen

23
Q

What does thermal cracking tend to produce a high proportion of?

A

high proportion of alkenes

24
Q

What is done to avoid too much decomposition (ultimately to carbon and hydrogen) after thermal decomposition?

A

alkanes are kept in thermal cracking conditions for a very short time, typically one second

25
Q

At what conditions is catalytic cracking carried out? (3)

A

lower temperature- about 720K

lower pressure- but more than atmospheric

zeolite catalyst- consisting of silicon dioxide and aluminium oxide

26
Q

What is the structure of zeolite like?

A

honeycomb structure with enormous surface area

27
Q

Is zeolite acidic or alkaline?

A

acidic

28
Q

What is catalytic cracking mainly used for?

A

mainly to produce motor fuels

29
Q

What are the products of catalytic cracking mostly like? (3)

A

mostly branched alkanes, cycloalkanes (rings), and aromatic compounds

30
Q

How are the products obtained from catalytic cracking separated?

A

by fractional distillation

31
Q

In a lab what can be the catalyst for catalytic cracking?

A

lumps of aluminium oxide

32
Q

What are the products mostly in catalytic cracking in a lab?

A

mostly gases- shows they have chain lengths of less than C5

33
Q

What does the mixture from catalytic cracking in a lab do to bromine solution?

A

decolourises bromine solution

34
Q

What is the bromine solution a test for?

A

test for carbon-carbon double bond showing the products contain alkenes