Alkanes from Crude Oil Flashcards

1
Q

where does most of the energy we use globally come from

A

burning fossil fuels

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2
Q

what are the typical fossil fuels

A
  • coal
  • natural gas
  • oil
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3
Q

what are most crude oils and natural gases

A

alkanes

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4
Q

what are the three main processes used to convert crude oil into fuels

A
  • fractional distillation
  • cracking
  • reforming
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5
Q

what is crude oil

A

a complex mixture of compounds, mainly hydrocarbons

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6
Q

why is fractional distillation sometimes called fractionation

A

because it involves converting the crude oil into a small number of fractions

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7
Q

where is fractional distillation done

A

in a distillation column

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8
Q

what is firstly done to the crude oil before it enters the distillation column

A
  • it is heated in a furnace
  • for most of it to be turned into vapour
  • which is then passed into the column near the bottom
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9
Q

what is special about the fractionating column which allows the different hydrocarbons to separate

A
  • it has a temperature gradient

- it is hot at the bottom and gets cooler as you go up

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10
Q

what happens when the vapor passes up the column through a series of bubble caps

A
  • different fractions condense at different heights of the column
  • depending on the boiling temperature range of molecules in that fraction
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11
Q

what kind of molecules would you see near the bottom of the column

A
  • the molecules would be larger
  • have longer chains
  • and therefore have higher boiling points
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12
Q

what kind of molecules would you see near the top of the column

A
  • the molecules would be smaller
  • which shorter chains
  • and therefore have lower boiling points
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13
Q

does all of the vapor condense and why

A
  • all of it doesnt condense
  • as some of the hydrocarbons are dissolved gases
  • so it reaches the very top
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14
Q

why is the demand for shorter hydrocarbons larger than longer hydrocarbons

A
  • the world has fewer uses for longer hydrocarbons

- and shorter ones make for good fuel and are able to be used when making polymers and other substances

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15
Q

due to there being a surplus of longer hydrocarbons and deficit of shorter ones, what has been the solution to balancing out the demand to supply ratio

A
  • converting the longer chains into shorter ones

- which is what cracking is

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16
Q

how is cracking done

A
  • you pass the heavier hydrocarbons through a heated catalyst
  • this causes the larger molecules to break up into smaller ones
  • so from one large molecule, at least two smaller ones are formed
17
Q

what is a common catalyst used for cracking

A
  • zeolite

- which is a compound of aluminium, silicon and oxygen

18
Q

what could decane, C10H22, be cracked into and what are they used for

A
  • octane C8H18 used for petrol

- and ethene C2H4 used for making polymers

19
Q

what is an advantageous point about cracking, specifically about the different types of hydrocarbons used and produced

A
  • only alkanes are used for cracking as they require the least energy
  • but from it you can get alkanes and alkenes
20
Q

what is a disadvantage or uncertainty that comes with using alkanes as fuels in cars (other than pollution…)

A
  • during the combustion that takes place in car engines

- not all hydrocarbons of the right size burn the same way

21
Q

what kind of hydrocarbons burn more and less efficiently

A
  • straight chain hydrocarbons burn less efficiently

- those with branched chains and rings (cyclic compounds) burn more efficiently

22
Q

what does the process of reforming do

A
  • it converts straight chain alkanes into branched chains and cyclic hydrocarbons
  • by heating them with a catalyst
23
Q

what would the catalyst be for reforming

A

platinum

24
Q

what is the advantage that comes with reforming

A

it allows the fuel to burn more smoothly (efficiently) with oxygen in the engine

25
Q

what would pentane turn into if it was reformed

A
  • it has the formula C5H12
  • it would be turned into cyclopentane with a formula of C5H10
  • meaning the byproduct s hydrogen, H2
26
Q

what would heptane, 7H16 convert into if it was reformed

A
  • methylbenzene
  • with hydrogen as the byproduct, 4H2
  • it is a cyclic hydrocarbon with a circle in the middle but not an alkene
27
Q

what is another positive that comes with reforming of this nature

A
  • the byproduct is hydrogen

- which is as very useful product