alkanes (organic chem) Flashcards

hydrocarbons, fractional distillation of crude oil, uses of alkanes,cracking, combustion

1
Q

define โ€˜alkanesโ€™

A

saturated hydrocarbons

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2
Q

define โ€˜petroleum fractionโ€™

A

mixture of hydrocarbons with similar chain length & b.p range

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3
Q

gen. formula of alkanes

A

CnH(2n+2)

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4
Q

reactivity of alkanes

(and why?)

A

unreactive apart from combustion โ€“> strong, non-polar C-C & C-H bonds

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5
Q

process of fractional distillation of crude oil

A

> the petroleum fractions condense at diff. heights
the temp. of the column decreases upwards
smaller molecules condense at top โ€“> lower temp = lower b.p โ€“> smaller size โ€“> smaller VDWs
larger molecules condense at bottom โ€“> higher temp = higher b.p โ€“> larger size โ€“> larger VDws

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6
Q

smaller molecule characteristics

A
  • lighter colour
  • very flammable
  • low viscosity
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7
Q

larger molecule characteristics

A
  • darker colour
  • less flammable
  • high viscosity
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8
Q

vacuum distillation

A
  • heavy residue from fractionating column distilled under vac.
  • lowering the pressure over a liquid = lower b.p
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9
Q

why might vacuum distillation be used?

A
  • allows heavier fractions to be further seperated
  • no need for high temps โ€“> could break them down
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10
Q

define โ€˜crackingโ€™

A

conversion of long hydrocarbons to smaller, more useful hydrocarbon molecules by breakage of C-C bonds

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11
Q

high Mr alkanes โ€“>

A

smaller Mr alkanes + alkenes + (hydrogen)

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12
Q

name a solid material made from alkanes

A

polymer

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13
Q

why does cracking req. high temps?

A

involves splitting of strong cov. bonds (C-C)

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14
Q

list the economic reasons for cracking

A
  1. petroleum fractions with shorter C chains (eg. petrol) are higher in demand
  2. products of cracking = more valuable than starting materials
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15
Q

conditions for thermal cracking

A
  • high pressure (7000kPa)
  • high temp. (400-900 degrees)
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16
Q

products of thermal cracking

A
  • mostly alkenes
  • sometimes prod. hydrogen
17
Q

process of thermal cracking

A
  • proceeds via free radical mechanism
  • 1st step is homolytic fission of C-C bond
18
Q

conditions for catalytic cracking

A
  • slight pressure
  • high temp (450 degrees)
  • zeolite catalyst
19
Q

products of catalytic cracking

A
  • branched and cyclic alkanes
  • aromatic hydrocarbons
20
Q

why is catalytic cracking used?

A
  • branched/cyclic hydrocarbons burn more smoothly than unbranched ones โ€“> used to give fuels higher octane no.
  • cheaper than t. cracking โ€“> uses less energy โ€“> lower temp n pressure
21
Q

why are alkanes used as fuels?

A
  • they burn readily in presence of oxygen
  • this combustion of alkanes = highly exo.
  • can be used as fuels (fuels release heat energy when burnt)
22
Q

complete combustion

A
  • fuel + O2 โ€“> CO2 + H2O
  • excess O2
23
Q

incomplete combustion

A
  • fuel + O2 โ€“> C or CO + steam
    โ€“> CO = colourless, odourless, toxic gas which bonds to haemoglobin
    โ€“> C = causes global dimming, respiratory issues
  • insufficient O2
24
Q

types of pollution from combustion

A
  • sulphur impurities
  • nitrogen oxides
  • greenhouse gases
25
Q

sulphur impurities โ€“> SO2

(type of pollution)

A
  • found on coal
  • SO2 produced via incomplete combustion when sulfur is burnt
  • SO2 dissolves in water โ€“> acid rain
26
Q

removing SO2

A
  • removed from waste gases in furnace via flue gas desulphurisation
  • gases pass through scrubber with basic CaO โ€“> reacts with acidic SO2 in neutralisation reaction
27
Q

what is the product of flue gas desulphurisation?

(& itโ€™s use)

A

calcium sulphite โ€“> can be further made into calcium sulphate for plasterboard

28
Q

N + O2 โ€“> 2NO

A
  • high temp and spark in car engine provides sufficient emergy to break strong N2 bond
  • reacts with oxygen โ€“> prod. nitrogen oxides
  • dissolves in water โ€“> acid rain
29
Q

what do catalytic converters do?

A
  • remove carbon monoxide, nitrogen oxides & unburned hydrocarbons โ€“> convert them into harmless gases
  • has ceramic honeycomb coated with thin layer of catalyst metals โ€“> gives large S.A
30
Q

identify a catalyst in the converter

A

palladium, platinum

31
Q

why is UV light needed for the synthesis of chloroalkanes?

A

UV light supplies energy to break the Cl-Cl bond

32
Q

what is the process of breaking the bonds during initiation called?

A

homolytic fission

33
Q

free radical mechanism

(steps)

A
  1. initiation -> split halogen into free radicals
  2. propagation -> extract H from alkane
  3. propagation -> replace H in free radical alkane with halogen from diatomic molecule
  4. termination -> two radicals prod. stable molecule