alkanes (organic chem) Flashcards

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

1
Q

define β€˜alkanes’

A

saturated hydrocarbons

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2
Q

define β€˜petroleum fraction’

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 –> 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 –> lower temp = lower b.p –> smaller size –> smaller VDWs
larger molecules condense at bottom –> higher temp = higher b.p –> larger size –> 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 –> could break them down
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10
Q

define β€˜cracking’

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 –>

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 –> used to give fuels higher octane no.
  • cheaper than t. cracking –> uses less energy –> 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 –> CO2 + H2O
  • excess O2
23
Q

incomplete combustion

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

types of pollution from combustion

A
  • sulphur impurities
  • nitrogen oxides
  • greenhouse gases
25
sulphur impurities --> SO2 | (type of pollution)
* found on coal * SO2 produced via **incomplete combustion** when sulfur is burnt * SO2 dissolves in water --> **acid rain**
26
removing SO2
* removed from waste gases in furnace via **flue gas desulphurisation** * gases pass through scrubber with basic CaO --> reacts with acidic SO2 in neutralisation reaction
27
what is the product of flue gas desulphurisation? | (& it's use)
calcium sulphite --> can be further made into c**alcium sulphate** for plasterboard
28
N + O2 --> 2NO
* **high temp** and spark in car engine provides **sufficient** emergy to **break** strong N2 bond * reacts with oxygen --> prod. nitrogen oxides * dissolves in water --> **acid rain**
29
what do catalytic converters do?
* remove carbon monoxide, nitrogen oxides & unburned hydrocarbons --> convert them into **harmless** gases * has ceramic honeycomb coated with **thin** layer of **catalyst metals** --> gives **large** S.A
30
identify a catalyst in the converter
palladium, platinum
31
why is UV light needed for the synthesis of chloroalkanes?
UV light supplies **energy** to **break** the Cl-Cl bond
32
what is the process of breaking the bonds during initiation called?
homolytic fission
33
free radical mechanism | (steps)
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