2. alkanes Flashcards

1
Q

crude oil [4]

A

non renewable resource

formed when animal remains are buried under high temperature and pressure in the absence of O2 over millions of years

it is a valuable resource used in the process of making fuels, plastics, medicines

alkanes are the main constituent of crude oil

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

alkanes are saturated hydrocarbons. what does this mean?

A

saturated - each C forms max bonds. there are only C-C

hydrocarbons - consist only of H and C

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

process of fractional distillation []

A
  1. Oil is heated to evaporation in blast furnace. it enters fractionating column
  2. has a temp gradient where it is hottest at the bottom
  3. short chain molecules have lower BP bc weaker imf and condense nearer the top
  4. separate into fractions [fractions are mixtures of hydrocarbons with sim chain lengths and uses] of similar boiling points and chain lengths
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is fractional distillation based on

A

a physical process based on different bps and molecule sizes. it splits the weak vdw forced between molecules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

def of cracking

2 types

A

breakdown/ conversion of long chain HCs into SC HCs by breaking C-C bonds

this is done bc shorter chain alkanes are more in demand and more useful

there is catalytic and thermal cracking

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

conditions and products of catalytic cracking

A

zeolite catalyst
high temp of ~450C
moderate pressure

produces branched alkanes, cyclic alkanes, aromatic hydrocarbons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

conditions + products of thermal cracking

A

high temperature 800
high pressure 7000kPa

produces alkenes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

fuel

why are alkanes good fuels

A

smth that releases heat energy when burned/ combusted

they burn readily in oxygen, highly exothermic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

why is incomplete combustion not good

what can it form []

A

releases less energy/mole and forms pollutants

NOx gases
SO2
C
CO
unburnt HCs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what makes something a GHG

A

polar bonds

absorbs ir radiation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what do catalytic converters do and what catalysts do they use

A

they are in cars to remove CO and NOx and unburnt HCs to give CO2, N2 and H2O.

2CO+ 2NO - 2CO2 + N2

unburnt HC chains react with NO to form CO2, N2 and water

it will have a platinum, palladium or rhodium catalyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

flue gas desulfurization

A

SO2 can be removed from flue gases using calcium oxide or calcium carbonate

CaCO3 + SO2 -> CaSO3 + CO

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

why are alkanes unreactive

why do they react with halogens in UV light and what do they form

A

little polarity

UV light has more energy providing Ea for bonds to break. in presence of UV X-X bond in halogen molecules break to form halogen free radicals

f radicals are atoms/molecules with an unpaired electron

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

general process of alkane + free radical

A

alkane + free radical -> alkane radical + hydrogen halide

alkane radical + halogen molecule -> h.alkane + halogen radical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

steps to free radical substitution

A

INITIATION
UV forms f radicals from halogen molecules

PROPAGATION
molecule + radical -> molecule + radical

TERMINATION
- desired product
- halogen molecule
- side reaction where two alkane radicals form. in Qs always do structural formula

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

how has frs depleted the ozone layer

A

the synthesis of chlorofluorocarbons to be used as coolants or refrigerants was bad because they are unreactive so rise to stratosphere where UV is stronger. the CCl bond breaks and forms Cl• which reacts with O3 as a catalyst. one Cl• cand destroy thousands O3s.