Alkanes Flashcards

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1
Q

What is crude oil?

A

⦾ Mixture of different HCs

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2
Q

How can you separate crude oil?

How can this be possible

A

⦾ Fractional Distillation

⦾ Different lengths of HCs have different bp.s

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3
Q

State the method for separating crude oil?

A

1 ⦾ Mixture vaporised + fed into fractionating column
2 ⦾ Vapors rise, cool + condense
3 ⦾ Products siphoned off for different uses

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4
Q

How are the short and long HC chains differentiated between?

A

⦾ Short C chains: lower bp.s - rise higher in column before reaching their bp - collected at top of column
⦾ Long C chains: higher bp.s - don’t rise v. high before reaching their bp. - condense - collect at bottom of column

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5
Q

What are the differences between short and long HC chains?

A

Short:
⦾ Low bp.
⦾ Reactive (easily ignited)
⦾ Runny

Long:
⦾ High bp.
⦾ ~Unreactive (not easily ignited)
⦾ Viscous

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6
Q

What is the general order in length for long HCs to short HCs?
What are their uses?

A
LONGEST to SHORTEST:
⦾ Gases - LPG, camping gas
⦾ Petrol (gasoline) - Petrol
⦾ Naphtha - processed to make petrochemicals
⦾ Kerosene (paraffin) - Jet fuel, Central Heating
⦾ Gas oil - Disel, Central Heating
⦾ Mineral oil - Lubricating oil
⦾ Fuel oil - Ships, Power stations
⦾ Wax, Grease - Candles, Lubrication
⦾ Bitumen - Roofing, Road surfacing
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7
Q

Why are long chain molecules cracked?

A

⦾ Not useful

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8
Q

What are the 2 main types of cracking?

A

1 ⦾ Thermal

2 ⦾ Catalytic

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9
Q

What is Thermal Cracking?

A

⦾ Produces alkanes + alkenes
⦾ High temps ~1200K
⦾ High Pa ~700kPa

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10
Q

What is Catalytic Cracking?

A

⦾ Produces aromatic compounds (with C rings)
⦾ Lower temps ~720K
⦾ Normal Pa
⦾ Zeolite catalyst

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11
Q

What is complete combustion?

Complete the equation for e.g. CH4?

A

⦾ React with sufficient Oxygen
⦾ Produce Carbon dioxide and Water
⦾ CH4 + 2O2 → CO2 + 2H2O

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12
Q

What is incomplete combustion?

Complete the equation for e.g. CH4?

A

⦾ React with insuffient Oxygen
⦾ Produce Carbon monoxide and Water (even C)
⦾ 2CH4 + 3O2 → 2CO + 4H2O

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13
Q

Why is Carbon monoxide dangerous?

A

⦾ Toxic gas
⦾ Odorless
⦾ Colourless

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14
Q

What can remove dangerous gaseous products?

A

⦾ Catalytic converters

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15
Q

How do catalytic converters work?

A

⦾ Uses rhodium catalyst

⦾ Convert harmful products into more stable products e.g. CO2 or H2O

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16
Q

What else can incomplete combustion produce?

And why is this dangerous?

A

⦾ Carbon particulates

⦾ Respiratory problems as they pollute air

17
Q

Why are Sulfur impurities dangerous in the atomosphere?

A

⦾ Lead to acidification of water in Earth’s atm

⦾ React to form Sulfuric acid - H2SO4

18
Q

How can Sulfur impurites be removed from waste products?

A

⦾ Flue gas desulfurisation
⦾ Use powdered CaCO3 or CaO and gypsum
⦾ Flue gases mix with alkaline slurry + acidic SO2 gas reacts with Ca compounds to form harmless salt
⦾ CaO(s) + SO2(g) → CaSO3(s)

19
Q

What are Nitrogen Oxides?

A

⦾ Series of toxic + poisonous molecules

⦾ NOx

20
Q

How is Nitrogen monoxide produced?

A

⦾ High Pa
⦾ High temp
⦾ In car engine
⦾ N2 and O2 in air react together

21
Q

What are the series of Nitrogen oxide reaction that can occur?

A

⦾ N2(g) + O2(g) → 2NO(g)

⦾ 2NO(g) + O2(g) → 2NO2(g)

22
Q

Draw out the reaction that occur when catalytic converters remove pollutants?
Start with: C3H8(g)

A

⦾ C3H8(g) + 5O2(g) → 3CO2(g) + 4H2O(g)
⦾ 2NO(g) → N2(g) + O2(g)
⦾ 2NO(g) + 2CO(g) → N2(g) + 2CO2(g)

23
Q

What is the Chlorination of Alkanes?

A

⦾ Alkanes react with Halogen in presence of UV light to produce halogenoalkanes

24
Q

What is a free radical?

A

⦾ Particle with an unpaired electron

25
Q

How do freed radicals form?

A

⦾ Covalent bond splits equally

⦾ Giving each species 1 electron

26
Q

Why are free radicals reactive?

A

⦾ Unpaired electron

27
Q

What is photochemical reaction?

A

⦾ Started by UV light

28
Q

What is a Free Radcial Substitution reaction?

A

⦾ H atom is substituted by Cl or Br

29
Q

What are the series of reactions that result for the synthesis of Chloroalkanes?

A

1 ⦾ Initiation
2 ⦾ Propagation
3 ⦾ Substitutions
4 ⦾ Terminations

30
Q

Explain Initiation?

A

⦾ Photodissociation
⦾ Sunlight provides (J) to split Cl-Cl bonds equally
⦾ Each gets 1 e-
⦾ Cl• - highly reactive free radical

                           Cl2 + (UV) → 2Cl•
31
Q

Explain Propagation?

A

⦾ Free radicals used up + made again
⦾ Cl• attacks methane
⦾ New methyl free radical attacks another Cl2
⦾ New Cl• can attack another CH4 until all Cl• or CH4 used up
Cl• + CH4 → •CH3 + HCl
•CH3 + Cl2 → CH3Cl + Cl•

32
Q

Explain Substitutions?

A
⦾ If Cl's in excess, H atoms on CH4 eventually replaced by Cl
⦾ You'l get: dichloromethane - CH2Cl2, 
trichloromethane - CHCl3
tetrachloromethane - CCl4
CH4 + Cl2 → CH3Cl + HCl
CH3Cl + Cl2 → CH2Cl2 + HCl
CH2Cl + Cl2 → CHCl3 + HCl
CHCl3 + Cl3 → CHCl4 + HCl
⦾ But if CH4 in excess, Cl will be used up quickly + products mostly chloromethane
33
Q

Explain Termination?

A

⦾ 2 radicals join to end chain reaction + form stable product:
•CH3 + Cl• → CH3Cl
•CH3 + •CH3 → C2H6
Cl• + Cl• → Cl2