Alkanes Flashcards

1
Q

What is an alkane?

A

A saturated hydrocarbon containing only C-H bonds

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2
Q

What is the general formula of an alkane?

A

CnH2n+2

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3
Q

Explain why their bonds are non-polar

A

Carbon and hydrogen have similar electronegativities
Non-polar bonds means Van der Waals forces

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4
Q

What is the solubility and reactivity of alkanes?

A

Insoluble in water
Very reactive

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5
Q

How does fractional distillation work?

A
  1. Crude oil heated
  2. Passed into column that’s cooler at the top
  3. Vapours rise up the column and condense at their boiling points
  4. Shorter hydrocarbons condense closer to the top
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6
Q

What are the pro and cons of cracking?

A

+ reduces imported gas and electricity
+ gas supply for many years
- lots of traffic to local areas
- pollutes water supplies

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7
Q

Why are alkanes cracked?

A

To turn longer chain alkanes in shorter ones
More economically valuable

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8
Q

What are the conditions for thermal cracking?

A

Temperature = 1200K
Pressure = up to 700kPa

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9
Q

What are the conditions for catalytic cracking?

A

Temperature = 720K
Lower pressure
Zeolite catalyst

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10
Q

What are the main products of catalytic cracking?

A

Cycloalkanes
Aromatic hydrocarbons
Branched alkanes

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11
Q

What is a fuel?

A

Something which releases heat energy when combusted

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12
Q

What is incomplete combustion?

A

Combustion in a limited supply of oxygen
Produces carbon monoxide (toxic)
Typically longer chain hydrocarbons

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13
Q

What are the environmental impacts of some of these compounds?

A

Nitrogen oxides —> acid rain
Sulfur dioxide —> acid rain
Carbon / Soot —> global dimming
Unburnt hydrocarbons —> photochemical smog
Carbon dioxide —> global warming

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14
Q

Write an equation that desulfurises flue gas

A

CaCO3 + SO2 + 1/2 O2 —> CaSO4 + CO2

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15
Q

How do greenhouse gases contribute to global warming?

A

They trap infrared radiation in the atmosphere
Atmosphere heats up = global warming

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16
Q

Define carbon neutral activities

A

Activities that produce no net carbon dioxide emissions

17
Q

Explain the 3 stages of free radical substitution

A
  1. Initiation = breaking halogen bond to form free radicals
  2. Propagation = products formed but free radicals remain
  3. Termination = free radicals removed, stable products formed
18
Q

What conditions are needed for a free radical chlorine atom?

A

Presence of UV light

19
Q

Write the free radical substitution of methane with chlorine to make CH3Cl

A

Initiation:
Cl2 —> 2 Cl* (presence of UV light)
Propagation:
Cl* + CH4 —> HCl + CH3
CH3 + Cl2 —> CH3Cl + Cl
Termination:
CH3 + Cl —> CH3Cl
2Cl
—> Cl2
*CH3 + *CH3 —> CH3CH3

20
Q

How do chlorine free radicals catalyse the decomposition of O3?

A

Cl2 —> 2 Cl* (presence of UV light)
Cl* + O3 —> ClO* + O2
ClO* + O3 —> Cl* + 2 O2
Overall : 2 O3 —> 3 O2