Organic Chemistry Flashcards

1
Q

Define: Hydrocarbon

A

Compounds that only contain Hydrogen and Carbon atoms only

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2
Q

Define: Saturated

A

Contain maximum number of hydrogen for given number of carbon

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3
Q

Define: Unsaturated

A

The presence of the double bond mean they don’t have as many hydrogen

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4
Q

Formula for Alkane

A

Cn H2n+2

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5
Q

Formula for Alkene

A

Cn H2n

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6
Q

Homologous series

A

Similar structural and Chemical properties, due to similar bonding
General Formula

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7
Q

Alkane/Alkene physical trends

A

1,2,3,4 - Carbon - Gasses

5,6,7,8 - Carbon - Liquids

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8
Q

Alkane Combustion

A

Burn in oxygen

Enough they will give carbon dioxide and water

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9
Q

Incomplete combustion

A

Not enough oxygen

Carbon monoxide/carbon (soot) produced instead of CO2

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10
Q

Why is CO poisonous?

A

Combines with haemoglobin instead of oxygen

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11
Q

Substitution reaction

A

Alkane is substituted by a different atom, like in the reaction with bromine

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12
Q

Test for C=C

A

Shake organic compound with bromine water and the orange water is decolourised. Same for gas, but bubble through the water

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13
Q

Alcohols

A

Contain a -OH group onto the carbon chain

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14
Q

Ethanol by Fermentation

A

Yeast is added to starch and left in warm (30-40*C)
Absence of air.
Enzymes convert sugar into ethanol and CO2

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15
Q

Ethanol by hydration of Ethene

A

Ethene is passed over steam with Phosphoric acid Catalyst

300*C, 60-70 atm. Unreacted material is recycled

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16
Q

Dehydration of ethanol to produce ethene

A

Ethanol is passed over hot aluminium catalyst

17
Q

Pros/Cons of Hydration of Ethene

A

Pros - Fast and continuous process, Makes pure ethanol

Cons - High amounts of energy, Non-Renewable

18
Q

Pros/Cons of Fermentation

A

Pros - Renewable, Doesn’t require much energy

Cons - Batch process is slow, Impure ethanol

19
Q

Crude Oil

A

Finite, Mixture of hydrocarbons

20
Q

Properties of Hydrocarbons

A

As chains increase: Boiling points increase
Liquids become less volatile
Liquids flow less easily
Bigger hydrocarbons burn less easily

21
Q

Separating Crude oil

A

Oil is passed into a fractionating column, cooler at top than bottom. Boils, quickly then condenses at certain point to be tapped off

22
Q

Crude oil column at top/at bottom

A

Top going down less volatile e.g refinery gasses most

Bottom going up less viscous e.g fuel oil

23
Q

The 6 fractions

A

Bitumen, Fuel Oil
Diesel Oil, Kerosine
Gasoline, Refinery Gasses

24
Q

Uses for Refinery gasses, Gasoline, Kerosine

A

Refinery Gasses - Domestic heating/cooking
Gasoline - Petrol
Kerosine - Aircraft fuel

25
Uses for Diesel oil, Fuel oil, Bitumen
Diesel oil - Busses, Lorries, some cars Fuel oil - Ships boilers/industrial heating Bitumen - Road making
26
Problems with fractions
Amounts depend on hydrocarbons | Unreactive make into reactive
27
Cracking
Large hydrocarbons are converted into smaller ones, that have more demand
28
How Cracking works
Fraction heated to give gas, then passed over silicon dioxide and aluminium oxide catalyst at 600-700*C. A mixture of single and double bonds could form.
29
Addition polymerisation
Double bond is broken and electrons are used to join neighbouring molecules
30
Polymerisation
The joining up of monomers to make polymers
31
Condensation reaction
When two monomers combine a small molecule is lost. The monomers retain their bonds.