Organic Chemistry Flashcards

(42 cards)

1
Q

Homologous series

A

Compounds that have a similar chemical structure and chemical properties

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2
Q

Organic compounds

A

Compounds consisting of carbon atoms most commonly covalently bonded to hydrogen, nitrogen, phosphorus or oxygen atoms

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3
Q

Hydrocarbon

A

Organic compound containing only hydrogen and carbon.

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4
Q

Functional group

A

Specific groups of atoms within a compound that affect the properties of the compound.

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5
Q

Alkanes

A

Saturated molecules - all carbons to carbon single bonds

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6
Q

Alkenes

A

Unsaturated molecules - contains at least one carbon-to-carbon double bond

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7
Q

Test for unsaturation

A

Bromine water will turn brown/orange to colourless if at least one carbon-carbon double bond is present

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8
Q

Alkane General Formula

A

CnH2n+2

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9
Q

Alkene General Formula

A

CnH2n

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10
Q

Alkene functional group

A

Carbon-carbon double bond

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11
Q

Haloalkane General Formula

A

CnH2n+1X

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12
Q

Haloalkane functional group

A

Halogen X

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13
Q

Isomers

A

Molecules that have the same molecular formula but a different structural formula.

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14
Q

Fractional Distillation

A

Crude oil is heated to vaporise the contents.

A tall fractionating column is fitted above the mixture.
The column is hot at the bottom and cool at the top.

As HC reach their BP, they rise, condense from gas to liquid and are tapped off.

Short HC reach BP first.

Longer HC remain as a liquid and are tapped off in liquid form.

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15
Q

Why do the longer hydrocarbon chains take more heat energy to change state from solid to liquid or liquid to gas?

A

The longer the chain, the stronger the dispersion forces there are between the molecules thus requiring more energy to break.

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16
Q

Viscosity

A

Viscosityis a measure of a fluid’s resistance to flow.

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17
Q

When the hydrocarbon goes through a state change of liquid to gas, which bonds are broken?

A

Weak intermolecular forces (dispersion) are broken when the hydrocarbon reaches its boiling point and transitions from liquid to a gas. The covalent bonds between the atoms do not beak. This would required a higher amount of energy.

18
Q

Difference in boiling point of small and larger hydrocarbons

A

Smaller the molecule the lower the boiling point because there are lesson intermolecular forces between the molecules.

And therefore, less energy required to break them.

19
Q

Crude oil

A

A dark, viscous substance extracted from the ground

20
Q

Hydrocarbons from short to long in crude oil and uses

A

Petroleum gas - heating and cooking
Gasoline - fuel for cars
Naphtha - plastic chemicals
Paraffin / Kerosene- fuel for planes
Diesel Oil - fuel in diesel engines e.g. trucks
Fuel Oil - home heating
Lubricating Oil - lubricants, waxes and polishes
Bitumen - road construction

21
Q

How is crude oil bad for the environment and what are alternatives?

A

Extraction through drilling: disrput ecosystems and cause spillage
Refineries: Air and water pollution
Finite resource

Alt.: Plant-based biomass e.g. corn or tree bark

22
Q

Cracking

A

Large hydrocarbon molecules can be broken down into smaller molecules using a catalyst.
Thermal decomposition

23
Q

Cracking Method

A

Heating mineral wool soaked in oil with a catalyst. Catalyst is heated first because oil is flammable. Contents vapourise

24
Q

Cracking Catalyst

A

Aluminium Oxide or Clay

25
Complete combustion
hydrocarbon is burned in excess oxygen hydrocarbon + oxygen → carbon dioxide + water
26
Incomplete combustion
hydrocarbon is burned in limited oxygen hydrocarbon + oxygen → carbon monoxide + water or hydrocarbon + oxygen → carbon + water
27
Substitution reaction
One atom is swapped with another atom. Alkanes undergo a substitution reaction with halogens in the presence of UV light.
28
Addition reaction (with halides, including conditions)
Double bond breaks and additional atoms are added.
29
Hydrogenation (addition reaction with H2, including conditions)
Alkene + hydrogen (150degreesC and Ni catalyst)→ alkane
30
Hydration (addition reaction with H2O, including conditions)
Alkene + water (steam) (phosphoric acid catalyst + 300degrees C) → alcohol
31
Ethanol production (including advantages and disadvantages) Fermentation of glucose
Fermentation of glucose: C6H12O6 (yeast catalyst) → C2H5OH + CO2 Advantages: Simple method and Uses renewable resources Disadvantages: Not a continuous process, slow reaction and produces low purity ethanol
32
Ethanol production (including advantages and disadvantages) Hydration
Ethene + steam C2H4 + H2O (g) → C2H5OH Advantages: Small-scale equipment, continuous process, reaction is fast and produces high purity ethanol Disadvantages: Uses non-renewable resources
33
Alcohol functional group
OH
34
Alcohol general formula
CnH2n+1OH
35
Carboxylic acid general formula
CnH2n+1COOH
36
Carboxylic acid functional group
COOH
37
Carboxylic acid name ends in ...
Name ends in -oic acid
38
Alkyl Halides
Organic compounds containing halogens are called alkyl halides (group 7 elements)
39
Polymerisation
The formation of a large molecule (polymer) from many monomer subunits.
40
Monomers
Monomer: small molecules that can join to form a polymer
41
Polymers
Polymer: large molecules built up from small units (monomers)
42
Why are hydrocarbons good fuels?
Release usable energy when burned.