Organic chemistry Flashcards

(48 cards)

1
Q

How are coal, oil and natural gas formed?

A

Formed as a result of heat and pressure

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2
Q

How is petroleum separated into smaller hydrocarbons?

A

Fractional distillation

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3
Q

Order of hydrocarbons in fractionating column

A
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4
Q

What is a fraction

A

A mixture of compounds with a similiar boiling point

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5
Q

What is refinery gas used for

A

Bottled gas

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6
Q

What is gasoline used for

A

Petrol

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7
Q

What is kerosene used for

A

Jet fuel

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8
Q

What is diesel used for

A

Train and car fuel

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9
Q

What is fuel oil used for

A

Central heating

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10
Q

What is bitumen used for

A

Road and roof tar

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11
Q

What is a homologous series

A

A family of hydrocarbons which have similiar features and chemical properties due to being in the same functional group

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12
Q

What test can be used to tell which is an alkane and which is an alkene

A

Bromine water -

Alkanes will be orange

Alkenes wil decolourise

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13
Q
A
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14
Q

What do all members of a homologous series have

A

Same general formula

Same functional group

Similiar chemical properties

Gradiation in their physical properties

Difference in molecular formula between one member and the next is CH2

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15
Q

What is a functional group

A

A group of atoms bonded in a specific arrangement which is responsible for the characteristic reactions of each member of a homologous series

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16
Q

What is a structural isomer

A

Compounds with the same molecular formula but different structural formula

There are two different types of structural isomer which are chain and position

In chain the structure of the carbon chain differs

In position the position of the functional group differs

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17
Q

example of chain isomer

A
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18
Q

example of position isomer

A
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19
Q

What are alkanes

A

Saturated hydrocarbons

Contain no double bonds

Colourless compounds which have a gradual change on their physical properties as the number of carbon atoms in the group increases

Generally unreactive compounds but they do ungo combustion reactions and can be cracked into smaller alkanes and react with halogens in the presence of light

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20
Q

What is the main component of natural gas

21
Q

Combustion of methane

22
Q

What is a substitution reaction

When do substitution reactions occur on alkanes

A

Substitution reaction - where one atom of one element/compound is swapped with an atom from another compound

Alkanes unergo substitution reactions with halogens in the presence of light

23
Q

What are alkenes

A

Alkenes are hydrocarbons which contain a double bond

They are unsaturated compounds

24
Q

How are alkenes and hydrogen made?

A

The catalyctic cracking of long alkane chains

25
What is catalyctic cracking?
The breakdown of less-useful longer hydrocarbon chains and shorter useful hydrocarbons
26
How is catalytic cracking conducted
Fractions containing large hydrocarbon molecules are heated at 600-700 degrees to vaporize them Vapours are then passed over a catalyst of silica and alumina This breaks the covalent bonds causing thermal decomposition The longer hydrocarbon chain has been broken up into shorter chains of alkenes and alkanes
27
Example of alkanes being cracked
Kerosene and diesel oil are often cracked to form petrol other alkenes and hydrogen
28
How does bromine water show that one is an alkane and the other an alkene?
Bromine water is an orange coloured solution of bromine When bromine water is shaken with an alkane, it remains orange as there no C=C bonds present; so the bromine remains in solution When bromine water is shaken with an alkene, it decoloursies due to the presence of a C=C bond The bromine atoms add across the C=C hence the solution no longer contains orange bromine water
29
What type of reaction occurs between an alkene and bromine water
An addition reaction
30
Example of an addition reaction
31
What is addition polymerisation
The joining of monomers to form addition polymers This only occurs in monomers containing C=C bonds
32
What occurs in addition polymerisation
One of the bonds in each double bond breaks and forms a bond with the adjacent monomer An example of an synthesized alkene monomer in poly-ethene
33
What is a hydrogenation reaction
When an alkene is reacted with H2 to form an alkane This reaction occurs at 150\*C using a nickel catalyst
34
Practical use of hydrogenation reaction
Turning vegetable oils into margerine for supermarkets
35
What are the conditions and products of alkene + steam
Conditions - 300\*C, 60-70atm, concentrated phosporic acid catalyst Alkene + water --\> alchahol This is called the hydration of alkene
36
What is an alchahol
Contains the -OH functional group
37
What is ethanol
An alchahol - C2H5OH Found in alchaholic drinks, used in cars as a solvent for fuel Ethanol burns in excess to form carbon dioxide and water
38
What are the two methods for the manufacture of ethanol
Hydration of ethene fermentation of glucose
39
How is the fermentation of glucose carried out (ethanol manufacture)
Sugar or starch is added in water and yeast is added Mixture ferments for a few days with no oxygen between the tempuratures 15 and 35\*C Yeast contains enzymes that break down the starch or sugar to glucose If the tempurature is too slow the reaction rate will be too low If the tempurature is too high the enzymes denature The yeast respires anaerobically to form CO2 and ethanol The yeast are killed off oncethe level of alchahol is 15%
40
Balanced equation of fermentation of glucose
41
Comparison of fermentation to hydration of ethene - hydration of ethene
Hydration of ethene - complex set up uses non-renewable resources fast rate of reaction produces pure ethanol No greenhouse gases produced Reaction conditions - high temp and pressure
42
Comparison of fermentation and hydration of ethene - fermentation
Simple equipment needed Uses re-newable resources Batch proccess - inefficient Very slow process Produces a dilute solution of alchahol which requires further processing
43
What is a carboxylic acid
The homologous series containing the functional group -COOH Colourless liquid Weak acids, typical acidic properties They react with alkaline solutions, turn blue litmus red, and form salts called ethanoates
44
Properties of ethanoic acid
Weak acid Dissociates slightly in water Equilibrium lies far to the left in ionization ethanoic acid reacts with more reactive metals, carbonates and hydroxides
45
How to make carboxylic acids - oxidation by fermentation
The microbial fermentation of alchahol will produce a weak solution of vinegar This occurs when a bottle of wine is opened as the bacteria in the air use the oxygen in the air to oxidise the ethanol in the wine The acidic, vinegary taste of opened wine is due to the production of ethanoic acid
46
Production of carboxylic acids - alchahols heated with potassium manganate
Alchahols are heated with potassium mangante in a vessel with a condenser attached to the top The condenser prevents the volatile alchahol from escaping from the reaction vessel as alchahols have low boiling points
47
How are esters made
By adding alchahols and carboxylic acids togeth
48
What are esters
Esters are compounds with the functional group R-COO-R Esters are sweet smelling oily liquids in food flavourings and perfumes