4(e, f, g, h) Flashcards

1
Q

State the functional group for an Alcohol.

A

-OH

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2
Q

How is ethanol oxidised by the air in presence of microbes?(Give an example)(2)

A

Ethanol can be oxidised in the air through the help of microbes such as yeast or bacteria. Ethanol forms ethanoic acid, C(H3)COOH.
For example in wine, ethanol is oxidised to form vinegar.

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3
Q

How is ethanol oxidised by heating with potassium dichromate(IV) in dilute sulphuric acid?(3)

A

Potassium dichromate acts as an oxidising agent. Ethanol is added to potassium dichromate solution while it is heated.
Solution turns from yellow to green. Green colour indicates presence of Cr3+ ions.
Ethanol forms ethanoic acid, C(H3)COOH.

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4
Q

Describe how ethanol can be made by fermentation?(4)

A

Yeast is added to sugar solution and left about 30 celsius in anaerobic conditions for several days.
Enzymes convert the sugar into ethanol and carbon dioxide. This is called fermentation.
If the temperature was any greater than 40 celsius the enzymes would denature and too cool would be slow.
There must be no air so that the enzymes produce carbon dioxide and ethanol instead of carbon dioxide and water.

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5
Q

Why can fermentation ethanol never be pure?

A

Yeast is killed by more than about 15% of alcohol in the mixture and so it is impossible to make pure alcohol from fermentation alone.
However the alcohol can be purified by fractional distillation.

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6
Q

What are the advantages and disadvantages of Fermentation ethanol?(4)

A

+Renewable, made from sugar cane, sugar beet or corn
+Uses gentle temperatures and atmospheric pressure
-Batch process: everything mixed and then left for a few days which is inefficient
-Very impure ethanol
-Slow; each batch can take days

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7
Q

What are the advantages and disadvantages of Hydration ethanol?(4)

A

+Continuous flow produced, a stream of reactants constantly passed over; very effective
+Quick
+Very pure ethanol
-Uses high temperatures and pressures, therefore requiring more energy
-Finite no-renewable resources

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8
Q

Describe how ethanol can be made by the hydration of ethene? (3)

A

Ethene reacting with steam at 300 celsius and 60-70 atmospheres of pressure.
The catalyst is phosphoric acid.
Only small portion of the ethene reacts but the unreacted ethene is recycled through the process.

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9
Q

State the functional group for a carboxylic acid.

A

-COOH

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10
Q

How does dilute ethanoic acid react with magnesium?(2)

A

Lots of fizzing to produce a salt and hydrogen. The salt formed is magnesium ethanoate which is soluble in water and therefore the final solution is colourless.
((CH3)COO)2MG + H2

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11
Q

How does ethanoic acid react with carbonates?

A

Lots of fizzing to produce a salt, carbon dioxide and water.

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12
Q

State the functional group for an ester.

A

-COO-

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13
Q

How do ethanoic acid and ethanol react to form an ester?(3)

A

Heating a mixture of ethanoic acid and ethanol with a few drops of sulphuric acid, produces ethyl ethanoate.
This type of reaction is called esterification or a condensation reaction.
This reaction is also reversible so to maximise the produce of ethyl ethanoate, pure ethanol and ethanoic acid are often used.

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14
Q

What are some uses of esters?(3)

A

Small esters for example ethyl ethanoate are used in solvents, but the majority of esters are used in food flavourings and perfumes.
Esters are volatile liquids which means that they turn into vapour easily.
The typical smell in certain fruits is due to naturally occurring esters.

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15
Q

Define polymerisation.

A

Polymerisation is the joining up of lots of monomers(little particles) to make one polymer(big molecule.
Molecules simply add onto each other without anything else being formed, this is called addition polymerisation.

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16
Q

What are some uses for Polyethene or Polythene?(3)

A

Polythene has two types: low density polythene (LDPE) and high density polythene (HDPE).
LDPE is used mainly as thin film to make polythene bags. It is flexible but not very strong.
HDPE is used to make plastic in milk bottles because it is stronger and rigid.

17
Q

What are some uses for Polypropene?(2)

A

Polypropene little bit stronger than polythene. Used in crates and ropes.
Something with a recycling mark PP is made of polypropene.

18
Q

What are some uses for Polychloroethene?(2)

A

Polychloroethene or PVC has many uses. It is quite strong and so is used for water pipes or windows.
It can also be made flexible by adding plasticisers which makes it useful for clothes and sheet floor coverings.PVC doesn’t conduct electricity either.

19
Q

What are some uses for Polytetrafluoroethene?

A

PTFE is used for non stick coating for pots and pans. It is very unreactive because of the strong C-F bonds.

20
Q

Why do addition polymers take long to break down in the environment?(2)

A

They have strong covalent bonds which renders them inert at ordinary temperatures.
They are non-biodegradable so they can’t be broken down by bacteria.

21
Q

What are some solutions to disposing addition polymers?(4)

A

Landfill, which produces no greenhouses gases or toxic gases and is cheap.
However landfill is ugly, noisy and uses large areas of land.
Incineration is the other method which requires little space and produces heat or electricity for domestic uses.
However incineration is expensive to build, produces greenhouse gases and the ash produces still has to be disposed of in landfill.

22
Q

What are the two types of monomers in condensation polymerisation?(3)

A

The first is a diol; alcohol molecules with one -OH at each end.
The second is a dicarboxylic acid, a carboxylic molecule with one -COOH at each end.
When one diol and one dicarboxylic acid molecule form together H2O is removed to make a polymer.

23
Q

Why are there environmental issues with condensation polymers?(3)

A

Condensation polymers are more reactive than addition polymers because of the ester linkage. However this could still take hundreds of years to break down.
Biopolyesters are polyesters that have been developed to be more biodegradable.
These biopolyesters are made from lactic acid which can be acquired from corn starch.