organic chemistry paper 2 Flashcards

1
Q

what are the conditions needed to oxidise ethanol to ethanoic acid in a lab?

A
  • potassium dichromate (oxidising agent)
  • sulfuric acid

the colour change is orange to green

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2
Q

explain the proccess of microbial oxidation

A

some organisms use oxygen in the air to oxidise alcohols

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3
Q

how can ethanol be produced?

A
  • ethene + steam
  • fermentation
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4
Q

describe the conditions to react ethene with steam

A
  • 300 degrees
  • pressure 60-70 atm
  • phosphoric acid catalyst
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5
Q

explain why ethene and steam is an addition reaction

A

water is added to the molecule

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6
Q

what are the advantages of producing ethanol from ethene?

A
  • cheap
  • produces pure ethanol
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7
Q

What is a disadvantage of producing ethene from steam?

A

crude oil is a non-renewable source so will soon become very expensive

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8
Q

explain how ethanol can be produced by fermentation

A

sugar e.g. glucose is converted to ethanol using yeat due to enzymes they use

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9
Q

explain the conditions required to produce ethanol by fermentation

A
  • 30 degrees - if too hot the yeast denatures and the reaction stops
  • anaerobic conditions otherwise ethanoic acid will be produced
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10
Q

what are some advantages of producing ethanol via fermentation?

A
  • lower energy cost
  • sugar cane is a renewable source
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11
Q

what are some disadvantages of producing ethanol via fermentation?

A
  • ethanol produced is impure so more expensive
  • slower proccess
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12
Q

give 2 uses of ethanol

A
  • fuels
  • solvents e.g. in perfume
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13
Q

what is produced when a carboxylic acid reacts with a metal carbonate?

A

salt + water + carbon dioxide

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14
Q

what is produced when a carboxylic acid reacts with a metal?

A

salt + hydrogen

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15
Q

i.e. which food

where is ethanoic acid found?

A

vinegar

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16
Q

How is an ester produced?

A

alcohol + carboxylic acid

17
Q

explain how to name an ester

A

the first part e.g. ethyl is from the alcohol used and the second part (anoate) is from the carboxylic acid used

18
Q

explain why esters are used in perfumes

A

they are volatile and have pleasant smells

19
Q

explain why addition polymers are difficult to dispose of

A
  • they are inert are the carbon-carbon bonds are difficult to break
  • meaning that it takes a long time for them to biodegrade so take up space in landfills
  • when burned they release toxic gases that are harmful to humans
20
Q

explain why polyesters are condensation polymers

A

for each new bond in the polymer that forms, a molecule of water is lost

21
Q

which monomers are needed to produce a condensation polymer?

A

dicarboxylic acids are diol monomers

the ‘di’ signifies two functional groups

22
Q

give an example of a diol

A

ethanediol

23
Q

give an example of a dicarboxylic acid

A

ethanedioic acid

24
Q

give an example of a polyester

A

poly(ethyl ethanoate)

25
Q

what property of polyesters reduces their pollutant effect on the environment?

A

they are biodegradable