2.4 esters, fats and oils Flashcards

1
Q

What is the functional group of an ester?

A

ester link

-COO-

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2
Q

What are 3 uses of esters?

A
  • flavourings
  • fragrances
  • solvents for non-polar compounds that do not dissolve in water
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3
Q

What reaction forms an ester and what are the reactants?

A

condensation reaction between an alcohol and a carboxylic acid

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4
Q

What is a condensation reaction?

A

two molecules are joined together with the elimination of a small molecule

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5
Q

When an ester is formed by the reaction between a hydroxyl group and a carboxyl group, what small molecule is eliminated?

A

water

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6
Q

What can esters be hydrolysed to produce?

A

an alcohol and a carboxylic acid

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7
Q

What is a hydrolysis reaction?

A

a molecule reacts with water to break down into smaller molecules.

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8
Q

What family are edible fats and edible oils a part of?

A

esters

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9
Q

What is the systematic name for glycerol?

A

propane-1,2,3-triol

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10
Q

How are edible fats and edible oils formed?

A

formed in the condensation reaction of glycerol and three fatty acid molecules

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11
Q

What are long carbon chain, straight chain carboxylic acids called?

A

fatty acids

-they can be saturated or unsaturated

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12
Q

What is the difference is melting points of edible oils and edible fats?

A

edible oils have lower melting points than edible fats

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13
Q

Why do edible oils have lower melting points than edible fats?

A
  • double bonds in fatty acid chains prevent oil molecules from packing closely together
  • the greater the number of double bonds present, the weaker the London dispersion forces
  • the greater the degree of unsaturation, the lower the melting point
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14
Q

How do you test for unsaturated compounds and how does it work?

A
  • unsaturated compounds quickly decolourise bromine solution
  • the bromine molecules add across the carbon-carbon double bonds in an addition reaction
  • oils with a higher degree of unsaturation will require a higher volume of bromine solution than oils with a lower degree of unsaturation
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15
Q

Name 2 reasons why fats and oils are important

A
  • they are a concentrated source of energy

- essential for the transport and storage of fat-soluble vitamins in the body (due to their non-polar structure)

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16
Q

What is produced in the hydrolysis of edible fats and oils?

A
  • 3 fatty acid molecules

- 1 glycerol molecule

17
Q

Will fats or oils decolourise bromine solution?

A

oils as they are unsaturated molecules

18
Q

How are esters named?

A

-the first part of the name which ends in -yl comes from the alcohol
-the second part of the name which ends in -oate comes from the acid
ethanol+methanoic acid
–>ethyl methanoate

19
Q

Why do esters have a lower boiling point than carboxylic acids and alcohols and why can they not dissolve in water?

A

they do not contain a hydroxyl group. therefore esters cannot form hydrogen bonds to neighbouring ester molecules

  • less energy needed to separate molecules
  • non polar
20
Q

What type of ester are edible fats and edible oils?

A

triester

-containing three ester links

21
Q

Why is glycerol so viscous and have a high boiling point compared to other alcohols?

A
  • it has three -OH groups

- allows the glycerol molecules to form more hydrogen bonds between molecules than alcohols with only a single -OH group

22
Q

explain the difference between how fats are formed and how oils are formed?

A
  • fats are formed from saturated fatty acids

- oils are formed from unsaturated fatty acids

23
Q

What is another name for fats and oils?

A

triglyceride

24
Q

Explain the packing of edible fats

A
  • the efficient packing
  • allows for the London dispersion forces to hold the fat molecules together
  • these are greater between fat molecules than between oil molecules because of this efficient packing.
  • this means that it will take more energy to separate fat molecules and so the melting point will be higher than oils
  • solid at room temperature
25
Q

Explain the packing of edible oils

A
  • the double bonds cause the molecules to have a distorted structure, which makes it difficult for them to pack closely together
  • this results in fewer London dispersion forces between oil molecules
  • it therefore takes less energy to break apart the oil molecules
  • meaning that oils have a lower melting point than fats
26
Q

What is the catalyst used when producing an ester?

A

concentrated sufuric acid

27
Q

What is formed during the hydrolysis of an ester?

A

alcohol + carboxylic acid

28
Q

What are 2 observations that would show you have an ester?

A
  • layers

- smell

29
Q

Where does an ester link break during hydrolysis?

A

between the carbon of the carboxylic acid and the oxygen

  • H is added to the alcohol
  • OH is added to the carboxylic acid
30
Q

Fats and oils belong to which family of compounds?

A

esters

31
Q

What is the catalyst used during esterification?

A

concentrated sulphuric acid

32
Q

why would you use a condenser during esterification?

A

to condense any vapours or reactants/products which evaporate