carboxylic acids & derivatives [O2] PAPER 2 Flashcards

1
Q

general structure of a carboxylic acid?

A
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2
Q

esterification/ester hydrolysis reaction and conditions?

A

• alcohol + carboxylic acid ⇌ ester + water
• above the other way round = ester hydrolysis (in acidic conditions)
• concentrated strong acid catalyst, e.g. H2SO4

e.g.

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3
Q

saponification reaction?

A

• ester + alkali → salt of carboxylic acid + alcohol
• this is ester hydrolysis in alkaline conditions

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4
Q

common uses of esters?

A

• food flavourings
• perfumes
• solvents
• plasticisers

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5
Q

structure of glycerol (propan-1,2,3-triol) ?

A
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6
Q

Vegetable oils and animal fats are naturally occurring esters of glycerol.

Reaction that glycerol undergoes with three fatty acids (long C chain carboxylic acids) to form a triglyceride ester?

A
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7
Q

production of biodiesel reaction?

A

• transesterification
• lipid + methanol → 3 methyl esters of fatty acids + glycerol
• catalyst needed

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8
Q

saponification of a lipid?

A

lipid + 3KOH → 3 salts of fatty acids + glycerol

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9
Q

general structure and naming of an ester?

A

red = carboxylic acid
yellow = alcohol

[alcohol]yl [carboxylic acid]oate

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10
Q

general structure of an acid anhydride?

A
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11
Q

general structure of an acyl chloride?

A
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12
Q

name and outline the mechanism for the acylation of R—OH using R—COCl.

A

nucleophilic addition-elimination

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13
Q

name and outline the mechanism for the acylation of R—NH2 using R—COCl.

A

nucleophilic addition-elimination

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14
Q
A
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15
Q

Separate samples of each isomer are warmed with ethanoic acid and a few drops of concentrated sulfuric acid. In each case the mixture is then poured into a solution of sodium hydrogencarbonate.
Identify the isomer(s) that would react with ethanoic acid.
Suggest a simple way to detect if the ethanoic acid reacts with each isomer.
Give a reason why the mixture is poured into sodium hydrogencarbonate solution.

A

• P, Q, R, S
• sweet smelling liquid
• to react with excess acid

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16
Q
A
17
Q
A
18
Q
A