Carboxylic acids Flashcards

1
Q

describe acidity of carboxylic acids

A

weak acids but stronger than alcohol

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2
Q

why is carboxylic acid weak acid

A

electron withdrawing group C=O pulls electron towards itself
weakened C-OH bond
delocalisation spreads and ion is stable = lower charge density
stay dissociated

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3
Q

describe acidity of alcohol

A

electron withdrawing group and donating group present

high charge density at oxygen

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4
Q

colour change for acidified potassium manganate (VII)

A

purple to colourless

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5
Q

colour change of acidified potassium dichromate (VI)

A

orange to green

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6
Q

colour change and reaction of fehling’s

A

Cu2+ → Cu + (red precipitate)

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7
Q

colour change and reaction of tollen’s

A

Ag+ → Ag (silver precipitate)

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8
Q

which two acids produce water and carbon dioxide when oxidised

A

ethanedioic and methanoic

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9
Q

conditions for oxidising acids

A

warm
reflux
oxidising agent

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10
Q

how do you produce acyl chlorides (3)

A

with PCl5/PCl3 + heat/SOCl2

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11
Q

what are the products when acid + PCl5

A

acyl chloride + POCl3 + HCl

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12
Q

what are the products when acid + PCl3 + heat

A

acyl chloride + H3PO3

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13
Q

what are the products when acid + SOCl2

A

acyl chloride + SO2 + HCl

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14
Q

how do we extract acyl chloride out

A

fractional distillation

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15
Q

why are acyl chlorides more reactive

A

O=C-Cl causes carbon to be very positive and open to nucleophilic attack

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16
Q

rate in ease of hydrolysis
aryl chloride
acyl chloride
chloroalkane

A

acyl chloride > chloroalkane > aryl chloride

17
Q

reactions acyl chloride undergoes (3)

A

hydrolysis
reaction with alcohol group
reaction with amines

18
Q

type of reaction acyl chloride undergoes

A

addition-elimination

19
Q

benzoyl chloride + water

A

carboxylic acid

20
Q

Ethanoyl chloride + ethanol

A

→ (ester) ethyl ethanoate + HCl

21
Q

Ethanoyl chloride + sodium phenoxide ( + conditions)

A

→ phenyl ethanoate (ester) + NaCl

aq.NaOH + warm

22
Q

Ethanoyl chloride + ethylamine

A

→ N-ethylethanamide + HCl