carboxylic acids Flashcards

1
Q

suggest how anti-bumping granules prevent bumping during reflux

A
  • prevents vigorous uneven boiling
  • by making small bubbles form instead of large bubbles
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2
Q

suggest why an excess of sodium hydroxide is uses in hydrolysis of esters

A
  • to ensure the ester is completely hydrolysed
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3
Q

suggest why an electric heater is used rather than a bunsen burner in this hydrolysis

A
  • organic compounds are flammable
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4
Q

suggest why reflux is used in this hydrolysis

A
  • reflux prevents reacta vapour from escaping
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5
Q

suggest why sodium benzoate is soluble in cold water but benzoic acid is insoluble in cold water

A
  • sodium benzoate is ionic
  • benzoic acid is insoluble because the benzene ring is non polar
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6
Q

describe the method the student should use to purify the benzoic acid

A
  • dissolve crude product in hot solvent
  • of minimum volume
  • filter ( hot to remove insoluble impurities)
  • cool to recrystallise
  • filter under reduced pressure with Buchner
  • wash with cold solvent and dry
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7
Q

give the equation for acid + metal

A

acid + metal > salt + hydrogen

2CH3COOH + 2Na > 2CH3COONa + H2

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8
Q

give the equation for acid + alkali

A

acid + alkali > salt + water

CH3COOH + NaOH > CH3COONa + H2O

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9
Q

give the equation for acid + carbonate

A

acid + carbonate > salt + water + carbon dioxide

2CH3COOH + Na2CO3 > 2CH3COONa + H2O + CO2

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10
Q

what is the functional test for carboxylic acids ?

A
  • reaction of carboxylic acids with solid metal carbonate produces effervescence caused by production of CO2
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11
Q

what happens when carboxylic acids react with alcohols in presence of a strong acid catalyst

A
  • esters and water is formed
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12
Q

give the general equation for acid + alcohol

A

acid + alcohol >< ester + water

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13
Q

what are the downsides of esterification

A
  • reaction is reversible
  • the reaction is slow and needs heating under reflux
  • low yields are achieved
  • acid catalyst is needed
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14
Q

what are the downsides of esterification

A
  • reaction is reversible
  • the reaction is slow and needs heating under reflux
  • low yields are achieved
  • acid catalyst is needed
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15
Q

what are the main uses of esters

A
  • perfumes and flavourings
  • solvents for polar organic substances
  • uses for plasticisers for polymers
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16
Q

what are the two ways esters can be hydrolysed and split up

A
  • heating with acid
  • sodium hydroxide
17
Q

what are the conditions for with acid

A
  • dilute acid (HCL)
  • heat under reflux
18
Q

what are the conditions for with sodium hydroxide

A
  • dilute sodium hydroxide
  • heat under reflux
19
Q

why is the reaction of esters with sodium hydroxide not reversible

A
  • carboxylic acid salt product is the anion of the carboxylic acid
  • anion is resistant to attack by weak nucleophiles such as alcohols