Aldehydes and Ketones Flashcards

1
Q

why is a primary alcohol heated under distillation to prepare an aldehyde

A
  • distillation seperates the aldehyde from the oxidising agent
  • and hence prevents further oxidation of the aldehyde to a carboxyllic acid
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2
Q

describe a chemical test, which can be used to distinguish between an aldehyde and a ketone

A

Add tollens reagent - if a silver mirror is produced then its an aldehyde, if not its a ketone

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3
Q

what happens if an aldehyde or ketone undergoes nucleophilic addition

A
  • a (K)CN- nucleophile attacks them
  • a hydroxynitrile is formed
  • can give rise to optical isomers
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4
Q

suggest a reason why KCN is used instead of HCN

A
  • HCN and KCN are toxic gases
  • HCN is weak/ KCN dissocited better than HCN
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5
Q

what are aldehydes and ketones reduced to

A
  • aldehydes are reduced to primary alcohols
  • ketones are reduced to secondary alcohols
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6
Q

what are the reagents and conditions of nucleophilic addition for reduction

A

reagents: sodium tetrahydridoborate, NaBH4

conditions: solvent is water, warm aqeuous solution

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7
Q

why is NaBH4 a suitable reducing agent carbonyl compounds

A

the BH4- ions from NaBH4, provides hydride ions, :H-, which act as a nucleophile

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8
Q
A
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