aldehydes and ketones Flashcards
functional group and naming of aldehydes
CHO functional group ending, ending in -al e.g. ethanal
functional group and naming of ketones
CO functional group in the middles, ending in -one, e.g. propanone
oxidation of aldehydes
aldehydes are readily oxidised into carboxylic acids due to acidified potassium dichromate and dilute sulfuric adic, when heated under refulx
observation when aldehydes are oxidised
colour change from orange to green and chromium is orange but reduced to green Cr3+
fehlings test
add fehlings solution and heat gently.
only aldehydes will be oxidised into carboxylic acids. blue to red precipitate
tollens test
tollens reagent added and heat gently.
only aldehydes are oxidised to carboxylic acids.
a silver mirror will form around the test tube
reduction of carbonyls
aldehydes are reduced to primary alcohols.
ketones are reduced to secondary alcohols.
NaBH4 or LiAlH4 in aq ethanol.
nucleophilic addition mechanism
addition of HCN to carbonyls
form hydroxynitrile.
KCN reagent and dilute H2SO4
room temp + pressure
nucleophilic addition
harm of HCN/KCN
HCN is not used as it is a toxic gas. and does not fully ionise as it is a weak acid
KCN is still toxic but will completely ionise as there is a greater CN- ion
how does nucleophilic addition result in a racemic mixture
addition of HCN to aldehydes and ketones when the planar carbonyl group is approached equally from both sides by HCN, as enantiomers are formed.