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Lec-1, Ch12 Class 12
Lec-1, Ch12 Class 12
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Aldehyde
prefix- oxo or
formyl
suffix- al
IUPAC Name
Alkanal
Ketone
prefix- oxo
suffix- one
IUPAC Name
Alkan-one
1. By oxidation of alcohols By dehydrogenation of alcohols
From Hydrocarbons
Ozonolysis of Alkynes
Hydration of Alkynes:
Catalyzed by mercury(II) salts, water can be added to alkynes according to the
Markovnikov’s rule. This reaction yields enoles which tautomerize to the carbonyl
compounds. Ethyne yields acetaldehyde; terminal alkynes produce methyl ketones.
BaSO4/S OR
Quinoline Poison
the catalyst and
prevents reduction
of aldehyde into 1o
Preparation of Ketones from Acyl Chlorides alcohol
Acyl chlorides upon treatment with Dialkyl cadmium (R2Cd) form ketones.
Ketones can be prepared by Reaction of cyanides with RMgX
From Esters
From Geminal Dihalides
Friedel–Crafts acylation involves the acylation of aromatic rings using acylating agents like
acyl chlorides and acid anhydrides in the presence of catalyst anhydrous AlCl3
Aldehydes and ketones are polar in nature.
1.
2.
Chemical Properties of Aldehydes and Ketones
1.
2.
3.
4.
5.