Aldehydes are named by replacing the -e ending of the corresponding alkane with -al . It is not necessary to specify the position of the aldehyde group, since it occupies the end of the chain (locant 1).
When the string contains two aldehyde functions, the suffix -dial is used.

aldehydes ketones nomenclature 01

[1] 4,4-Dimethylpentanal

[2] Pent-4-enal

[3] Hexanodial

Aldehydes and ketones can be prepared by oxidation of alcohols, ozonolysis of alkenes, hydration of alkynes, and Friedel-Crafts acylation as major methods.

a) Ozonolysis of alkenes: Alkenes break down with ozone to form aldehydes and/or ketones. If the alkene has vinyl hydrogens it gives aldehydes. If it has two carbon chains it forms ketones.

Aldehydes and ketones react in an aqueous acid medium to form hydrates. The mechanism consists of three stages. The first and fastest is the protonation of carbonyl oxygen. This protonation produces an increase in polarity on the carbon and favors the attack of the nucleophile. In the second stage, the water attacks the carbonyl carbon, it is the slow stage of the mechanism. In the third stage, oxygen deprotonation occurs, forming the final hydrate.

Hemiacetals are formed by reacting one equivalent of alcohol with the carbonyl group of an aldehyde or ketone. This reaction is acid catalyzed and is equivalent to the formation of hydrates.

Aldehydes and ketones react with alcohols under conditions of acid catalysis, forming hemiacetals in a first stage, which later evolve by reaction with a second equivalent of alcohol to acetals.

1,2- and 1,3-diols react with aldehydes and ketones to form cyclic acetals. The equilibria are shifted towards the final product by removing the water formed by azeotroping with benzene or toluene.

 Acetals can be used, due to their stability, as carbonyl protecting groups. The acetal is an ether, very stable in basic media, although it breaks in the presence of acidic media. In many synthesis processes, the carbonyl group is incompatible with the reagent used. In these cases it must be protected to prevent it from reacting. The instability of the acetal in an acidic medium can be used to deprotect the carbonyl.

Let's see some examples:

The reaction of aldehydes or ketones with primary amines generates imines . The reaction is favored in a slightly acid medium (pH=4.5).

oximes are obtained by reaction of aldehydes or ketones and hydroxylamine in a weakly acid medium. The mechanism is analogous to that of imine formation.


The hydrazones [3] are obtained by reaction of aldehydes or ketones [1] with hydrazine [2]. As in the case of imines and oximes, it requires pH=4.


semicarbazones are obtained by reaction of aldehydes or ketones with semicarbazide . Let's see an example:


It is a specific analytical test for aldehydes and ketones. carbonyls react with 2,4-Dinitrophenylhydrazine forming phenylhydrazones which precipitate yellow. The appearance of a precipitate is an indicator of the presence of carbonyls in the medium.


Enamine synthesis

As we saw in previous sections, the condensation of primary amines with aldehydes and ketones generates imines. In this section we will study the condensation of carbonyls with secondary amines that give enamines.


Enamine formation mechanism

After the initial attack of the secondary amine on the carbonyl, water is removed, forming the double bond between the carbonyl carbon and the alpha of the starting carbonyl.

Step 1. Protonation of the carbonyl


Step 2. Nucleophilic attack of the secondary amine


Stage 3. Acid-base balance


Stage 4. Loss of water


Stage 5. Elimination



Steric hindrances make the least substituted enamines the most stable


Cyanohydrins are formed by reaction of aldehydes or ketones with hydrocyanic acid and are compounds that contain a cynane and a hydroxy group on the same carbon.


The Wittig reaction employs phosphorus ylides [2] to transform aldehydes and ketones[1] in alkenes [3]. Triphenylphosphine oxide [4] is obtained as a by-product .


The ketone reaction with peracids produces esters . The oxygen of the peracid is inserted between the carbonyl carbon and the alpha carbon of the ketone. This reaction was described by Adolf von Baeyer and Victor Villiger in 1899.