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Aldol Condensation Reaction (Aldehyde)
It is a organic reaction between same type of carbonyl compounds(Ketone
/Aldehyde) in the presence of strong base to form β-hydroxy ketone or β-
hydroxy aldehyde product.
We can easily remember this reaction Aldol=Ald +ol
Aldehyde into oL(Alcohol)
Why Carbonyl compounds undergo aldol condensation reaction
Due to presence of α-hydrogen. The acidic property of α-hydrogen in
aldehydes and ketones is because of the high electron-withdrawing
capacity of the carbonyl group and resonance stabilization of the
conjugate base.
Example of Aldol Reaction in Aldehydes
H 3 C
C
H
O
+
H 3 C
C
H
O
N a O H
H 3 C
C
O H
H 2
C C
O
C H 3
H
A c e t a l d e h y d e A c e t a l d e h y d e
4 - H y d r o x y - p e n t a n - 2 - o n e
Reaction Mechanism
Step 1: Removal of α-hydrogen from the base
Carbanion
Step 2: The first step results in the formation of carbanion which
undergoes a nucleophilic addition reaction with the carbonyl group
present in the second molecule of the aldehyde (in this case ethanal).
The second step results in the formation of the condensation product.
Step 3: Protonation of alkoxide ion will occur due to
reaction with water.
Step 4: Heating of the aldol compound in the basic
solution will help in dehydrating the product to form α
β‐unsaturated aldehyde compound.
Upcoming Topics
1. Aldol Condensation in Ketonic Compounds
2. Cross Aldol Condensation Reaction
3. Cannizzaro Reaction
4. Wurth Reaction
5. Friedel-Crafts Reaction

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Aldol Condensation || with Mechanism || Aldehyde Chemical Rxn| ALDOL Reaction with Easy Mechanism

  • 1. Aldol Condensation Reaction (Aldehyde) It is a organic reaction between same type of carbonyl compounds(Ketone /Aldehyde) in the presence of strong base to form β-hydroxy ketone or β- hydroxy aldehyde product. We can easily remember this reaction Aldol=Ald +ol Aldehyde into oL(Alcohol) Why Carbonyl compounds undergo aldol condensation reaction Due to presence of α-hydrogen. The acidic property of α-hydrogen in aldehydes and ketones is because of the high electron-withdrawing capacity of the carbonyl group and resonance stabilization of the conjugate base.
  • 2.
  • 3. Example of Aldol Reaction in Aldehydes H 3 C C H O + H 3 C C H O N a O H H 3 C C O H H 2 C C O C H 3 H A c e t a l d e h y d e A c e t a l d e h y d e 4 - H y d r o x y - p e n t a n - 2 - o n e
  • 4. Reaction Mechanism Step 1: Removal of α-hydrogen from the base Carbanion
  • 5. Step 2: The first step results in the formation of carbanion which undergoes a nucleophilic addition reaction with the carbonyl group present in the second molecule of the aldehyde (in this case ethanal). The second step results in the formation of the condensation product.
  • 6. Step 3: Protonation of alkoxide ion will occur due to reaction with water.
  • 7. Step 4: Heating of the aldol compound in the basic solution will help in dehydrating the product to form α β‐unsaturated aldehyde compound.
  • 8. Upcoming Topics 1. Aldol Condensation in Ketonic Compounds 2. Cross Aldol Condensation Reaction 3. Cannizzaro Reaction 4. Wurth Reaction 5. Friedel-Crafts Reaction