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Chemistry LibreTexts

23.1 Carbonyl Condensations - The Aldol Reaction

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  • Page ID
    91014
  • Objectives

    After completing this section, you should be able to

    1. write a general mechanism for carbonyl condensation reactions.
    2. write an equation to illustrate the aldol condensation reaction.
    3. identify the product formed when an aldehyde or ketone having an alpha‑hydrogen atom is treated with base in a protic medium.
    4. identify the aldehyde or ketone, and other reagents required to produce a given β‑hydroxy carbonyl compound by an aldol reaction.
    5. determine whether a given aldehyde or ketone will undergo an aldol reaction.
    6. write the detailed mechanism of the aldol reaction.

    Key Terms

    Study Notes

    It is important that you understand the general mechanism of carbonyl condensation described in this section: once you grasp this mechanism, you will see that all the reactions that follow are very similar.

    The aldol reaction is sometimes referred to as the aldol condensation. However, a condensation reaction is often regarded as a reaction in which two molecules join together with the elimination of a molecule of water (or some other compound of low molar mass). Thus, the aldol reaction described here is not a true condensation; the true aldol condensation is described later, in Section 23.3. It is perhaps unfortunate that the reactions discussed in this unit are all described as condensation reactions whether or not water is eliminated.

    The term “aldol” (from "aldehyde alcohol") is used both to describe the specific compound 3‑hydroxybutanal:

    3-hydroxybutanal

    and to describe β‑hydroxy aldehydes in general.

    A useful carbon-carbon bond-forming reaction known as the Aldol Reaction is yet another example of electrophilic substitution at the alpha carbon in enolate anions. The fundamental transformation in this reaction is a dimerization of an aldehyde (or ketone) to a beta-hydroxy aldehyde (or ketone) by alpha C–H addition of one reactant molecule to the carbonyl group of a second reactant molecule. Due to the carbanion like nature of enolates they can add to carbonyls in a similar manner as Grignard reagents. For this reaction to occur at least one of the reactants must have α hydrogens. 

    General Aldol reaction

    Going from reactants to products simply

     

    1a.jpg

    Example 23.1.1: Aldol Reactions

     

    Aldol Reaction Mechanism

    Step 1: Enolate formation

    1b.jpg

    Step 2: Nucleophilic attack by the enolate

    4.jpg

    Step 3: Protonation

    5.jpg

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