English

Explain aldol condensation reaction in detail. - Chemistry

Advertisements
Advertisements

Question

Explain aldol condensation reaction in detail.

Long Answer
Advertisements

Solution

  1. Aldehydes containing at least one α–hydrogen atom undergo a reaction in presence of dilute alkali (dilute NaOH, KOH, or Na2CO3) as the catalyst to form β-hydroxy aldehydes (aldol). This reaction is known as the aldol reaction.
  2. Formation of aldol is an addition reaction.
  3. Aldol formed from aldehyde having α-hydrogens undergoes subsequent elimination of water molecule on warming. This gives rise to α,β-unsaturated aldehyde.
  4. The overall reaction is called aldol condensation. It is a nucleophilic addition-elimination reaction.
  5. The reaction can be given as,
    \[\begin{array}{cc}
    \ce{\underset{\text{Aldehyde}}{2R - CH2 - CHO} ->[aq.NaOH] R - CH2 - CH - CHR - CHO}\\
    \phantom{.......................}|\\
    \phantom{..........................}\ce{\underset{\text{Aldol}}{OH}}
    \end{array}\]
    \[\begin{array}{cc}
    \ce{R - CH2 - CH - CHR - CHO ->[-H2O][warm] \underset{\text{α,β-Unsaturated aldehyde}}{R - CH = CR - CHO}}\\
    |\phantom{.......................................}\\
    \ce{\underset{Aldol}{OH}}\phantom{.....................................}
    \end{array}\]
    e.g.
  6. Ketones containing at least two α-hydrogen also undergo aldol condensation reaction and give an α,β-unsaturated ketone.
    e.g.
shaalaa.com
  Is there an error in this question or solution?
Chapter 12: Aldehydes, Ketones and Carboxylic acids - Short answer questions (Type-II)

APPEARS IN

SCERT Maharashtra Chemistry [English] 12 Standard HSC
Chapter 12 Aldehydes, Ketones and Carboxylic acids
Short answer questions (Type-II) | Q 2

RELATED QUESTIONS

A compound 'A' of molecular formula C2H3OCl undergoes a series of reactions as shown below. Write the structures of A, B, C and D in the following reactions :


Write the products formed when CH3CHO reacts with the following reagents: CH3CHO in the presence of dilute NaOH


Which of the following compounds would undergo aldol condensation, which the Cannizzaro reaction and which neither? Write the structures of the expected products of aldol condensation and Cannizzaro reaction.

  1. Methanal
  2. 2-Methylpentanal
  3. Benzaldehyde
  4. Benzophenone
  5. Cyclohexanone
  6. 1-Phenylpropanone
  7. Phenylacetaldehyde
  8. Butan-1-ol
  9. 2, 2-Dimethylbutanal

How will you convert ethanal into the following compound?

Butane-1, 3-diol


How will you bring about the following conversion in not more than two steps?

Benzaldehyde to 3-Phenylpropan-1-ol


Complete the synthesis by giving missing starting material, reagent or product.

\[\begin{array}{cc}
\ce{C6H5CHO}\phantom{............}\\
\phantom{........}\ce{+\phantom{......}\ce{->[dil.NaOH][\Delta]}}\phantom{...}\\
\ce{CH3CH2CHO}\phantom{............}
\end{array}\]


Give reasons  Acetylation of aniline reduces its activation effect.


Write chemical equations of the following reaction : 

Propanone is treated with dilute Ba (OH)2-.


Write chemical equations of the following reaction :
Benzoyl chloride is hydrogenated in the presence of `"Pd"/(BaSO_4)`


Write a chemical equation for the following reaction: 
Propanone is treated with dilute Ba( OH)2.


Cannizaro’s reaction is not given by ______.


Compounds A and C in the following reaction are:

\[\ce{CH3CHO ->[(i) CH3MgBr][(ii) H2O] (A) ->[H2SO4, Δ] (B) ->[Hydroboration oxidation] (C)}\]


Why is there a large difference in the boiling points of butanal and butan-1-ol?


Compound ‘A’ was prepared by oxidation of compound ‘B’ with alkaline \[\ce{KMnO4}\]. Compound ‘A’ on reduction with lithium aluminium hydride gets converted back to compound ‘B’. When compound ‘A’ is heated with compound B in the presence of \[\ce{H2SO4}\] it produces fruity smell of compound C to which family the compounds ‘A’, ‘B’ and ‘C’ belong to?


Why are carboxylic acids more acidic than alcohols or phenols although all of them have hydrogen atom attached to a oxygen atom \[\ce{(-O-H)}\]?


Assertion: The α-hydrogen atom in carbonyl compounds is less acidic.

Reason: The anion formed after the loss of α-hydrogen atom is resonance stabilised.


Cross aldol condensation occurs between


Identify A and B from the following reaction:

\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{....................}\\
\phantom{}\ce{2CH3 - C = O ->[Ba(OH)2] A ->[Δ] B + H2O}
\end{array}\]


The major product of the following reaction is:


Assertion (A): The final product in Aldol condensation is always α, β-unsaturated carbonyl compound.

Reason (R): α, β-unsaturated carbonyl compounds are stabilised due to conjugation.


Identify A and B:


When acetaldehyde is treated with dilute NaOH, the following reaction is observed.

\[\begin{array}{cc}
\ce{2CH3 - CHO ->[dil.NaOH] CH3 - CH - CH2 - CHO}\\
\phantom{...............}|\\
\phantom{.................}\ce{OH}
\end{array}\]

  1. What are the functional groups in the product?
  2. Can another product be formed during the same reaction? (Deduce the answer by doing atomic audit of reactant and product).
  3. Is this an addition reaction or condensation reaction?

Write a note on the aldol condensation reaction of acetaldehyde.


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×