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प्रश्न
Identify A and B from the following reaction:
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{....................}\\
\phantom{}\ce{2CH3 - C = O ->[Ba(OH)2] A ->[Δ] B + H2O}
\end{array}\]
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उत्तर
\[\begin{array}{cc}
\phantom{..........}\ce{CH3}\phantom{..................}\ce{CH3}\phantom{.......}\ce{CH3}\phantom{....................}\ce{CH3}\phantom{......}\ce{CH3}\phantom{...........}\\
\phantom{..................}|\phantom{.....................}|\phantom{...........}|\phantom{.......................}|\phantom{..........}|\phantom{.....................}\\
\phantom{}\ce{2CH3 - C = O ->[Ba(OH)2] CH3 - C - CH2 - C = O ->[Δ/-H2O]\ce{CH3 - C = CH - C = O + H2O}}\\
\phantom{.............................}|\phantom{.................................}\ce{\underset{(B)}{4-Methypent-3-en-2-one}}\phantom{}\\
\ce{\underset{\underset{(A)}{4-Hydroxy-4-methyl pentan-2-one}}{OH}}\phantom{........................}
\end{array}\]
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संबंधित प्रश्न
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 :
What is meant by the following term? Give an example of the reaction in the following case.
Aldol
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.
- Methanal
- 2-Methylpentanal
- Benzaldehyde
- Benzophenone
- Cyclohexanone
- 1-Phenylpropanone
- Phenylacetaldehyde
- Butan-1-ol
- 2, 2-Dimethylbutanal
Write structural formulas and names of four possible aldol condensation products from propanal and butanal. In each case, indicate which aldehyde acts as nucleophile and which as electrophile.
How will you bring about the following conversion in not more than two steps?
Ethanol to 3-Hydroxybutanal
How will you bring about the following conversion in not more than two steps?
Benzaldehyde to 3-Phenylpropan-1-ol
Why is alpha (α) hydrogen of carbonyl compounds acidic in nature?
What is substituted imine called?
Cannizaro’s reaction is not given by ______.
Which product is formed when the compound 
is treated with concentrated aqueous \[\ce{KOH}\] solution?
Which of the following compounds do not undergo aldol condensation?
(i) \[\ce{CH3 - CHO}\]
(ii) 
(iii) \[\begin{array}{cc}
\phantom{}\ce{O}\\
\phantom{}||\\
\ce{CH3 - C - CH3}
\end{array}\]
(iv) \[\begin{array}{cc}
\phantom{}\ce{CH3}\\
|\phantom{...}\\
\ce{CH3 - C - CHO}\phantom{..}\\
|\phantom{...}\\
\phantom{}\ce{CH3}\\
\end{array}\]
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.
When liquid ‘A’ is treated with a freshly prepared ammoniacal silver nitrate solution, it gives bright silver mirror. The liquid forms a white crystalline solid on treatment with sodium hydrogensulphite. Liquid ‘B’ also forms a white crystalline solid with sodium hydrogensulphite but it does not give test with ammoniacal silver nitrate. Which of the two liquids is aldehyde? Write the chemical equations of these reactions also.
Convert the following:
Acetaldehyde to But-2-enal
Predict the reagent for carrying out the following transformations:
Ethanal to 3-hydroxy butanal
Explain the aldol condensation of ethanal.
Which of the following does not give aldol condensation reaction?
Which of the following compounds will undergo self-condensation in the presence of dilute NaOH solution?
Why is the α-hydrogens of aldehydes and ketones are acidic in nature?
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.
Write a note on the aldol condensation reaction of acetaldehyde.
What is aldol condensation? Explain it with suitable examples.
