Advertisements
Advertisements
Question
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.
Options
Assertion and reason both are correct and reason is correct explanation of assertion.
Assertion and reason both are wrong statements.
Assertion is correct statement but reason is wrong statement.
Assertion is wrong statement but reason is correct statement.
Assertion and reason both are correct statements but reasson is not correct explanation of assertion.
Advertisements
Solution
Assertion is wrong statement but reason is correct statement.
Explanation:
Because of the presence of electron-withdrawing carbonyl group, the alpha hydrogen atom in carbonyl compounds is acidic. In nature, hydrogen is very acidic.
Because the cation is released in the form of \[\ce{H-}\], the anion created after the loss of the -hydrogen atom is resonance stabilised.
APPEARS IN
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 :

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
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
Describe the following:
Cross aldol condensation
Give reasons Acetylation of aniline reduces its activation effect.
Why is alpha (α) hydrogen of carbonyl compounds acidic in nature?
Write chemical equations of the following reaction :
Benzoyl chloride is hydrogenated in the presence of `"Pd"/(BaSO_4)`
Explain aldol condensation reaction in detail.
Which product is formed when the compound
is treated with concentrated aqueous \[\ce{KOH}\] solution?
Which of the following conversions can be carried out by Clemmensen Reduction?
(i) Benzaldehyde into benzyl alcohol
(ii) Cyclohexanone into cyclohexane
(iii) Benzoyl chloride into benzaldehyde
(iv) Benzophenone into diphenyl methane
What product will be formed on reaction of propanal with 2-methylpropanal in the presence of \[\ce{NaOH}\]? What products will be formed? Write the name of the reaction also.
Cross aldol condensation occurs between
Which of the following gives aldol con~ensation reaction?
The major product of the following reaction is:

Which of the following does not give aldol condensation reaction?
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.
