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.
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
What is meant by the following term? Give an example of the reaction in the following case.
Aldol
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
Describe the following:
Cross aldol condensation
Complete the synthesis by giving missing starting material, reagent or product.
\[\begin{array}{cc}
\ce{C6H5CHO}\phantom{............}\\
\phantom{........}\ce{+\phantom{......}\ce{->[dil.NaOH][\Delta]}}\phantom{...}\\
\ce{CH3CH2CHO}\phantom{............}
\end{array}\]
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.
Cross aldol condensation occurs between
The major product of the following reaction is:
Explain Aldol condensation of ethanal.