Assertion : `alpha`-hydrogen atoms in aldehydes or ketones are acidic.
Reason : Anions formed aftrt the loss of `alpha`-hydrogen atoms are stablished due to inductive effect.

Give reason: prop - hydrogen atoms of aldehydes and ketones are acidic.

Assertion (A) The alpha -hydrogen atom in carbonyl compounds is less acidic. Reason (R) The anion formed after the loss of alpha -hydrogen atom is resonance stabilised.

Assertion (A) The alpha -hydrogen atom in carbonyl compounds is less acidic. Reason (R) The anion formed after the loss of alpha -hydrogen atom is resonance stabilised.

Why are alpha -hydrogen atom of aldehydes and ketones acidic in nature?

Why are alpha -hydrogen atom of aldehydes and ketones acidic in nature?

Why are alpha -hydrogen atom of aldehydes and ketones acidic in nature?

(A) alpha -Hydrogen atoms in aldehdes and ketones are acidic. (R) The anion left after the removal of alpha -hydrogen from carbonly compounds is stabilized by the electron withdrawing carbonyl group.

Why is Alpha - hydrogens of aldehyde or ketone very important.

This question contains two statements: Statement 1 and Statement 2. This question has four alternative choices, only one of which is the correct answer. Statement 1: The alpha -hydrogen atom in carbonyl compounds is basic. Statement 1: The anion formed after the loss of alpha -hydrogen atom from carbonyl compound is resonance stabilised.