Acetyl acetone in enol form have intramolecular H-bonding, which is absent in acetone.
enol form of Acetyl acetone is stabilised by conjugation and by intramolecular H-bonding.

enol form of acetone is very less (<0.1

JEE Main 2021 — Chemistry Organic Chemistry
Assertion A : Enol form of acetone [CH3COCH3] exists in <0.1 quantity. However, the enol form of acetyl acetone [CH3COCH2OCCH3] exists in approximately 15quantity.
Reason R : enol form of acetyl acetone is stabilized by intramolecular hydrogen bonding, which is not possible in enol form of acetone.
Choose the correct statement:
Held on 16 Mar 2021 · Verified 6 Jul 2026.
A is false but R is true
Both A and R are true and R is the correct explanation of A
Both A and R are true but R is not the correct explanation of A
A is true but R is false
Sign in to track your attempts and accuracy.
Sign in to keep a private note on this question. Nothing you write is ever public.
Sucrose hydrolyses in acidic medium into glucose and fructose by first order rate law with $t_{1/2} = 3$ hour. The percentage of sucrose remaining after $6$ hours is _______. (Nearest integer) (Given: $\log 2 = 0.3010$ and $\log 3 = 0.4771$)
Given below are two statements: Statement I: $\left(\mathrm{CH}_{3}\right)_{3} \stackrel{\oplus}{\mathrm{C}}$ is more stable than $\stackrel{\oplus}{\mathrm{C}} \mathrm{H}_{3}$ as nine hyperconjugation interactions are possible in $\left(\mathrm{CH}_{3}\right)_{3} \stackrel{\oplus}{\mathrm{C}}$. Statement II: $\stackrel{\oplus}{\mathrm{C}} \mathrm{H}_{3}$ is less stable than $\left(\mathrm{CH}_{3}\right)_{3} \stackrel{\oplus}{\mathrm{C}}$ as only three hyperconjugation interactions are possible in $\stackrel{\oplus}{\mathrm{C}} \mathrm{H}_{3}$. In the light of the above statements, choose the correct answer from the options given below
Given below are two statements: Statement I: Benzene is nitrated to give nitrobenzene, which on further treatment with $\mathrm{CH}_{3} \mathrm{COCl} / \mathrm{AlCl}_{3}$ will give  Statement II: $-\mathrm{NO}_{2}$ group is a $m$-directing, and deactivating group. In the light of the above statements, choose the most appropriate answer from the options given below
Arrange the following alkenes in decreasing order of stability.  Choose the correct answer from the options given below:
A hydroxy compound $(\mathrm{X})$ with molar mass $122 \mathrm{~g} \mathrm{~mol}^{-1}$ is acetylated with acetic anhydride, using a large excess of the reagent ensuring complete acetylation of all hydroxyl groups. The product obtained has a molar mass of $290 \mathrm{~g} \mathrm{~mol}^{-1}$. The number of hydroxyl groups present in compound (X) is:
Work through every JEE Main Organic Chemistry PYQ, year by year.