Which of the following has highly acidic hydrogen?
- A
Structure
- B
Structure
- C
Structure
- D
Structure
Which of the following has highly acidic hydrogen?
Structure
Structure
Structure
Structure
Correct answer:D
Standard Method
Given: The question asks which structure has a highly acidic hydrogen.
Find: The correct option containing the most acidic hydrogen.
From the solution, the correct option is D.
The key idea is to compare how stable the conjugate base becomes after removal of a proton. A hydrogen is highly acidic when its removal gives a strongly resonance-stabilized anion.
For structure , the methylene group lies between two carbonyl groups . On removal of a hydrogen, the resulting negative charge is delocalized over both carbonyl groups by resonance.
Because the conjugate base is much more stable, the hydrogen in structure is highly acidic.
Therefore, the correct option is D.
Why Structure 4 Is Most Acidic
Given: Acidic hydrogen depends on the stability of the conjugate base formed after deprotonation.
Find: Why structure has highly acidic hydrogen.
In structure , the hydrogen is present on a methylene carbon located between two carbonyl groups. After loss of , the carbanion formed is resonance stabilized.
The negative charge does not remain localized on one carbon atom. It is delocalized toward both adjacent carbonyl groups, which greatly stabilizes the conjugate base.
This is why hydrogen on an active methylene group between two groups is much more acidic than ordinary alkane hydrogens and more acidic than many other common functional group hydrogens.
Hence, structure contains the highly acidic hydrogen, so the correct option is D.
Students often identify acidity only by the presence of an group. This is incorrect because acidity depends on conjugate-base stabilization. Check whether deprotonation gives resonance stabilization, as in the active methylene group of structure .
A common mistake is to compare the hydrogen atom itself rather than the species formed after its removal. The correct approach is to compare the stability of the conjugate bases formed from each option.
Some students miss that a methylene group between two carbonyl groups is unusually acidic. This is wrong because the adjacent carbonyl groups delocalize the negative charge by resonance. Look for electron-withdrawing groups on both sides of the acidic carbon.
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