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Which of the following carbonyl oxygen w...

Which of the following carbonyl oxygen will form strongest hydrogen bond with `H_(2)O` molecule?

A

B

C

D

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To determine which carbonyl oxygen will form the strongest hydrogen bond with an H₂O molecule, we need to analyze the stability of the negative charge on the oxygen atom in each given compound. Here’s a step-by-step breakdown of the solution: ### Step 1: Understand the Concept of Hydrogen Bonding Hydrogen bonding occurs when a hydrogen atom covalently bonded to a highly electronegative atom (like oxygen) interacts with another electronegative atom. In this case, we are looking at the interaction between the carbonyl oxygen and the hydrogen atoms of water (H₂O). ### Step 2: Analyze Each Compound We have four options (let's denote them as A, B, C, and D). We will analyze the stability of the negative charge on the carbonyl oxygen for each compound. #### Option A: - When the carbonyl bond breaks, the oxygen will carry a negative charge. - The structure is cyclic and planar but is anti-aromatic due to having 4 pi electrons. - Anti-aromatic compounds are unstable, which means the negative charge on oxygen is not stabilized. - **Conclusion**: This will not form the strongest hydrogen bond with water. #### Option B: - When the carbonyl bond breaks, the oxygen will carry a negative charge. - The structure is cyclic, planar, and has 6 pi electrons, which means it is aromatic. - Aromatic compounds are stable, so the negative charge on oxygen is stabilized. - **Conclusion**: This will form the strongest hydrogen bond with water. #### Option C: - When the carbonyl bond breaks, the oxygen will carry a negative charge. - The structure forms a 3-membered ring, which introduces angle strain and instability. - The positive charge is also not stabilized. - **Conclusion**: This will not form a strong hydrogen bond with water. #### Option D: - When the carbonyl bond breaks, the oxygen will carry a negative charge. - The structure is non-planar and non-aromatic due to sp³ hybridization. - Non-aromatic compounds are less stable than aromatic ones. - **Conclusion**: This will not form a strong hydrogen bond with water. ### Step 3: Final Conclusion After analyzing all options, we find that **Option B** has the most stable negative charge on the carbonyl oxygen, allowing it to form the strongest hydrogen bond with H₂O. ### Answer: **Option B** is the correct answer; it forms the strongest hydrogen bond with water. ---
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AAKASH INSTITUTE ENGLISH-ALDEHYDES, KETONES AND CARBOXYLIC ACIDS -Assignment (SECTION -B OBJECTIVE TYPES QUESTIONS (ONE OPTION IS CORRECT)
  1. Consider the following sequence of reactions: The final product [...

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  2. Consider the following sequence of reaction The final product [B]...

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  3. CH(3)-overset(O)overset(||)C-CH(3)overset("Conc")underset(HNO(3))to Pr...

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  5. The appropriate reagent for the transformation :

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  7. The product predominates is

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  8. Which of the following carbonyl oxygen will form strongest hydrogen bo...

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  9. Which of the following would be the best synthesis of benzoic acid fro...

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  10. Consider the following sequence of reactions: Major product [B] o...

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  11. The compound which is not reduced by LiAIH(4) is

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  12. Consider the following sequence of reactions. The product [A] and...

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  13. The compound can be compounded oxidized into

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  14. Which of the following conversion is known as Stefen's reduction?

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  15. Which reagent or sequence of reagents would best accomplish the follow...

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  16. An organic compound [X]. C(5)H(8)O reacts with hydroxylamine to form [...

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  17. Alanine can be obtained from acetaldehyde by the following sequence of...

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  18. Which of the following carboxylic acid ismost reluctant to form ester ...

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  19. Among the given compounds

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  20. A is

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