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Which of the following is most acidic ?...

Which of the following is most acidic ?

A

B

C

D

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The correct Answer is:
To determine which of the given compounds is the most acidic, we need to analyze the stability of the conjugate base formed when each acid donates a proton (H+). The more stable the conjugate base, the stronger the acid. ### Step-by-Step Solution: 1. **Identify the Compounds**: Let's denote the compounds as A, B, C, and D. Assume they are different benzoic acids with varying substituents (e.g., nitro, methyl, etc.). 2. **Understand the Acid-Base Reaction**: When an acid (HA) donates a proton, it forms a conjugate base (A-). The acidity of HA can be assessed by the stability of A-. 3. **Draw the Conjugate Bases**: For each compound, draw the structure of the conjugate base after the proton is removed. This will help visualize the stabilization of the negative charge. 4. **Analyze the Stabilization Factors**: The stability of the conjugate base can be influenced by: - **Inductive Effect**: Electronegative groups (like -NO2) can stabilize the negative charge through the inductive effect. - **Resonance**: If the negative charge can be delocalized over multiple atoms, it increases stability. - **Hyperconjugation**: Alkyl groups can destabilize the negative charge due to electron-donating effects. 5. **Compare the Effects of Substituents**: - **Compound with -NO2 (Nitro Group)**: This group has a strong -M (minus mesomeric) effect, which stabilizes the negative charge on the conjugate base by delocalization. - **Compound with -CH3 (Methyl Group)**: This group has a +I (plus inductive) effect, which destabilizes the negative charge. - **Compound with no substituents**: This will have moderate stability. - **Compound with -OCH3 (Methoxy Group)**: This group has a +M effect, which can also destabilize the negative charge. 6. **Determine the Most Acidic Compound**: Based on the above analysis, the compound with the nitro group (-NO2) will be the most acidic because it effectively stabilizes the conjugate base through resonance and inductive effects. ### Conclusion: The most acidic compound among A, B, C, and D is the one with the nitro group, which is nitrobenzoic acid. ---
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MODERN PUBLICATION-ALDEHYDES ,KETONES AND CARBOXYLIC ACIDS-REVISION EXERCISES (OBJECTIVE QUESTIONS - MULTIPLE CHOICE QUESTIONS )
  1. Which on heating with aqueous KOH, produces acetaldehyde?

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  2. Iodoform test is not given by

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  3. In the following, strongest acid is :

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  4. in the following reaction , product P is

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  5. Acetaldehyde and acetone can be distinguished by

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  6. A carbonyl group can be converte into-CH(2) group by:

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  7. Among the following compounds, which will not repond to cannizzaro's r...

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  8. The IUPAC name of PhCH2 CH2 COOH is named as

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  9. Which of the following compound undergoes haloform reaction?

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  10. Which of the following is most acidic ?

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  11. Which of the following is the strongest acid:

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  12. What type of organic compounds are prepared by Gattermann-Koch reactio...

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  13. the IUPAC name of the compound is

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  14. In the reaction the product P is

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  15. Match the name reaction ( column I) with the reagent ( column II...

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  16. Match the name reaction ( column I) with the reagent ( column II...

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  17. Match the name reaction ( column I) with the reagent ( column II...

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  18. Match the name reaction ( column I) with the reagent ( column II...

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  19. Match the name reaction ( column I) with the reagent ( column II...

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  20. Match the name reaction ( column I) with the reagent ( column II...

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