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Which of the following is strongest acid...

Which of the following is strongest acid among following

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To determine which of the given compounds is the strongest acid, we need to analyze the effects of the substituents on the carboxylic acid. The strength of an acid is often related to the stability of its conjugate base after the acid donates a proton (H⁺). Here’s a step-by-step breakdown of the solution: ### Step 1: Identify the Compounds We have four compounds with different substituents in the para position of a carboxylic acid: 1. Carboxylic acid with -OH (hydroxyl group) 2. Carboxylic acid with -NO2 (nitro group) 3. Carboxylic acid with -SO3H (sulfonic acid group) 4. Carboxylic acid with -CH3 (methyl group) ### Step 2: Understand Acid Strength The strength of an acid is determined by the stability of its conjugate base after it loses a proton (H⁺). A more stable conjugate base corresponds to a stronger acid. ### Step 3: Analyze the Substituents - **-NO2 (Nitro group)**: This is a strong electron-withdrawing group. It stabilizes the negative charge on the conjugate base through resonance and inductive effects. - **-SO3H (Sulfonic acid group)**: This is also a strong electron-withdrawing group, but not as strong as -NO2. - **-OH (Hydroxyl group)**: This group is weakly electron-withdrawing through resonance but can also donate electrons, making it less effective in stabilizing the conjugate base. - **-CH3 (Methyl group)**: This is an electron-donating group, which destabilizes the conjugate base by increasing electron density. ### Step 4: Compare the Effects Based on the electron-withdrawing strength: 1. -NO2 is the strongest electron-withdrawing group, thus stabilizing the conjugate base the most. 2. -SO3H follows as a strong electron-withdrawing group. 3. -OH is weaker in comparison. 4. -CH3 is an electron-donating group, which destabilizes the conjugate base. ### Step 5: Conclusion Since -NO2 provides the greatest stabilization to the conjugate base, the carboxylic acid with the -NO2 substituent is the strongest acid among the given options. ### Final Answer The strongest acid among the given options is the carboxylic acid with the -NO2 (nitro group) in the para position. ---
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ALLEN-CHEMISTRY AT A GLANCE-ORGANIC CHEMISTRY
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  2. (oversetE^(+))to major product major product will be

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  3. Which of the following is strongest acid among following

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  4. . Which of the following is not an electrophile?

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  5. The most unlikely resonating structures of pnitrophenoxide ion is :

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  6. Which of the following carbanion is most stable ?

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  7. Polarisation of sigma - bond is caused by polarisation of adjacent sig...

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  8. Select the molecule with more polar bond from each of the indicated bo...

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  9. Which of the following does not represent a correct set of nucleophile...

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  10. Which of the following is correct regarding formation of reactive inte...

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  11. In nitromethane two N-O bond lengths are :

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  12. Correct order of stability of the following resonating structure is ...

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  13. Which of the following have +M effect (overline e - donating mesomer...

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  14. Which of the following compounds does not show electromeric effect

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  15. Which of the following is not an example of +E effect:

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  16. Cyclooctatetraene is not aromatic . The most important reason for this...

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  17. Phenyl magnesium bromide reacts with methanol to give

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  18. Identify the end product in the given reaction sequence

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  19. The compound formed as a result of oxidation of ethyl benzene by KMnO(...

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