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Although phenoxide ion has more number o...

Although phenoxide ion has more number of resonating structures than carboxylate ion, carboxylic acid is a stronger than phenol. Why ?

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To understand why carboxylic acids are stronger acids than phenols, despite the phenoxide ion having more resonating structures than the carboxylate ion, we need to analyze the stability of their conjugate bases. ### Step 1: Define the Conjugate Bases - **Phenol** (C6H5OH) can lose a proton (H+) to form the **phenoxide ion** (C6H5O−). - **Carboxylic acid** (RCOOH) can lose a proton to form the **carboxylate ion** (RCOO−). ### Step 2: Analyze Resonance Structures - The **phenoxide ion** has several resonance structures where the negative charge can be delocalized over the carbon atoms of the aromatic ring. However, the negative charge remains primarily on the carbon atom. ...
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NCERT ENGLISH-ALDEHYDES, KETONES AND CARBOXYLIC ACIDS-Exercise
  1. What is meant by the following terms ? Give an example of the reaction...

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  2. Name the following compounds according to the IUPAC system of nomencla...

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  3. Draw the structures of following compound: i. 3-Methylbutanal ii. ...

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  4. Write the IUPAC names of following ketones and aldehydes. Wherever pos...

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  5. Draw the structure of following derivatives: i. 2,4-Dinitrophylhydra...

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  6. Predict the products formed when cyclohexane carbaldehyde reacts with ...

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  7. Which of the following compounds would undergo aldol condensation or t...

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  8. How will you convert ethnal into the following compounds ? i. Butane...

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  9. Write structure formulae and names of four possible aldol condensation...

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  10. Anorganic compound with molecular formula C9H10O forms 2,4-DNP deriva...

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  11. An organic compound (A) (molecular formula C(8)H(16)O(2)) was hydrolys...

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  12. Arrange the following compounds in increasing order of their property ...

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  13. Give simple chemical test to distinguish between the following pairs o...

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  14. How will you prapare the following compounds from benzene ? You may us...

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  15. How will you bring about the following conversions in not more than tw...

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  16. Describe the following i. Acetylation ii. Cannizzaro reaction i...

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  17. Complete each synthesis by giving missing starting material, reagent o...

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  18. Giving plausible explanation for each of the following: i. Cyclohexa...

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  19. An organic compound contains 69.77% carbon, 11.63% hydrogen, and rest ...

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  20. Although phenoxide ion has more number of resonating structures than c...

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