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Find the strongest acid among the follow...

Find the strongest acid among the following compound

A

`HOOC-(CH_(2))_(2)-COOH`

B

`overset(+)NH_3-(CH_(2))_(2)-COOH`

C

`F-(CH_(2))_(2)-COOH`

D

`CH_(3)-(CH_(2))_(2)-COOH`

Text Solution

AI Generated Solution

The correct Answer is:
To determine the strongest acid among the given compounds, we need to analyze the structures of the compounds and their ability to donate protons (H⁺ ions). Here’s a step-by-step solution: ### Step 1: Identify the Functional Groups All the compounds mentioned in the question have a carboxylic acid group (COOH), which is responsible for their acidic nature. We need to compare their acidity based on the substituents attached to the carboxylic acid group. ### Step 2: Understand Acid Strength The strength of an acid is determined by how easily it can donate a proton (H⁺). The more stable the conjugate base formed after the donation of H⁺, the stronger the acid. ### Step 3: Evaluate Electron Withdrawing Groups Electron withdrawing groups (EWGs) stabilize the negative charge on the conjugate base, making it easier for the acid to donate a proton. The presence of strong EWGs increases the acidity of the compound. ### Step 4: Analyze Each Compound - **Compound A (COOH)**: This compound has no strong electron withdrawing groups. Therefore, it will have a moderate acidity. - **Compound B (NH3⁺ attached to COOH)**: The presence of the positively charged NH3⁺ group acts as a strong electron withdrawing group. This increases the positive charge density on the hydrogen of the carboxylic acid, making it easier to lose H⁺ and thus increasing its acidity. - **Compound C (Fluorine attached to COOH)**: Fluorine is an electron withdrawing group, but it is not as strong as the NH3⁺ group. While it does stabilize the conjugate base, it does not do so as effectively as the NH3⁺ group. ### Step 5: Compare Compounds B and C Between compounds B and C, the NH3⁺ group in compound B is a stronger electron withdrawing group than the fluorine in compound C. Therefore, compound B will be more acidic than compound C. ### Conclusion Based on the analysis, **Compound B (NH3⁺ attached to COOH)** is the strongest acid among the given compounds. ---

To determine the strongest acid among the given compounds, we need to analyze the structures of the compounds and their ability to donate protons (H⁺ ions). Here’s a step-by-step solution: ### Step 1: Identify the Functional Groups All the compounds mentioned in the question have a carboxylic acid group (COOH), which is responsible for their acidic nature. We need to compare their acidity based on the substituents attached to the carboxylic acid group. ### Step 2: Understand Acid Strength The strength of an acid is determined by how easily it can donate a proton (H⁺). The more stable the conjugate base formed after the donation of H⁺, the stronger the acid. ...
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A2Z-SOME BASIC PRINCIPALS OF ORGANIC CHEMISTRY-Section D - Chapter End Test
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  5. Which one of the following compounds is most acidic

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  8. The following reaction is described as

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  9. Which of the following is the most stable cation?

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  10. The observed dipole moment of nitromethane is highly than the dipole m...

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  11. Dehydrohalogenation in presence of OH^(-) is correct represented by

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  12. Among the following the aromatic compound is

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  13. Which of the following compounds are not arranged in order of decreasi...

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  14. Most stable carbonium ion is :

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  15. Which one of the following species is most stable

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  16. Which of the following gives most stable carbocation by dehydration

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  17. Which of the following free radicals would be expected to be most sele...

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  18. The +I effect of alkyl groups is in the order

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  19. How many carbon atoms in the molecule HCOO-(CHOH)(2)-COOH are asymmetr...

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  20. With a change in hybridisation of the carbon bearing the charge, the s...

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