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Consider following acid underset(I)(Cl...

Consider following acid
`underset(I)(ClCH_(2)COOH)," "underset(II)(CH_(3)COOH)," "underset(III)(CH_(3)CH_(2)COOH)`
Correct order of their pH value

A

`III lt II lt I`

B

`I lt II lt III`

C

`I lt III lt II`

D

`II lt I lt III`

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The correct Answer is:
To determine the correct order of pH values for the given acids, we need to analyze their acidic strengths based on their conjugate bases. The acids in question are: 1. ClCH₂COOH (I) 2. CH₃COOH (II) 3. CH₃CH₂COOH (III) ### Step 1: Identify the Conjugate Bases The first step is to identify the conjugate bases of each acid: - For ClCH₂COOH, the conjugate base is ClCH₂COO⁻. - For CH₃COOH, the conjugate base is CH₃COO⁻. - For CH₃CH₂COOH, the conjugate base is CH₃CH₂COO⁻. ### Step 2: Analyze the Stability of Conjugate Bases Next, we analyze the stability of these conjugate bases, as the stability is directly related to the strength of the corresponding acid: 1. **ClCH₂COO⁻**: The presence of the electronegative chlorine atom exerts a strong -I (inductive) effect, pulling electron density away from the carboxylate group. This stabilizes the negative charge on the conjugate base, making it a strong acid. 2. **CH₃COO⁻**: The methyl group (CH₃) has a +I (inductive) effect, which increases electron density on the carboxylate group, making the conjugate base less stable compared to ClCH₂COO⁻. Thus, CH₃COOH is a weaker acid than ClCH₂COOH. 3. **CH₃CH₂COO⁻**: The ethyl group (CH₃CH₂) also has a +I effect, which is even stronger than that of the methyl group. This leads to a further increase in electron density on the carboxylate group, making the conjugate base less stable than CH₃COO⁻. Therefore, CH₃CH₂COOH is the weakest acid among the three. ### Step 3: Determine the Order of Acidity From the analysis, we can summarize the strength of the acids: - ClCH₂COOH (I) is the strongest acid, resulting in the lowest pH. - CH₃COOH (II) is a weaker acid than ClCH₂COOH, resulting in a higher pH. - CH₃CH₂COOH (III) is the weakest acid, resulting in the highest pH. ### Conclusion: Order of pH Values Thus, the correct order of their pH values from lowest to highest is: **ClCH₂COOH (I) < CH₃COOH (II) < CH₃CH₂COOH (III)**
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MOTION-GOC-Exercise - 1
  1. Consider the following carbanions (i) CH(3)- overset(Ө)CH(2)" "(ii...

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  2. In which of the following compounds is hydroxylic proton the most acid...

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  3. Consider following acid underset(I)(ClCH(2)COOH)," "underset(II)(C...

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  4. Which of the following acids has lowest pK(a) value?

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  5. Arrange in decreasing pK(a) (a) F - CH(2) CH(2) COOH (b)Cl - under...

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  6. The correct order of increasing acid strength of the compounds (a) C...

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  7. Correct order of basic strength in gas phase is (I) CH(3)-NH(2) (II...

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  8. Arrange basicity of the given compounds in decreasing order - (a)CH(...

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  9. Which one of the following is the strongest base in aqueous solution?

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  10. In which of the following molecules, all atoms are not coplanar ?

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  11. (I) CH(2) = CH - CH = CH(2) (II) overset(Theta)CH(2) - CH = CH - ove...

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  12. Among these canonical structures, the correct order of stability is

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  13. Amongt these canonical structures which one is least stable ?

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  14. For phenol which ofthe following resonating structure is the most stab...

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  15. The most stable resonating structure of following compound is

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  16. Among these canonical structures of pyridiine, the correct order of st...

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  17. Write the stability order of Resonating Structures:

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  18. ‘M’ effect is the resonance of

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  19. Which of the following contain + M but -I effect -

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  20. In phenol , pi-electron-density is maximum on

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