Consider the following structures:
$I.$ $CH_3-CH_2-COOH$
$II.$ $CH_3-CH(Cl)-COOH$
$III.$ $Cl-CH_2-CH_2-COOH$
$IV.$ $CH_3-CH_2-CH_2-COOH$
The correct order of their acidity is

  • A
    $II > III > I > IV$
  • B
    $II > I > III > IV$
  • C
    $IV > III > II > I$
  • D
    None of these

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Similar Questions

Given below are two statements:
Statement $I$: On the basis of inductive effect, the order of stability of alkyl carbanions is $CH_3^- > CH_3CH_2^- > (CH_3)_2CH^- > (CH_3)_3C^-$.
Statement $II$: Allyl and benzyl carbanions are more stabilised by inductive effect and not by resonance effect.

In which type of molecule are the electrons of a $\pi$ bond delocalized?

Which of the following represents an incorrect electromeric effect?

Which of the following represents the hyperconjugation effect?

The most stable carbocation among the following is:

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