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Rank these acids according to their expected pKa values.ClCH2COOHClCH2CH2COOHCH3CH2COOHCl2CHCOOHIn order of highest pka to lowest pka

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Answer: CH₃CH₂CH₂COOH > CH₃CH₂COOH > ClCH₂CH₂COOH > ClCH₂COOH

User Timothyqiu
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Answer:

CH₃CH₂CH₂COOH > CH₃CH₂COOH > ClCH₂CH₂COOH > ClCH₂COOH

Step-by-step explanation:

Electron-withdrawing groups (EWGs) increase acidity by inductive removal of electrons from the carboxyl group.

Electron-donating groups (EDGs) decrease acidity by inductive donation of electrons to the carboxyl group.

  • The closer the substituent is to the carboxyl group, the greater is its effect.
  • The more substituents, the greater the effect.
  • The effect tails off rapidly and is almost zero after about three C-C bonds.

CH₃CH₂-CH₂COOH — EDG — weakest — pKₐ = 4.82

CH₃-CH₂COOH — reference — pKₐ = 4.75

ClCH₂-CH₂COOH — EWG on β-carbon— stronger — pKₐ = 4.00

ClCH₂COOH — EWG on α-carbon — strongest — pKₐ = 2.87

User Emilee
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