How does the physical distance of an electron-withdrawing substituent (like ) along the carbon chain — GOC and Organic Chemistry Basics Chemistry Question
Question
How does the physical distance of an electron-withdrawing substituent (like $-Cl$) along the carbon chain affect the acidity of a carboxylic acid?
Answer: C
💡 Solution & Explanation
The inductive effect is a permanent polarization of $\sigma$ -bonds that decreases rapidly with distance. Therefore, moving the highly electronegative chlorine atom closer to the carboxyl group drastically increases its $-I$ pull, stabilizing the resulting carboxylate anion more effectively and increasing acidity.
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