The Kolbe-Schmitt reaction involves the reaction of a phenoxide ion with carbon dioxide to form salicylic acid, a key step often confused with Kolbe’s electrolysis in some curricula. In this context, we identify the electrophile used.
Step 1: Understand Kolbe’s reaction
Kolbe’s electrolysis produces alkanes from carboxylate salts, but the Kolbe-Schmitt reaction is relevant here, where sodium phenoxide reacts with \({CO_2}\) under heat and pressure to form salicylic acid. The electrophilic carbon in \({CO_2}\) is attacked by the nucleophilic phenoxide ion.
Step 2: Identify the electrophile
- (A) Carbondioxide: \({CO_2}\) has an electron-deficient carbon, acting as an electrophile in the Kolbe-Schmitt reaction, correct.
- (B) Dichlorocarbene: Used in Reimer-Tiemann reaction, not Kolbe’s.
- (C) Carbommonoxide: Not involved in Kolbe’s reactions.
- (D) Acyl carbocation: Relevant to Friedel-Crafts acylation, not Kolbe’s.
Step 3: Conclusion
The electrophile in the Kolbe-Schmitt reaction is carbon dioxide, matching option (A).