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Preparation: Rosenmund, Stephen, ozonolysis

Aldehydes and Ketones · Chemistry

Study notes

Prepare benzaldehyde from toluene without over-oxidation to benzoic acid. Step 1: Strong oxidation (KMnO₄) would give benzoic acid — too far! Step 2: Etard reaction: toluene + CrO₂Cl₂ (chromyl chloride) → chromium complex. Step 3: Hydrolysis → benzaldehyde (stops at aldehyde). Step 4: Controlled oxidation hits the aldehyde stage — Etard's precision!

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