The
Etard reaction is an important organic reaction that selectively oxidizes aromatic
methyl groups (
−CH3) into
aldehydes (
−CHO) using a specific oxidizing agent.
Step 1: Key Reagent in the Etard Reaction.
The key reagent used in the
Etard reaction is
chromyl chloride (
CrO2Cl2). This compound is a strong oxidizing agent that is used to convert
methyl groups on aromatic compounds, such as toluene, into
formyl groups (
−CHO) to form
benzaldehyde.
Step 2: Example Reaction.
For instance, when
toluene (
C6H5CH3) reacts with
chromyl chloride in a solvent like
carbon tetrachloride (
CCl4), the methyl group of toluene is oxidized to form
benzaldehyde (
C6H5CHO):
C6H5CH3+CrO2Cl2→C6H5CHO.
This is a typical example of how the Etard reaction works.
Conclusion:
The correct reagent used in the Etard reaction is
chromyl chloride (A).