Oxidation of toluene with dilute HNO_3 gives: | vedclass

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(C) The oxidation of toluene with dilute $HNO_3$ is not a standard method for producing benzaldehyde or benzoic acid. However,in the context of typica

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Nitrotoluene

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(C) The oxidation of toluene with dilute $HNO_3$ is not a standard method for producing benzaldehyde or benzoic acid. However,in the context of typical chemistry curriculum questions,if the reaction is intended to represent the oxidation of the methyl group,it usually requires strong oxidizing agents like $KMnO_4$ to form benzoic acid. If the question implies the reaction of toluene with $HNO_3$ (nitration),it would yield nitrotoluene. Given the options,the most chemically accurate reaction for toluene with $HNO_3$ is electrophilic aromatic substitution,which produces $o$-nitrotoluene and $p$-nitrotoluene.

Oxidation of toluene with dilute $HNO_3$ gives:

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