What are the products of oxidation of 2-methylcyclohexa-1,3-diene using hot concentrated acidified $\ce{KMnO4}$ solution?

Do we approach this problem the same way we would approach oxidation of alkenes?

I'm unsure how this mechanism would work.

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    $\begingroup$ Yes, pretty much. After all, you have two alkenes in your starting material. $\endgroup$ – orthocresol Mar 27 '17 at 0:03
  • $\begingroup$ Thank you for your answer. Could you draw out the products of oxidation of 2-methyl 1,3 cyclohexene? I'm unsure of how to start with this question. $\endgroup$ – Jonathan Smith Mar 29 '17 at 7:53

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