What is the reactive intermediate in the autooxidation of cyclohexene?

Question

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The autooxidation of cyclohexene involves the formation of an allylic radical as the reactive intermediate. This is because the double bond in cyclohexene undergoes cleavage to form a primary allylic radical, which then reacts with oxygen to form a peroxy radical. This peroxy radical can then go on to initiate a chain reaction that produces a range of different oxidation products.

What Is the Reactive Intermediate in the Autooxidation of Cyclohexene ∘\circ∘

What Is the Reactive Intermediate in the Autooxidation of Cyclohexene $\circ$