Ignoring stereochemistry,the 1:1 reaction of bromine with 1,3-cyclohexadiene at 25$\degree$C in the dark and in the absence of peroxide forms which of these?

Question

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The reaction of bromine with 1,3-cyclohexadiene in the absence of peroxide will result in the formation of both products I and II. This is a classic example of a Diels-Alder reaction, where the diene (1,3-cyclohexadiene) reacts with the dienophile (bromine) to form a cyclohexene ring. The reaction can proceed in two ways, resulting in either product I or product II. The stereochemistry of the reaction is not specified, so both products are possible.

Ignoring Stereochemistry,the 1:1 Reaction of Bromine with 1,3-Cyclohexadiene at 25 °\degree°

Ignoring Stereochemistry,the 1:1 Reaction of Bromine with 1,3-Cyclohexadiene at 25 $\degree$