The major product(s) obtained in the followin | vedclass

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(C) Step $1$: The reaction of $3$-bromocyclohexene with $KO^tBu$ (a strong,bulky base) undergoes an $E2$ elimination reaction to form $1,3$-cyclohexad

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(C) Step $1$: The reaction of $3$-bromocyclohexene with $KO^tBu$ (a strong,bulky base) undergoes an $E2$ elimination reaction to form $1,3$-cyclohexadiene.Step $2$: The subsequent reaction with $O_3/Me_2S$ is a reductive ozonolysis of $1,3$-cyclohexadiene.Step $3$: Reductive ozonolysis of $1,3$-cyclohexadiene cleaves both double bonds to yield two molecules of glyoxal $(OHC-CHO)$ and one molecule of succinaldehyde $(OHC-CH_2-CH_2-CHO)$.However,based on the provided options,the product is a mixture of $OHC-CH_2-CH_2-CHO$ and $OHC-CHO$.

The major product$(s)$ obtained in the following reaction is/are:

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