Final answer:
The product from reductive ozonolysis of 1,2-methylcyclohexane is 1,2-dimethylcyclohexane-1,2-diol, which has two alcohol groups where the double bond in the cyclohexene ring was cleaved.
Step-by-step explanation:
The structure for the product from reductive ozonolysis of 1,2-dimethylcyclohexene involves breaking the double bond and forming two carbonyl groups. The reductive part signifies that the oxygen-oxygen bond is also broken and the resulting fragments are 'reduced', meaning that any carbonyl groups formed during the reaction would be further reduced to alcohols. In the case of 1,2-dimethylcyclohexene, the ozonolysis cleaves the alkene to form two ketone fragments which are then reduced to alcohols, leading to the formation of 1,2-dimethylcyclohexane-1,2-diol.