Alkenes on treating with $O_3$ and then the product on reduction may give

An alkene "A" on reaction with $O_3$ and Zn gives propanone and ethanol in equimolar Addition of HCl to alkene "A" gives "B" as the product. The structure of product "B" is:

An alkene A on reaction with $O_3$ and $Zn-H_{2}O$ gives propanone and ethanal in equimolar ratio. Addition of HCI to alkene A gives B as the major product. The structure of product B is

o-Methoxybromobenzene is treated with sodamide and then with ammonia. The product formed is

When $S{O}_3$ is treated with $D_{2}O$, the products are :

When $S{O}_3$ is treated with $D_{2}O$, the products are :

o-xylene on reductive ozonolysis gives

If an amide is treated with $P_2{O}_5$ the likely product is an

An alkene on ozonolysis gives only one product $\left(Z\right)$. $Z$ on reaction with Fehling solution give red precipitate of $C{u}_{2}O$. Alkene will be?

Alkenes can be oxidized in presence of different reagents to give different products. Alkenes on oxidation in presence of silver at high temperature give cyclic ethers, which also can be synthesized by using per acids. Alkenes on reductive ozonolysis give carbonyl compounds in presence of zinc and peroxide. On reaction with acidic KMnO4, it also produces corresponding carbonyl compound. Alkynes can also be oxidized in presence of such reagents but the products are different.
Cyclohexene is allowed to react with ozone and subsequently with $H_2{O}_2$ and water. The product formed is

Which of the following give the same product on the reduction with DIBAL-H?