A hydrocarbon containing two double bonds on reductive ozonolysis gave glyoxal, ethanal and propanone . Give the structure of the hydrocarbon along with its IUPAC name .

A hydrocarbon containing two double bonds on reductive ozonolysis gave

1.	A hydrocarbon containing two double bonds on reductive ozonolysis gave glyoxal, ethanal and propanone . Give the structure of the hydrocarbon along with its IUPAC name .
Answer» Solution :To write the structure of the products of OZONOLYSIS with their carbonyl GROUPS facing each other. `underset"ETHANAL"(CH_3-oversetoverset(H)(\|)C=O) "" underset"Glyoxal"(O=oversetoverset(H)\|C-oversetoversetH\|C=O)"" underset"Propanone"(O=oversetoverset(CH_3)\|C-CH_3` Step 2 . To write the structure of the hydrocarbon Remove oxygen atoms from each of the three carbonyl COMPOUNDS and connect them by double bonds , we have, `underset"2-Methylhexa-2,4-diene"(underset6CH_3-underset5oversetoversetH\|C=underset4oversetoversetH\|C-underset3oversetoversetH\|C=underset2oversetoverset(CH_3)\|C-underset1CH_3)` Thus, the GIVEN hydrocarbon is 2-methylhexa-2,4-diene.