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CBSE Class 11-science Answered

A hydrocarbon 'X' takes up two molecules of hydrogen and is converted into a saturated hydrocarbon. On ozonolysis, 'X' gives a mixture of three carbonyl compounds namely, acetaldehyde, acetone and propan-1, 3-dial. Assign structure to compounds X.
Asked by Topperlearning User | 01 Jun, 2016, 02:00: PM
answered-by-expert Expert Answer

Since the compound takes up two molecules of hydrogen, it must have  two double bonds. The formation of three products on ozonolysis indicates that the compounds have unsaturation at two places. The equations are:

Answered by | 01 Jun, 2016, 04:00: PM

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