1.

An unsaturated hydrocarbon on ozonolysis gives one mole each of methanal, ethanal and 2-ketopropanal. The structure of the hydrocarbon is

Answer»

`CH_2=CH-CH=CHCH_3`
`CH_3CH = CH-CH =CHCH_3`
`CH_2=C(CH_3)-CH=CHCH_3`
`CH_2=CH-C(CH_3)=CHCH_3`

Solution :ALKENES (c ) and (d) have same substitution in the TERMINAL double bonds but differ in the position of the `CH_3` group on the two internal CARBON atoms and hence give the same products on ozonolysis.


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