Chemistry, asked by surajekka4300, 1 year ago

An unknown alkene a on reductive ozonolysis gives two isomeric carboxyl compoind b and c having molecular formula c3h6o write the compoundss

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Answered by yogesh628
8

please mark as brainlist

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Answered by Tulsi4890
4

The compounds a, b, and c are 2-Methylpent-2-ene, Proapn-1-one, and Propan-2-one respectively.

  • Ozonolysis is an organic reaction in which the unsaturated bonds of an alkene or alkyne are cleaved in the presence of ozone.
  • The products are formed such that the multiple carbon-carbon bonds get replaced by a carbonyl group (C=O).
  • Hence the product formed is either an aldehyde ( - CH = O) or a ketone.
  • In the given question, the two compounds formed have the formula C₃H₆O. This means that the reactant (a) must have 6 carbons.
  • The complete reaction is shown below.
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