An ester A with molecular formula C9H10O2 was treated with excess of CH3MgBr and the complex so formed was treated with H2SO4 to give an olefin B . Ozonolysis of B gave a ketone with molecular formula C8H8O which shows positive iodoform test. The structure of A isAn
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C6H5COOC2H5
Explanation:
first ester in grignard reagent will form tertitary alcohol .
That alcohol on H2SO4 undergoes dehydration to give alkene .
alkene on O3/ozonolysis gave ketone (acc. to question)
the compond on ozonolysis should have methyl keto to give idoform test.
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