Chemistry, 08.04.2021 19:00 mooreadrian41235
Compound A (C9H12) absorbed 3 equivalents of H2 on catalytic reduction over a palladium catalyst to give hydrocarbon B (C9H18). Upon ozonolysis, compound A gave, among other things, a ketone that was identified as cyclohexanone. Upon treatment with an NaNH2 in liquid NH3 followed by addition of iodomethane, compound A gave a new hydrocarbon C (C10H14). What is the structure of starting Compound A
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Compound A (C9H12) absorbed 3 equivalents of H2 on catalytic reduction over a palladium catalyst to...
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