A compound A (C6H) undergoes catalytic hydrogenation over Lindlar catalyst to give a compound B, which in
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A compound A (C6H) undergoes catalytic hydrogenation over Lindlar catalyst to give a compound B, which in turn undergoes ozonolysis followed by workup with aqueous H2O2 to yield succinic acid and two equivalents of formic acid. In the absence of a catalyst poison, hydrogenation of A gives hexane. Propose a structure for compound A.
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The ozonolysis results define compound B as 1 5hexadi...View the full answer
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