Hydrocarbon X has the formula C6H12. X reacts with one molar equivalent of hydrogen in the presence of a palladium catalyst to form a product having 12 primary hydrogens. Treatment of X with ozone followed by zinc in aqueous acid gives a mixture two aldehydes. What is the structure of X?

Hydrocarbon X has the formula C6H12. X reacts with one molar equivalent of hydrogen in the presence of a palladium catalyst to form a product having 12 primary hydrogens. Treatment of X with ozone followed by zinc in aqueous acid gives a mixture two aldehydes. What is the structure of X?

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter6: Reactions Of Alkenes

Section: Chapter Questions

Problem 6.31P: When 2-pentene is treated with Cl2 in methanol, three products are formed. Account for the formation...

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Question

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Hydrocarbon X has the formula C₆H₁₂.
X reacts with one molar equivalent of hydrogen in the presence of a palladium catalyst to form a product having 12 primary hydrogens.
Treatment of X with ozone followed by zinc in aqueous acid gives a mixture two aldehydes.
What is the structure of X?

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

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