Answered: Bicyclic ketone A rapidly equilibrates…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterNW4: Nomenclature Worksheet 4: Carbonyl Compounds

Section: Chapter Questions

Problem 1CTQ

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Bicyclic ketone A rapidly equilibrates with a stereoisomer upon treatment with strong base, but ketone B does not. Explain why in a post with others in your group. Comment on the posts of at least two other students - have they correctly explained the difference in behavior between ketones A and B?

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

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