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Concept explainers
Interpretation:
A pair of compounds which is the most reasonable source of all the carbon atoms in the preparation of the given epoxide is to be determined.
Concept Introduction:
Dianion can be prepared from alpha halogenated carboxylic acids by double deprotonation using strong bases such as LDA.
Reaction of dianion of these alpha halogenated carboxylic acids with
In the first step, a new carbon-carbon single bond is formed between the carbonyl carbon of the ketone and the alpha carbon atom of the dianion.
In the second step, the oxygen atom in ketone attacks on the alpha carbon atom of the dianion to form a new carbon-oxygen single bond.
The oxygen atom in the ketone group is a source of oxygen in the
The original
In the process, a carbon-carbon single bond and a carbon-oxygen single bond are formed.
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Chapter 21 Solutions
ORGANIC CHEMISTRY-W/STUD.SOLN.MAN.
- Steps and explanation.arrow_forwardProvide steps and explanation please.arrow_forwardDraw a structural formula for the major product of the acid-base reaction shown. H 0 N + HCI (1 mole) CH3 N' (1 mole) CH3 You do not have to consider stereochemistry. ● • Do not include counter-ions, e.g., Na+, I, in your answer. . In those cases in which there are two reactants, draw only the product from 989 CH3 344 ? [Farrow_forward
- Assign these protonarrow_forwardCould you please solve the first problem in this way and present it similarly but color-coded or step by step so I can understand it better? Thank you!arrow_forwardCould you please solve the first problem in this way and present it similarly but color-coded or step by step so I can understand it better? Thank you!arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
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