ОН О OH ОН О H. B For the "crossed" aldol reaction that lead to product C, did the kind of base used make any difference to the reaction outcome? If so, what happened?
ОН О OH ОН О H. B For the "crossed" aldol reaction that lead to product C, did the kind of base used make any difference to the reaction outcome? If so, what happened?
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter26: Aldol And Claisen Reactions
Section: Chapter Questions
Problem 51CTQ
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Step 1
The structure of product C is represented as follows:
Step 2
The reaction in which two same or different carbonyl compounds containing alpha hydrogen are used with a base leads to removal of acidic hydrogen and forms an enolate ion which acts as a nucleophile for other carbonyl compound which is acting as an electrophile is termed as cross aldol reaction. If same carbonyl groups are used then there will be formation of 2 products but if different carbonyl groups are used then there will be formation of four different products.
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