Enamines can serve as enolate surrogates in reactions at the a-carbon. In the reaction sequence, the structures of the enamine addition product - the initial zwitterion and its neutral tautomer - are shown. Draw the structures of the two reactants forming these intermediates, and draw the structure of the final product, obtained via hydrolysis of the neutral intermediate. initial zwitterionic intermediate Reactants 'N'+ tautomerization hydrolysis product neutral intermediate + H₂O
Enamines can serve as enolate surrogates in reactions at the a-carbon. In the reaction sequence, the structures of the enamine addition product - the initial zwitterion and its neutral tautomer - are shown. Draw the structures of the two reactants forming these intermediates, and draw the structure of the final product, obtained via hydrolysis of the neutral intermediate. initial zwitterionic intermediate Reactants 'N'+ tautomerization hydrolysis product neutral intermediate + H₂O
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Draw the two reactants.
Draw the hydrolysis product.
O
Transcribed Image Text:Enamines can serve as enolate surrogates in reactions at the α-carbon. In the reaction sequence, the structures of the enamine
addition product - the initial zwitterion and its neutral tautomer - are shown. Draw the structures of the two reactants forming
these intermediates, and draw the structure of the final product, obtained via hydrolysis of the neutral intermediate.
initial zwitterionic intermediate
'N +
85
Reactants
tautomerization
hydrolysis
product
neutral intermediate
80
+
H₂O
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