The conjugate base of diethyl malonate can serve as a nucleophile to attack a wide range of electrophiles. Identify the product that is formed when the conjugate base of diethyl malonate reacts with the following electrophile followed by acid workup when relevant: Modify the provided structures of diethyl malonate and the given electrophile to draw the product formed. Note: the eraser tool can be used to erase bonds, and atoms can be moved by selecting them with the selector tool and then dragging the selected atom(s) to a new position. If you make a mistake, you can use Ctrl-Z or the Undo tool. u EtO u O H₂C OEt CH3

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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The conjugate base of diethyl malonate can serve as a nucleophile to attack a wide range of electrophiles. Identify the product that is
formed when the conjugate base of diethyl malonate reacts with the following electrophile followed by acid workup when relevant:
ii
Incorrect.
Modify the provided structures of diethyl malonate and the given electrophile to draw the product formed. Note: the eraser tool can
be used to erase bonds, and atoms can be moved by selecting them with the selector tool and then dragging the selected atom(s) to a
new position. If you make a mistake, you can use Ctrl-Z or the Undo tool.
EtO
H₂C
O=
OEt
CH3
Transcribed Image Text:The conjugate base of diethyl malonate can serve as a nucleophile to attack a wide range of electrophiles. Identify the product that is formed when the conjugate base of diethyl malonate reacts with the following electrophile followed by acid workup when relevant: ii Incorrect. Modify the provided structures of diethyl malonate and the given electrophile to draw the product formed. Note: the eraser tool can be used to erase bonds, and atoms can be moved by selecting them with the selector tool and then dragging the selected atom(s) to a new position. If you make a mistake, you can use Ctrl-Z or the Undo tool. EtO H₂C O= OEt CH3
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