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Synthesis of Amino Acids: N-Phthalimidomalonic Ester Synthesis
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Synthesis of Amino Acids: N-Phthalimidomalonic Ester Synthesis
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29. Amino Acids / Synthesis of Amino Acids: N-Phthalimidomalonic Ester Synthesis / Problem 3
Problem 3
Which of the following describes the alkylation mechanism of an enolate anion through an SN2 process?
A
The enolate anion forms a double bond with the alkyl halide, releasing hydrogen gas.
B
The enolate anion rearranges to form a more stable carbocation before alkylation.
C
The enolate anion attacks the electrophilic carbon of an alkyl halide, displacing the halide ion.
D
The enolate anion is protonated by the alkyl halide, forming an alcohol.
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