Exhibit 23-10
Consider the reaction below to answer the following question(s).
The Stork enamine reaction is a variation on the Michael reaction which utilizes an enamine nucleophile. 
-Refer to Exhibit 23-10.On the structures above,draw arrows indicating electron flow in each step of this reaction.
Correct Answer:
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Q11: In the alkylation of cyclohexanone,better yields are
Q12: Exhibit 23-10
Consider the reaction below to answer
Q13: Oxaloacetic acid is an important intermediate in
Q14: Exhibit 23-7
Consider the reaction below to answer
Q15: Give the structures of the ester precursors
Q17: Exhibit 23-5
Consider the reaction below to answer
Q18: Exhibit 23-8
Consider the compound 2-methyl-2-carboethoxycyclopentanone,whose structure is
Q19: Exhibit 23-8
Consider the compound 2-methyl-2-carboethoxycyclopentanone,whose structure is
Q20: Exhibit 23-3
Consider the data below to answer
Q21: Draw the general mechanism of a carbonyl
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