CH3HCH₂CH₂CCH3CH3CHCH₂CH₂C-OCH₂CH₂CHCH3NaOH, H₂Oa. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown.• You do not have to consider stereochemistry.• Do not include counter-ions, e.g., Na+, I´, in your answer.• In cases where there is more than one answer, just draw one. b. Draw the structures of the organic products of the acyl transfer reaction.• You do not have to consider stereochemistry.• Draw the neutral form of the products; no charges.• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Separate multiple products using the + sign from the drop-down menu.?✪O. Sn [F

Ester shows an nucleophilic addition reaction because it has ester carbonyl group.

CH3 CH3 -OCH₂CH₂CHCH² NaOH, H₂O CH³CHCH₂CH₂C_OCH₂CH₂CHCH3 a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one.

CH3 CH3 -OCH₂CH₂CHCH² NaOH, H₂O CH³CHCH₂CH₂C_OCH₂CH₂CHCH3 a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section19.9: Crossed Enolate Reactions Using Lda

Problem JQ

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