Step 2. Draw the ester-containing intermediate produced from step 1, and draw the next reactant or reagent, if applicable. Add curved arrows and any necessary charges and nonbonding electrons. Select Draw Rings More Erase

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter14: Elimination
Section: Chapter Questions
Problem 22E
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Step 2. Draw the ester-containing intermediate produced from step 1, and draw the next reactant or reagent, if
applicable. Add curved arrows and any necessary charges and nonbonding electrons.
Select
Draw
Rings
More
Erase
Transcribed Image Text:Step 2. Draw the ester-containing intermediate produced from step 1, and draw the next reactant or reagent, if applicable. Add curved arrows and any necessary charges and nonbonding electrons. Select Draw Rings More Erase
2. H3O*
Show the curved-arrow mechanism for the Claisen condensation of ethyl ethanoate treated with ethoxide ion. Include all
formal charges and nonbonding electrons. In each step, draw only the species that react in that step. If an enolate
resonance form is possible, draw only the carbanionic form. If a CH, group is being deprotonated, draw all H's on the
reacting site. Tip: always omit ethanol byproducts.
Step 1. Add curved arrows.
Select
Draw
Rings
More
Erase
:0 :
H.
H
H
H
H
Transcribed Image Text:2. H3O* Show the curved-arrow mechanism for the Claisen condensation of ethyl ethanoate treated with ethoxide ion. Include all formal charges and nonbonding electrons. In each step, draw only the species that react in that step. If an enolate resonance form is possible, draw only the carbanionic form. If a CH, group is being deprotonated, draw all H's on the reacting site. Tip: always omit ethanol byproducts. Step 1. Add curved arrows. Select Draw Rings More Erase :0 : H. H H H H
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