Complete the following base-catalyzed Self-Aldol Condensation reaction mechanism. Draw the structure of the enolate anions, the aldol addition product, and the related intermediates. All lone pair electrons must be included in your drawing. No need to draw the curved arrows. Label the structures in your answer clearly as indicated in each box. 8 = :O-H EtOH Enolate anion Enolate anion s Final Product heat Alkoxide anion 1 H Aldol Addition Product Alkoxide anion 1 H O-Et Q-Et Aldol Addition Product Enolate anion :0-H /heat

Complete the following base-catalyzed Self-Aldol Condensation reaction mechanism. Draw the structure of the enolate anions, the aldol addition product, and the related intermediates. All lone pair electrons must be included in your drawing. No need to draw the curved arrows. Label the structures in your answer clearly as indicated in each box. 8 = :O-H EtOH Enolate anion Enolate anion s Final Product heat Alkoxide anion 1 H Aldol Addition Product Alkoxide anion 1 H O-Et Q-Et Aldol Addition Product Enolate anion :0-H /heat

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

See image below
See image below
Draw the product for the following reaction.This is what my homework assignment is asking for, the question is complete
The enolate of an ester can be treated with a ketone to give a beta-hydroxy ester. Draw a mechanism for this aldol-like reaction. For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph. EtO 1) LDA 2) ΕΙΟ OH श्र Step 1 * Incorrect. Which of the mechanistic steps is shown in this step of the mechanism? Draw step 1 of the mechanism. HC CH CH3 CH3 Edit Drawing CH3
See image below
5. Draw the mechanism of the aldol reaction between your aldehyde and ketone, and draw the final product after dehydration. 2:R- CH, Aldehyde Ketone 6. Make a table of predicted IR peaks for your aldehyde, ketone, and aldol product. You may give general ranges for the peaks on the IR spectra. Make 3 separate tables.
Draw the product of each of the following ring-closing reactions.
6. For the following reaction, draw all of the synthetic intermediates that are formed in each step, including the final product. 1. H2SO4 2. mCPBA 3. MgBr-CH2CH3 4. H20 HO.
Draw an alkyl bromide that would produce ONLY the following alkene in an E2 elimination. Ignore any inorganic byproducts.
Show structures (in blank boxes) for the reactants/products in the following reactions.
Select reactants and reagents that can be used in a crossed Aldol Condensation to make the following molecule Select reactants and reagents that can be used in a crossed Claisen Condensation to make the following molecule,
This question has multiple parts. Work all the parts to get the most points. The Stork reaction is a condensation reaction between an enamine donor and an a,ß-unsaturated carbonyl acceptor. The overall reaction consists of a three-step sequence of 1. formation of an enamine from a ketone, 2. Michael addition to an a,ß-unsaturated carbonyl compound, and 3. hydrolysis of the enamine in dilute acid to regenerate the ketone. Consider the Stork reaction between cyclohexanone and propenal. 1 Draw the structure of the product of the enamine formed between cyclohexanone and pyrrolidine. TAYY { n [F ? ChemDoodle Previous Next