Products from Carbonyl-Containing Nucleophiles1) Draw the mechanism/intermediates and predict the products for the following ClaisenCondensation (note: I won't draw two copies of the reactant on homework or evaluations):i) NaOCH,CH,,CH,CH,OHii) H,O*the intermediates andthe products for the follovAcetoacetic Esteri) Naoii)Briii) acid and heat3) Draw the intermediates and predict the products for the following Malonic Ester Synthesis:i) NaOEtii)BrEtOOEtii) acid and heat4) For each of the above reactions, circle the parts of the reactants that are removed/lost duringthe reactions.

Answered: Image /qna-images/answer/15bcddef-cca6-4fcc-b14f-076a172a368c.jpg

1) Draw the mechanism/intermediates and predict the products for the following Claisen Condensation (note: I won't draw two copies of the reactant on homework or evaluations): i) NaOCH,CH,, CH,CH,OH ii) H,0* 2) Draw the intermediates and predict the products for the following Acetoacetic Ester Synthesis: i) Nao ii) Br iii) acid and heat 3) Draw the intermediates and predict the products for the following Malonic Ester Synthesis: i) NaOEt ii) Br iii) acid and heat EtO OEt

1) Draw the mechanism/intermediates and predict the products for the following Claisen Condensation (note: I won't draw two copies of the reactant on homework or evaluations): i) NaOCH,CH,, CH,CH,OH ii) H,0* 2) Draw the intermediates and predict the products for the following Acetoacetic Ester Synthesis: i) Nao ii) Br iii) acid and heat 3) Draw the intermediates and predict the products for the following Malonic Ester Synthesis: i) NaOEt ii) Br iii) acid and heat EtO OEt

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

Draw the mechanism for the following reaction. synthesis of 4-chlorobenzoic acid from 4-chlorobenzyl alcohol CH2OH اف C CI 4-Chlorobenzyl alcohol AcOH Ca(CIO)2 CI 4-Chlorobenzoic acid COOH
b) whee hi P from HOCH₂CH₂CH₂CH₂OH 3. Propose a mechanism for the following reaction: you H* + H₂O
Propose a synthesis for the following reaction
A set of three nucleophilic displacement reactions is shown below: - Br -Br -Br "CHз Hзс CHз C В A NaCN CH-он SN2 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?
Methamphetamine can exist in two possible forms, shown below: Mr. Mema is trying to convert structure A into structure B, but he forgot what Mr. Eme told him to do. Which of the reagents below can Mema add to A to get the desired B? * A B O H2 O NAOH HCI Nacl ェZエ

Which of the following is the best HBA? b) c) d) R-N lix XR R-C Oa) Ob) Od d) O= OH R-P
3.4) Propose a mechanism for the base-catalysed reaction below: H Н HO H Н -OH н -OH OH CH₂OH NaOH Но HO H H CH₂OH :0 -H -OH -OH CH₂OH
Select the major product of the following reaction: Me Me "H 1) LIAID 2) H₂O+ ?
How would I synthesize this reaction without losing the OH?
2) Rank the following carbonyl compounds in order of acidity (1 = most acidic, 4 = least acidic): O l i NMе₂ OEt Ph
17) Draw the product of the following reaction sequence: H2 1) SOCI, 2) CH;CH,CH,CH,NH, ОН 3) LİAIH4 4) H2O
R Please don't provide the handwriting solution