The following is an aldol condensation reaction, involving two different carbonyl compounds, one with a-protons and the other without any a-proton. only H,C CH3 (1) (2) (Product) Write the detailed mechanisms to show how you arrive at the final product. . (ii) Some side reactions may occur in the above aldol condensation reaction. Write one side reaction that you think it may happen. Detail mechanisms are not required.

The following is an aldol condensation reaction, involving two different carbonyl compounds, one with a-protons and the other without any a-proton. only H,C CH3 (1) (2) (Product) Write the detailed mechanisms to show how you arrive at the final product. . (ii) Some side reactions may occur in the above aldol condensation reaction. Write one side reaction that you think it may happen. Detail mechanisms are not required.

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

Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions

Section: Chapter Questions

Problem 20.54P

See similar textbooks

Similar questions

Write the products for (A-I). Label products with the mechanism (Sn2, Sn1, E1, E2) that produced it and write out and label major vs minor elimination products.
(a) State and illustrate the following :(i) Wolff-Kishner reduction (ii) Aldol condensation(b) An organic compound (A) which has characteristic odour, on treatment with NaOH forms two compounds (B) and (C). Compound (B) has the molecular formula C7H8O which on oxidation with CrO3 gives back compound (A). Compound (C) is the sodium salt of the acid. Compound (C) when heated with soda lime yields an aromatic hydrocarbon (D). Deduce the structures of (A), (B), (C) and (D). Write chemical equations for all reactions taking place.
For each pair, predict the stronger nucleophile in the SN2 reaction (using an alcohol asthe solvent). Explain your prediction.(a) (CH3CH2)3N or (CH3CH2)2NH
1. Discuss the role of the Aldol condensation reaction in the synthesis below. What specific reaction was used in the synthesis? What is the importance of the aldol reaction in the entire synthetic approach? 2. Show the detailed reaction mechanism involved in their corresponding specific parts in this syntheses.
Draw a structural formula for the major product of the acid-base reaction shown. You do not have to consider stereochemistry. Do not include counter-ions, e.g., Na+, I-, in your answer. In those cases in which there are two reactants, draw only the product from the compound that reacts.
odine monochloride, ICI, is a reagent whose reactivity mirrors that of other dihalogens (X₂) with nucleophilic πt bonds. Using curved arrows to show the flow of electrons, draw a plausible mechanism for the following transformation. Make sure that your mechanism accounts for the correct stereoselectivity.
Complete the reactions below by providing the proper structure(s) in the boxes. Include stereochemistry wherever necessary. The structures only, no need to draw mechanisms
Please provide a detailed mechanism for the synthesis of dibenzalacetone and say what product would be made if only 1 equivalent of acetone was used!
Suggest a mechanism for reactions 1,2,3,4 of the following series of reactions
Please show the mechanisms that convert compound 1 into compound 2. Thank you!
Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in SN1 and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group.Draw curved arrows to show the movement of electrons in this step of the mechanism.
(19, 8, 1) Specify a synthetic scheme that would produce the compound shown above in the fewest steps possible. Use one of the starting materials shown together with any of the available reagents. Give the number of the starting material followed by the letters of the reagents in the order of their use, for example: 3be.