لله - od This B-diketone can be synthesized from cyclohexene and cyclopentanone using an enamine reaction; the following steps are involved: 1. Cyclohexene reacts with NBS to give allyl bromide 1; 2. Allyl bromide 1 reacts with Mg, ether to give Grignard 2; 3. Grignard 2 reacts with CO₂ then H3O+ to give acid 3; 4. Acid 3 reacts with SOC1₂ to give acid chloride 4; 5. Cyclopentanone reacts with morpholine to give enamine 5; 6. Enamine 5 reacts with acid chloride 4 to give adduct 6; 7. Adduct 6 is hydrolyzed to give the product. Draw the structure of acid 3.

لله - od This B-diketone can be synthesized from cyclohexene and cyclopentanone using an enamine reaction; the following steps are involved: 1. Cyclohexene reacts with NBS to give allyl bromide 1; 2. Allyl bromide 1 reacts with Mg, ether to give Grignard 2; 3. Grignard 2 reacts with CO₂ then H3O+ to give acid 3; 4. Acid 3 reacts with SOC1₂ to give acid chloride 4; 5. Cyclopentanone reacts with morpholine to give enamine 5; 6. Enamine 5 reacts with acid chloride 4 to give adduct 6; 7. Adduct 6 is hydrolyzed to give the product. Draw the structure of acid 3.

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

Predict the structural formula of the major product of the reaction of 2,2,3-trimethyloxirane with set of reagents. Q) Me2NH
Provide the name of the product after heptanoyl chloride reacts with propan-1-ol under acidic conditions.
Account for the fact that 2-phenylpropanal is formed rather than its constitutional isomer, 1-phenyl-1-propanone.
The reaction of 2-methyl -1-butanol with potassium permanganate gives chief product O 1-methylbutanoic acid both of them O 2-methylbutanoic acid
Benzene can be hydroxylated by treating it with hydrogen peroxide and a strong acid such as trifluoromethanesulfonic acid (TfOH). Propose amechanism for this reaction
7. Provide the major organic product of the following reaction. x 50% H₂SO4
Using chemical equations, show how can you prepare: 3-pentene-1-ol using propyne and ethylene oxide
the organic compound 2-heptanone, belonging to the ketone family, is responsible for the strong penetrating odor in Roquefort cheeses. Starting from acetylene as the starting reagent, propose a synthesis line with the reaction mechanisms involved for the synthetic obtaining of 2-heptanone and use it as a food additive in analogous cheeses.
21. Develop syntheses for the following compounds. As starting materials, you may use cyclopentanol, alcohols containing no more than four carbon atoms, and any common reagents and solvents. OCH3 -CH3
18) The following reaction undergoes three distinct steps: imine formation, electrophilic aromatic substitution, and decarboxylation. Draw each of the intermediates from each of these three steps as well as the final product. BS NH₂ OH heat
Prepare the following compounds : 1-Starting with benzene or any other reagents , prepare 3-phenyl -1-propanol
Propose a reaction starting material and reagents to prepare diphenyl sulfide in the laboratory. Show all the needed steps in the formation of the product