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Draw the complete synthesis of the compounds Question 44 (10 points) Pick One! Draw the complete,...
Give the complete synthesis 45. b) Give the complete, detailed synthesis for the following structure. You may start with any monofunctional compound with two or fewer carbons, any inorganic reagent that you choose, and benzene, cyclohexane, or cyclohexanone.
Design an effective synthesis for each of the following amino acids starting from the compounds shown on the left. You may also use any monofunctional organic compound containing four or less carbon atoms, and any inorganic reagents in your syntheses.
Please answer question 4 with a full explanation. 4. (9 points) Multi-step synthesis. Devise a synthesis for the target molecule starting from benzene and small alcohols with no more than two carbons. You can use any inorganic reagents necessary target 5. (10 points) Analysis of 'H NMR spectrum. Below is the 'H NMR spectrum of the product from this week's experiment.
6. Devise a synthesis of molecule 1 using compounds A, B, C, and D, compounds A, B and C are your only sources of carbons. You can use any appropriate organometallic and inorganic reagents as long as they are relevant to your synthesis. Show all your steps clearly, Recall: Aldehydes are typically more reactive that ketones. CH3CH2! OHC Php CHME
Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents (14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
Gradescope #4 This question is worth 10 points. Propose a synthesis to produce (20,35)-2,3-dibromobutane from acetylene. You can use any inorganic reagents you'd like. You don't have to draw the mechanism - only provide the reagents needed for each step of your proposed synthesis. Br ??? HEH Br exclusive product
3) Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials. Hint: this synthesis will require you to use ozonolysis and a reaction that starts with the letter DI
This question is worth 10 points. Propose a synthesis to produce (2R,3S)-2,3-dibromobutane from acetylene. You can use any inorganic reagents you'd like. You don't have to draw the mechanism - only provide the reagents needed for each step of your proposed synthesis. Br ??? HH Br exclusive product
Gradescope #4 This question is worth 10 points. Propose a synthesis to produce (2R,3S)-2,3-dibromobutane from acetylene. You can use any inorganic reagents you'd like. You don't have to draw the mechanism - only provide the reagents needed for each step of your proposed synthesis. Br ??? HEH Br exclusive product