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You wish to make compound D. You have the starting materials E, F, or G and a range of reagent(s) available to you, as given below. The shortest route is three steps. Outline how you would achieve maximum yield of product D. In your answer clearly note the starting material chosen, the structure of the intermediates and note the reagents you would use to perform each step. HO CH3 'Retrosynthesis arrow' 'Retrosynthesis arrow' 'Retrosynthesis arrow' CH3 ОН step 3 step 2 step 1 D intermediate II intermediate l Starting material E, F or G Starting material (only choose one) HO CH3 CH3 CH3 `CH3 `CH3 `CH3 HO, E F G Reagents and solvents available to you РСС, Н2О Dess-Martin Periodinane, CH2C12 Na2Cr207, H2SO4, acetone LIAIH4, THF NaBHa, MeOН На, Pа/C, MeOН (CH3)3SICI, imidazole, CH2C12 (CH3)2('Bu)SiCl, imidazole, CH2C12 BnBr, NaH, THF Bu4N+F» THF H*/H2O

You wish to make compound D. You have the starting materials E, F, or G and a range of reagent(s) available to you, as given below. The shortest route is three steps. Outline how you would achieve maximum yield of product D. In your answer clearly note the starting material chosen, the structure of the intermediates and note the reagents you would use to perform each step. HO CH3 'Retrosynthesis arrow' 'Retrosynthesis arrow' 'Retrosynthesis arrow' CH3 ОН step 3 step 2 step 1 D intermediate II intermediate l Starting material E, F or G Starting material (only choose one) HO CH3 CH3 CH3 `CH3 `CH3 `CH3 HO, E F G Reagents and solvents available to you РСС, Н2О Dess-Martin Periodinane, CH2C12 Na2Cr207, H2SO4, acetone LIAIH4, THF NaBHa, MeOН На, Pа/C, MeOН (CH3)3SICI, imidazole, CH2C12 (CH3)2('Bu)SiCl, imidazole, CH2C12 BnBr, NaH, THF Bu4N+F» THF H*/H2O

Chemistry
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...
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You wish to make compound D. You have the starting materials E, F, or G and a range of reagent(s) available to you, as given below. The shortest route is three steps. Outline how you would achieve maximum yield of product D. In your answer clearly note the starting material chosen, the structure of the intermediates and note the reagents you would use to perform each step. НО CH3 'Retrosynthesis arrow' 'Retrosynthesis arrow' 'Retrosynthesis arrow' CH3 ? HO, step 3 step 2 step 1 D intermediate II intermediate I Starting material E, F or G Starting material (only choose one) HO CH3 O CH3 CH3 CH3 CH3 `CH3 HO, ОН E F Reagents and solvents available to you РСС, Н2О Dess-Martin Periodinane, CH2Cl2 NazCr207, H2SO4, acetone LİAIH4, THF NaBH4, MEOH На, Pd/C, MeOН (CH3)3SICI, imidazole, CH2C12 (CH:)2('Bu)SiCl, imidazole, CH2C12 BnBr, NaH, THF Bu4N+F» THF H*/H2O
Transcribed Image Text:You wish to make compound D. You have the starting materials E, F, or G and a range of reagent(s) available to you, as given below. The shortest route is three steps. Outline how you would achieve maximum yield of product D. In your answer clearly note the starting material chosen, the structure of the intermediates and note the reagents you would use to perform each step. НО CH3 'Retrosynthesis arrow' 'Retrosynthesis arrow' 'Retrosynthesis arrow' CH3 ? HO, step 3 step 2 step 1 D intermediate II intermediate I Starting material E, F or G Starting material (only choose one) HO CH3 O CH3 CH3 CH3 CH3 `CH3 HO, ОН E F Reagents and solvents available to you РСС, Н2О Dess-Martin Periodinane, CH2Cl2 NazCr207, H2SO4, acetone LİAIH4, THF NaBH4, MEOH На, Pd/C, MeOН (CH3)3SICI, imidazole, CH2C12 (CH:)2('Bu)SiCl, imidazole, CH2C12 BnBr, NaH, THF Bu4N+F» THF H*/H2O
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