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Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. CI Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LIAIH4 f. PB13 k. CH3 CH2CH, MgBr; then H3 o* b. Н2SO4 g. CrОз, Н,SO4, H,О 1. Cg H5 MgBr (phenylmagnesium bromide); then H3 O+ с. НCI h. NaH m. (CH3)2 CHMGB1: then H3 O+ d. HBr i. CH3MGB3; then H3O* n. Dess-Martin periodinane (DMP) e. SOCI2 j. CH3 CH2MgBr; then H3O+

Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. CI Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LIAIH4 f. PB13 k. CH3 CH2CH, MgBr; then H3 o* b. Н2SO4 g. CrОз, Н,SO4, H,О 1. Cg H5 MgBr (phenylmagnesium bromide); then H3 O+ с. НCI h. NaH m. (CH3)2 CHMGB1: then H3 O+ d. HBr i. CH3MGB3; then H3O* n. Dess-Martin periodinane (DMP) e. SOCI2 j. CH3 CH2MgBr; then H3O+

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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Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3
Transcribed Image Text:Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3
Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available а. LIAIHA f. PBIз k. CH3 CH2 CH2 MGB3; then H3 O+ b. Н2SO4 g. CrОз, Н,SO4, H,О 1. C6H; MgBr (phenylmagnesium bromide); then H3 O+ с. НСІ h. NaH m. (CH3)2 CHMgBr: then H3O+ d. HBr i. CH3MgBr; then H3O+ n. Dess-Martin periodinane (DMP) e. SOCI2 j. CH; CH2 MgBr; then H3O*
Transcribed Image Text:Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available а. LIAIHA f. PBIз k. CH3 CH2 CH2 MGB3; then H3 O+ b. Н2SO4 g. CrОз, Н,SO4, H,О 1. C6H; MgBr (phenylmagnesium bromide); then H3 O+ с. НСІ h. NaH m. (CH3)2 CHMgBr: then H3O+ d. HBr i. CH3MgBr; then H3O+ n. Dess-Martin periodinane (DMP) e. SOCI2 j. CH; CH2 MgBr; then H3O*
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