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 step3.Alcohol Starting Materials1. methanol2. ethanol3. 1-propanol4. 2-propanol5. cyclohexanolReagents availablea. LiAlH4 f. PBr3k. CH3 CH₂ CH₂ MgBr; then H₂O+b. H₂SO4 g. CrO3, H₂SO4, H₂OI. C6H5 MgBr (phenylmagnesium bromide); then H3O+c. HC1h. NaHm. (CH3)2 CHMgBr: then H₂O+d. HBri. CH3 MgBr; then H3O+n. Dess-Martin periodinane (DMP)e. SOCI₂j. CH₂ CH₂ MgBr; then H3O+Write the number/letters of the alchol/reagents in the boxes below.Alcohol starting materialReagent for step 1Reagent for step 2Reagent 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.OHAlcohol Starting Materials1. methanol2. ethanol3. 1-propanol4. 2-propanol5. cyclohexanolReagents availablea. LiAlH4 f. PBr3k. CH3 CH₂ CH₂ MgBr; then H3O+b. H₂SO4 9. CrO3, H₂SO4, H₂OI. CGH, MgBr (phenylmagnesium bromide); then H3O+c. HC1h. NaHm. (CH3)2 CHMgBr: then H₂O+d. HBri. CH, MgBr; then H3O+n. Dess-Martin periodinane (DMP)e. SOCI₂j. CH3 CH₂ MgBr; then H3O+Write the number/letters of the alchol/reagents in the boxes below.Alcohol starting materialReagent for step 1Reagent for step 2Reagent for step 3

In the Jones oxidation, secondary alcohols are oxidized to ketones while primary alcohols undergo…

3. Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 g. CrOs, H₂SO4, H₂O c. HCI h. NaH d. HBr i. CH3 MgBr; then H3O+ e. SOCI₂ j. CH₂ CH₂ MgBr; then H₂O+ Write the number/letters of the alchol/reagents the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3 Reagents available k. CH3 CH₂ CH₂ MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H₂O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP)

3. Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 g. CrOs, H₂SO4, H₂O c. HCI h. NaH d. HBr i. CH3 MgBr; then H3O+ e. SOCI₂ j. CH₂ CH₂ MgBr; then H₂O+ Write the number/letters of the alchol/reagents the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3 Reagents available k. CH3 CH₂ CH₂ MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H₂O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP)

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

Chapter19: Enolate Anions And Enamines

Section19.9: Crossed Enolate Reactions Using Lda

Problem JQ

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