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. OH хонь CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H2SO4 g. CrO3, H2SO4, H₂O Reagents available c. HCI h. NaH d. HBr i. CH3 MgBr; then H3O+ e. SOCI₂ j. CH3CH2MgBr; then H3O+ k. CH3CH2CH2MgBr; then H3O+ 1. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP) 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 none Submit Answer Retry Entire Group No more group attempts remain Previous Next

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. OH хонь CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H2SO4 g. CrO3, H2SO4, H₂O Reagents available c. HCI h. NaH d. HBr i. CH3 MgBr; then H3O+ e. SOCI₂ j. CH3CH2MgBr; then H3O+ k. CH3CH2CH2MgBr; then H3O+ 1. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP) 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 none Submit Answer Retry Entire Group No more group attempts remain Previous Next

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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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. ů Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 c. HCI d. HBr e. SOC12 g. CrO3, H₂SO4, H₂O h. NaH Reagents available i. CH3 MgBr; then H3O+ j. CH3 CH₂ MgBr; then H3O+ k. CH3 CH₂ CH₂ MgBr; then H30+ I. C6H5 Mg Br (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP) 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. OH Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 c. HCI d. HBr e. SOC1₂ Reagents available g. CrO3, H₂SO4, H₂O h. NaH i. CH3 MgBr; then H3O+ j. CH3 CH₂ MgBr; then H3O+ k. CH3 CH₂ CH₂ MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP) Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material 4 Reagent for step 1 n Reagent for step 2 j Reagent for step 3 c
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. r Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LiAlH₁ f. PBr3 b. H₂SO4 c. HCI d. HBr i. CH3 MgBr; then H3O+ e. SOC1₂ j. CH3 CH₂ MgBr; then H3O+ g. CrO3, H₂ SO4, H₂O h. NaH k. CH3 CH₂ CH₂ MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+t n. Dess-Martin periodinane (DMP) 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. OH Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 g. CrO3, H2SO4, H₂O b. H2SO4 c. HCI h. NaH d. HBr i. CH3 MgBr; then H3O+ e. SOCl2 Reagents available j. CH3CH2MgBr; then H3O+ k. CH3CH2CH2 MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP)
Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound s synthesis requires only two steps enter "none" for step 3. OH `CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LIAIH4 f. PBr3 k. CH3 CH2 CH2 MgBr; then H3O+ b. Н>SO4 g. CrОз, Н, SO4, H,O 1. C6 H5 MgBr (phenylmagnesium bromide); then H3O+ с. НC h. NaH m. (CH3)2CHMgBr: then H30+ d. HBr i. CH3 MgBr; then H30+ n. Dess-Martin periodinane (DMP) e. SOCI2 j. CH3 CH2MgBr; then H3O+ Write the number/letters of the alchol/reagents in the boxes below.
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. CH2 H3C CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 g. CrO3, H2SO4, H₂O b. H2SO4 c. HCI h. NaH d. HBr e. SOC12 i. CH3 MgBr; then H3O+ Reagents available j. CH3CH2MgBr; then H3O+ k. CH3CH2CH2MgBr; then H3O+ 1. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP)
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. OH Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LiAlH4 f. PBr3 k. CH3 CH₂ CH₂ MgBr; then H3O+ b. H₂SO4 9. CrO3, H₂SO4, H₂O I. CGH, MgBr (phenylmagnesium bromide); then H3O+ c. HC1 h. NaH m. (CH3)2 CHMgBr: then H₂O+ d. HBr i. CH, MgBr; then H3O+ n. Dess-Martin periodinane (DMP) e. SOCI₂ j. CH3 CH₂ MgBr; then H3O+ 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
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. CI `CH3 Alcohol Starting Materials Reagents Available 1. methanol a. LIAIH4 f. PBr3 k. CH3CH2CH;MgBr 2. ethanol b. H2SO4 I. CGH5MGB (phenylmagnesium bromide) g. Cro3 3. 1-propanol c. HCI h. NaH m. (CH3)2CHMgBr 4. 2-propanol d. HBr i. CH3M9BR n. pyridinium chlorochromate (PCC) 5. cyclohexanol e. SOCI, j. CH3CH2M9B 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 Submit Answer Try Another Version 5 item attempts remaining
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 Reagents Available 1. methanol a. LIAIH4 f. PBr3 k. CH3CH,CH,MgBr 2. ethanol I. CgH5MgBr (phenylmagnesium bromide) b. H2SO4 g. CrO3 3. 1-propanol с. НС h. NaH m. (CH3)2CHMgBr 4. 2-propanol d. HBr i. CH;MgBr n. pyridinium chlorochromate (PCC) 5. cyclohexanol e. SOCI2 j. CH3CH2M9B 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. Br Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LIAIH4 f. PBrs k. CH3 CH2 CH, MgBr; then H30+ b. H2 SO4 g. CrO3, H2 SO4, H2O 1. C3 H5 MgBr (phenylmagnesium bromide); then H3O* с. НСI h. NaH m. (CH3)2 CHMgBr: then H30+ d. HBr i. CH;MgBr; then H30+ n. Dess-Martin periodinane (DMP) e. SOCI, j. CH3 CH2 MgBr; then H3O+ Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material Previous Next
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. LIAIH4 f. PBr3 k. CH3 CH2 CH, MGB1; then H3O+ b. I. C,H5 MgBr (phenylmagnesium g. H2 SO4 CrO3, H,SO4, H,O bromide); then H30 + с. НСІ h. NaH m. (CH3)2 CHMGB.: then H3 O+ i. CH3MGB1; then H3O+ d. HBr n. Dess-Martin periodinane (Previous Next