e. SOCl2 j. CH3 CH2MgBr; 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 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)

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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e.
SOCl2
j. CH3 CH2MgBr; 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
Transcribed Image Text:e. SOCl2 j. CH3 CH2MgBr; 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
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)
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. 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)
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