
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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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
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
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