Specify both the alcohol starting material and the reagents you would use in each step in a sy synthesis requires only two steps enter "none" for step 3. х OH CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4.2-propanol 5. cyclohexanol Reagents Available a. LiAlH4 f. PBг3 b. H2SO4 C. HCI d. HBr g. CrO3 h. NaH k. CH3CH2CH2MgBr 1. C6H5MgBr (phenylmagnesium bromide) m. (CH3)2CHMgBr i. CH3MgBr n. pyridinium chlorochromate (PCC) e. SOCI₂ j. CH3CH2MgBr 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 sy synthesis requires only two steps enter "none" for step 3. х OH CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4.2-propanol 5. cyclohexanol Reagents Available a. LiAlH4 f. PBг3 b. H2SO4 C. HCI d. HBr g. CrO3 h. NaH k. CH3CH2CH2MgBr 1. C6H5MgBr (phenylmagnesium bromide) m. (CH3)2CHMgBr i. CH3MgBr n. pyridinium chlorochromate (PCC) e. SOCI₂ j. CH3CH2MgBr 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

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 2E

See similar textbooks

Similar questions

What are the primary organic products of hydrolysis of the following molecule? о Select one: a. ethanal and hexanol O b. ethanone and 3-heptanol O c. octanoic acid and ethyl alcohol O d. acetone and 3-heptanol O e. 3-heptanone and ethanol
We know that acetals hydrolyze to the carbonyl compound and the alcohol that formed it What would be the product of the following hydrolysis reaction? H,0* Select one: HO to. HO HO. b. H. H. C. HO HO. OH
Paused Complete the following reactions. 1. +H₂O NaBH mild oxidation Complete the following reactions. 1. Base cat. H3CH2C CH₂CH + H3CH2C- C -CH2CH3 2. OCH3 H3C-C -CH2CH3 + H₂O OCH3 3. 4. CH3 NaBH4 H3CH2C C CH2CH3 + CH3CH2OH 5. mild oxidation
The oxidation of alcohol functional groups provides for a new electrophilic center that can be used in synthesis. Consider this two-step reaction involving an oxidation and a nucleophilic attack and answer the questions that follow.
Finish the indicated reaction by filling in and starting materials, reagents or products as needed
Draw the organic products in each of the following reactions.
What is the product of the following reaction sequence? 1) NaOEt (excess) H,0, H* 1) SOCI, EtO 2) 2 CH,CH,Br heat 2) NH, OEt `NH2 `NH2 `NH2 NH2 В. C. D. A. O A O'B O D MacBook Pro G Search or type URL #3 & * $ E T Y D F G H K * CO
#9
Name the compound required for step 2, to complete this synthesis. 1. Mg, Et,0 HO 2. ? 3. H*, H;0
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 a. LiAlH4 f. PBr3 b. H₂SO4 c. HCI d. HBr e. SOCI₂ g. CrO3, H₂ SO4, H₂O h. NaH Reagents available i. CH3 MgBr; then H3O+ j. CH3 CH₂ MgBr; then H3O+ k. CH3 CH₂ CH₂MgBr; 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 Reagent for step 1 Reagent for step 2 Reagent for step 3
Determine the reagents that would yield show the intermediates. the product.
which if the following alcohols dehydrates with the slowest rate?