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`CH3Alcohol Starting MaterialsReagents Available1. methanola. LIAIH4f. PBr3k. CH3CH2CH;MgBr2. ethanolb. H2SO4I. CGH5MGB (phenylmagnesiumbromide)g. Cro33. 1-propanolc. HCIh. NaHm. (CH3)2CHMgBr4. 2-propanold. HBri. CH3M9BRn. pyridinium chlorochromate (PCC)5. cyclohexanole. SOCI,j. CH3CH2M9BWrite the number/letters of the alchol/reagents in the boxes below.Alcohol starting materialReagent for step 1Reagent for step 2Reagent for step 3Submit AnswerTry Another Version5 item attempts remaining

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ify 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 hol Starting Materials Reagents Available ethanol a. LIAIH4 f. PBr3 k. CH;CH,CH,MgBr hanol b. H2SO4 g. Cro3 I. CGH5MGB (phenylmagnesium bromide) propanol с. HС h. NaH m. (CH3)2CHMGB. propanol d. HBr i. CH;MgBr n. pyridinium chlorochromate (PCC) "clohexanol e. SOC, j. CH3CH,MgBr e 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 bmit Answer Try Another Version 5 item attempts remaining

ify 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 hol Starting Materials Reagents Available ethanol a. LIAIH4 f. PBr3 k. CH;CH,CH,MgBr hanol b. H2SO4 g. Cro3 I. CGH5MGB (phenylmagnesium bromide) propanol с. HС h. NaH m. (CH3)2CHMGB. propanol d. HBr i. CH;MgBr n. pyridinium chlorochromate (PCC) "clohexanol e. SOC, j. CH3CH,MgBr e 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 bmit Answer Try Another Version 5 item attempts remaining

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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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. 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
22. Place the letter for the best reagent to complete each step of the reaction below. Place the capital letter in the box provided. OH OH 0 CH3 CH3 CH3 CH3 OH OCH CH A. 1. NaOCH B. 1. CH₂Br C. MCPBA D. NaCr₂O,, H E. H,O', heat 2. H₂O 2. Mg, ether 3. H₂O
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18. Which of the alkyl halides undergoes faster solvolysis with ethanol (CH3CH2OH)? Br H3C Br H,C- CHo (1) (2) Br Br H,C CH3 CH ( 3) ( 4) а. 3 b. 4 O c. 1 d. 2
Cheto
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7. Provide the major product for the following reaction. Br 1. Mg/THF 2. 3. H₂O H
Which of the following compounds produce the 3 products shown on reaction with KMnO4 and acid (H+). a. I b. II c. III d. II and III
12. Draw the structure of the major organic product(s) for the following reactions and name the reaction. CH3 N-CH3 CI CH3 heat a. (name of reaction) 0- N-CH3 CI CH3 b. (name of reaction) -NH2 + CH3CH2Cl c. (name of reaction) heat NaOH 2 H d. name of reaction H3C e. name of reaction CH3 1. EtQ Na+ 2. H2O, HCI
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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. 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