6. Provide reasonable step-by-step mechanisms for the following reactions. Use arrows to indicate themovement of electrons.a.HNa:OH(catalytic)H₂O(solvent)b.:Br:CH3OHA+O:OH:OHснонCH3OH2 :Br:

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Answered: 6. Provide reasonable step-by-step…

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 b. H₂SO4 c. HCI d. HBr e. SOCI₂ Reagent for step 2 Reagent for step 3 Reagents Available f. PBr3 g. CrO3 h. NaH i. CH3MgBr j. CH3CH₂MgBr k. CH₂CH₂CH₂MgBr I. C6H5MgBr (phenylmagnesium bromide) m. (CH3)2CHMgBr pyridinium chlorochromate (PCC) Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material Reagent for step 1 Pa
3. Write the structure of the product from the first step (Product-1) and then the product from the second step (Product-2) for the two-step reaction sequence shown below. 4 NaBH, Hg(OAc)2 THE / H,O Product-1 Product-2
OH SYNTHESIS 1. POCI3 2. HBr, ROOR 3. Mg, ether 4. benzaldehyde 5. H3O+ workup 6. PCC 7. CH3MgBr 8. H3O+ workup Br T
In which case is it correctly given which reagents should be above the arrows in the reaction given below?
Ff.306.
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
4. Fill in the missing species for the following reactions: a. b. d. H₂C H₂C CH₂ .OH CH₂ OH H₂SO PDC CH₂Cl₂ CH₂₂ Zn(Cu), ether H₂C H₂C H₂C Na₂Cr₂O₂, H₂SO, H₂O las+ CH3 CH3 Wilkinson's Catalyst Benzene H₂C CH₂ H CH3 CH₂ MULTICY
Complete the reactions by predicting the product/s: Zn + 2HC1 –→ ZnH2 + Cl2 b. ZnCl2 + H2 C. no reaction a.
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
Give detailed Solution with explanation

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6. Provide reasonable step-by-step mechanisms for the following reactions. Use arrows to indicate the movement of electrons. a. H Na :OH (catalytic) H₂O (solvent) b. :Br: CH3OH A + O:OH :OH снон CH3OH2 :Br: