
IR = 1739 (s), 1649 (w) ppm 30. Draw the major product resulting from the following...
Provide the major product(s) for the following reactions: Show
Stereochemistry when necessary
HBr Br2 CH2Cl2 HBr Br2 ROOR H20 H2O СН,ОН H30* 1) BH3, THE 2) H2O2, NaOH, H2O 1) Hg(O2CCF3)2 CH3OH 2) NaBH4, NaOH 1) Hg(OAc)2, H20, THF 2) NaBH4, NaOH H2 Pd/C
1. PREDICT THE PRODUCT: Provide the structure of the major product expected from the following reactions or reaction sequences. Make sure you account for any regio- and/or stereochemistry! (24 pts.) H2O 1. Hg(OAC), CH, OH 2. NaBH H2SO4 H20 1) BH-THF 2) H202, KOH HBr Bry, H2O HBr ROOR 1. BH3-THF 2. H2O2, NaOH H20, H2SO4 1. NaNH2 H2 H-CEC-CH2 CH2 CH3 2. CH CH Br Lindlar cat 1. Sia BH-THF 2. H2O2, H2O
1. Please write the chemical structures of the major products (denoted by 1A-10) of the following reactions. 1) og 2) Zn/CH3COOH 1A + 1B 9-BBN, 2 eq. - H2O3, NaOH, H20 $10 Lindlar catalyst H2, catalytic Pd/C 1D 1E CH3CH2OH Hg(OAC)2, H20 H2SO4 NaBH, 1F mo u mom 11 + 13 Lindlar catalyst CH3COH 1K NaNH, in liquid NH3 Pd/C, H2 - 1M IN
3. Predict the major product(s) for the following reactions. (12 points) 1. BH3 THE 2. H2O2 NaOH Br2 H20 1. Hg(OAc)2 CH3OH 2. NaBH4 HBr
Practice: Write the products for the following reactions. Propene Cyclohexene HBr | CH 3 CH Br CH₂ Hert Cl2, CH2Cl2 NBS, H2O, DMSO Cl2, CH3OH 1) Hg(OAc)2, H2O/THF 2) NaBH 1) BHz in THF 2) H2O2, OH-
1. Give the major product of the following reactions, write NR. if no reaction happens. Indicate the stereochemistry if necessary CHCI KOC(CH3). (CH),COH 1. conc. HBr, heat 2. KOBU, HOBU 1. NaOM, MOH CI 2. BICN 1. 1 eq. BH3. THE 2. H2O2, NaOH, H2O 3. Hg(OAC), MeOH 4. NaBH4, NaOH, H2O 1. conc. HCI 2. LDA, THF 3. O. CH,OH 4.(CH), 1. Hg(OAC), THE 2. NaBH, NaOH, H2O > OH (Hint: product has a bicyclic ring)
Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (10 points total) Br HBr CH2CI Br2 HBr Но ROOR CH,OH Н,о н* Н,о° 1) Hg(O,CCF3)2 CH,OH 1) BН, THF 2) H,О, NaOH, Нао 2) NaBH, NaOH 1) Hg(OAc) Н0, THF/ Hа Pd/C 2) NaBH, NaOH
Starting from (R)-3-methylhex-1-yne as the substrate at the center of your page, draw a reaction map showing the regiochemical and stereochemical outcome or outcomes for each of the following series of reagents. Name each of your products, including stereochemical designations for any chirality centers that are generated.A. HgSO4, H2SO4, H2OB. 1. 9-BBN; 2. H2O2, NaOHC. Br2, CCl4D. HBrE. xs HBrF. HBr, ROORG. xs HBr, ROORH. 1. O3; 2. H2OI. H2, Lindlar's catalystJ. Na, NH3
Predict the major organic product
or products of each of the following reactions:
Identify the mechanism
taking place in each of the reactions and please provide
explanation.
H2SO4 a) (CHỊ) CH CH=CH, HO Hg(OAc)2 NaBH4 b) (CH3)2CH CH=CH2 H2O BH3: THE H2O2, NaOH c) (CH3),CH CH=CH2 H2SO4, H2O d) CHCECH HgSO4 HZ/Ni f) + Cl2 + H2O g) Cold KMnO4 dilute h) 1. CH CO-OH 2. Hz0 Br2 i) CC14
3. Identify (draw the structure showing stereochemistry where required) ALL of the missing reactant, reagents, or major product to complete the following transformations. а. Nal НРО, b. H2SO4 Но KMnO4 NH2 d. он Br2 CH2CI2 CHCI кон f. но" 1. excess Hg(OAc)2, H2O/THF OH 2. NaBH g- 1. еxcess BH,/ THF 2.H2O2 h.