3. Draw out the following products Mg (a) CI THF (b) Name the product Product of...
Starting from 3-methylhex-1-ene 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.**Pay attention to the possibility of rearrangement when your mechanism produces a carbocation. A. H2SO4, H2OB. 1. Hg(OAc)2, H2O; 2. NaBH4C. 1. BH3•THF; 2. H2O2, NaOHD. Br2, CCl4E. Br2, H2OF. HBrG. HBr, ROORH. 1. O3; 2. DMSI. H2, Pt
2. Draw the major product(s) from the reaction of the starting material below with the following reagents: (12 marks) (a) (b) (1) BH3, THF (2) H2O2, NaOH, H2O Cl in excess EtOH (0) I-CI (d) (1) O3. CH CI: (2) Zn, acetic acid (e) (1) (1) OsO4, THF (2) H2S (1) Hg(OOCCH3)2, H2O (2) NaBH4, NaOH, H2O
1. Draw the Most stable chair conformation НО. CI HO OH HOS OH 2. Name following structure: Br 3. Give the major product(s): 1) BHY/THF 2) NaOH, H2O, HẠO Bry/CH,CI;
02 Question (2 points) Draw the product of the following reaction sequence. 1. Mg(s), THF 2. CO2(s) 3.H20+ 1st attempt Part 2 (1 point) What is the term used to describe the polarity reversal that occurs in this synthetic sequence? Choose one: A. organometallic B. charge reversal C. Grignard D. umpolung
Draw each product out based on given: 1.03 2.DMS 3. Na2Cr2O /HsSO /H20 PB13 2-methyl-1-propanol Mg/ether 1. CO2 2. H,09 1. KMnO,/NaOH/H,0 2. H30 SOCI pyridine (CHz) CHCH OH pyridine V Mg/ether 1.CO2 2. H₂O* 1. LiAlH. 2. H2O
Please write neatly. 3. Show the products formed in the tollowing reactions draw two enols 1) Mg. Et O 2) CO2 3) H:O NHz Jo .OTo. 쁘. pyridne CI NH Ci CI 0 SOCl OH heat NH 1) CH3MgBr excess CH, CH, -OCH,C 2) H2O COOMe LIAIH OH Ci 0 3. Show the products formed in the tollowing reactions draw two enols 1) Mg. Et O 2) CO2 3) H:O NHz Jo .OTo. 쁘. pyridne CI NH Ci CI 0...
Predict the products of the following reactions. a. b. c. (1) excess CH Mg! CI (2) H30* (1) DIBAL-H (-78 °C) (2) H30 OCH (1) DIBAL-H (-78 °C) (2) H2O
Predict the products anticipated for the following reactions; 1. EtMgBr/THF 2. NH C/ H2O a. 1. n-BuLi, Et2O 2. NH CI, H2O b. H KCN, HCI C. NaCN, HC d.
Predict the products of the following reaction.1. O3 2. DMS 3. H2O
draw or name structures in 1-3. in the reactions, draw the products or write the reagents Naming: 2) 5 - hydroxy-6-methyl-3,7-dioxo - 5-heptenoic acid DO 3) oH ich Y Reaction : 1) Mor - 1) | -| 1. Mg CI 2. CD 3. NH, C,H, 0. 1.H, OH 2. Br₂ , H₂O 3. PDC 1. MAI 2. H30+ 3. Ts CI 4. LDA