Provide all organic products for the reactions below. Indicate the relationship between any stereoisomers (label as diastereomers or enantiomers).
Provide all organic products for the reactions below. Indicate the relationship between any stereoisomers (label as...
1. Give the major product of the following reactions, write N.R. if no reaction happens. Indicate the stereochemistry if necessary: h. 1. Cl2, H2O 2. KOtBu 1. NaOH, H20 2. PCC НО i. 1. ICH2Znl, Et2O 2. MSCI, pyr 3. LDA ОН j. 1. HВг, "BuOOH, hv 2. NaCN, DMF
Organic Chemistry Help (2) Provide products for each of the reactions below. Show all enantiomers and/or diastereomers. Circle any meso compounds that are produced. (1) BDs, THF (2) NaOH, H202, THF- H20 (1) BD3, THF (2) NaOH, H202 THF- H20 OsO4, NMO, THF-H20 HCI ether
1) Provide the starting material for the following reaction. (0.5 pts) Он Он 1) Hg(OAc)2, H20 2) NaBH (provide starting material) 2) Provide the major organic product(s) for the following reactions. If stereoisomers are formed, please show both stereoisomers. (0.5 pts each) 1) BH3 THF a) 2)120 NaOH 1) NaOH, H-O, 55°C b) 2) OsO4 t-BuOOH 1-BuOH, NaOH Br2 c) CCl4 H2O, H2SO d) H9SO4 2 equivalents HBr e) 3) The following ction generates an ether. Provide the major organic...
stereoisomers of the following below. Label all chirality, indicate any enantiomers and/or diastereomers. a. Amino Acid Leucine CH,CHCH2çit code CH3 ENita b. 2-methyl-1-cyclohexanol
2. Draw, in the provided spaces/ boxes, the major organic products of the following transformations. Be sure to indicate appropriate stereochemistry. If the reaction generates enantiomers, draw one and write tenantiomer' 1. Cl2, H20 2. NaOH На Pd/C 1.Hg(OAc)2 CH,OH 2. NABH 1. CH CO H 2. Hао* Н,с" HC @) 1. ВНа, THF 2. H202, NaOH Br2 CH2CI2 (E)-5-methylhept-3-ene MeOH conc'd H3PO4 ОН Br NAOCH3
Topic: Organic Chemistry Please make all drawings very clear. Please show all work and side products along with brief explanations. Thank you. 2. Fill in each box with the expected organic product of the indicated multistep transformation. Be sure that each product you draw takes into account all steps of the transformation, including workup steps! Remember to account for stereochemistry where appropriate. он 1. CrO2, H20 2. MeOH, H+ cat. 1. HNEt2, pyridine 2. LiAlH4, Et20 3. H* workup NMez...
1. Predict the major organic products of the following reactions. Draw all stereoisomers that are formed. НО, OH 1 eq ,H2SO4 (assume H2O workup of reaction to neutralize product) 1. LDA 2. (assume H,O workup of reaction to neutralize product) 3. Hg(OAC)2 4. NaBH, EtOH 1eq HBr EtOH ambiente 1. Brz. CCL 2. NaOET, ETOH OH
6. (60 pts) Provide the major organic product(s) of the reactions below, including any stereoisomers formed in substantial amounts. You may write ‘racemic’ to indicate a pair of enantiomeric products. Assume that all the chiral starting materials are single enantiomers. 1) KOIBU 8 2) Og, then S(CH3)2 1) O 2) H.02 e 1) NaP, NH, (0) 2) C1, CH2Cl2 PBrg, Pyridine é 8 3 1) NaN 2) H2O
Using the list, propose the forward synthesis of the retrosynthesis shown below (any number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. НО. OH A. CUCI, 0 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. CuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C G. Br2, FeBr3, THF, 65...
Draw the structure of the final product(s) of this series of reactions 1pt ernces 1 pt 1. Br 1 pt 2.3 equivalents of NaNH 3. mild acid 1 pt 4. BH 5. H202/ NaOH 1 pt 1 pt 1 pt Use the wedge/hash bond tools to indicate stereochemistry where it exists Include H atoms at chiral centers only If a group is achiral, do not use wedged or hashed bonds on it Draw organic species only. Do not include lone...