



Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that...
2. For each reaction below, please draw the starting material or the major (singular) product, including any pertinent stereochemical details. (3 pts each) 1.TSCI 2. K ES 3. Hg(OAC)2, D20 -OH EtsN t-B 4. NaBH4 3. CHBrg 1. HBr ROOR 2. LDA THE Kot-Bu, t-BuOH 1. og 2. Me,s
1. Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. (4 pts each) a. H F b. но OH
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit. 2. For the compound shown in the box to the right, provide an IUPAC compliant name, including all stereochemical details.
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit.
2. Provide conditions for the following reactions mations for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and stereochemical details. Additionally, if the product(s) listed would exhibit op circle it/them. (14 pts) at would give you the optimum yield, and be mindful of ally, if the product(s) listed would exhibit optical activity, HO + enantiomer in the bord for the com HO
1) Reactions. Provide the major product for each reaction sequence, account for stereochemistry 1) PCC, CHCI 2) Bry, acetic acid 3) KOBU, A 4) NaOEI, ETOH, P CO- 5) H30 workup 6) THF, H.COPPA HC CH2 O e .cat. Pd(OAc) cat. PPh. DMF, EIN 2) LDA, THF. -78 °C 3) Chichen H3O* workup 4) NaBH, EtOH, then H3O+ workup 5) cat. TSOH, benzaldehyde (c) L AL SUO TESTE TO 1) cat. H2SO4. A лон 2) O3, CH, Cl, then (CH),...
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...
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
4. Complete the following reactions, providing the proper stereochemistry where required. If more than one product is possible, indicate the major product. a) Bry CH Но b) 1) ВН THF CH3 2) Н,О, NaOH Hа сн, Pd сн, d) Нer ROOR e) RCO H 1) Hg(OAch, H2O 2) NaBH З/19
4. Complete the following reactions, providing the proper stereochemistry where required. If more than one product is possible, indicate the major product. a) Bry CH Но b) 1) ВН THF CH3 2) Н,О, NaOH Hа сн, Pd сн, d) Нer ROOR e) RCO H 1) Hg(OAch, H2O 2) NaBH З/19