Draw the products of the two step reaction sequence shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.
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- 2. Fill in the major product of the following reactions. Include stereochemistry when appropriate. all ebuloni abnucqmoo privolial arts to atinja intel -omoid-S-(3) ensilexeromond-4-(S) on KOtBu tBuOH ya CI KOtBu tBuOH CI NaOMe MeOH NaOMe MeOH EtOH CI MeOH benogoto to is heat congid of evol mon aheat malwollot erti (teawol ediompounds and Ulteleleh Spectroscopy - E Draw the organic product(s) you would expect from the following reaction. O Visited nd Exit • You do not have to consider ● - stereochemistry. You do not have licitly draw H atoms. (+ Previous 7 1.03 2. Zn 90-85 Next ?please show the detailed mechanism for each step for the reaction below. OTBDPS Me TMANO (anhydrous) (6 equiv) Co (CO) CH,Cl, -78 °C to r.t. 85% H. Me ОТВОPS triquinane
- 1. Draw the intermediates A-C for reactions a and b. Please show the appropriate stereochemistry where necessary. RO hv .. RQ CO₂Me MO,C. Anti-tumour agent Coriolin co₂Me barreleneWhat reagents are appropriate to carry out the conversion shown? - OH LOM 1. mCPBA; 2. CH3MgBr; 3. H₂O O 1. CH3MgBr; 2. H₂O O 1. mCPBA; 2. H₂O O mCPBA + enantiomerUse the References to access important values if needed for this question. Draw the structure of the product that is expected when the following compound is treated with concentrated H2SO4. он H2S04 ? heat CH3 You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. ited opy Bste [F CH4 ChemDoodle Retry Entire Group 3 more group attempts remaining Submit Answer Previous Next Email Instructor Save and Exit Cengage Learning | Cengage Technical Support
- Which conditions will produce the target product in the highest yield? O A) 1. BH3; 2. H₂O₂, NaOH, H₂O B) 1. OsO; 2. S(CH3)2 C) 1. Hg(OAc)₂, H₂O; 2. NaBH4 D) H₂SO4, H₂O A ? B OH racemic mixturec. Snl reactions dominate under polar protic solvents. Increasing the polarity of the solvent will increase the rate of the reaction because the polar solvent will stabilize the dispersed charges on the transition state more than it will stabilize the neutral reactant. Label areas of ô* and & on the molecules of the transition state of the SN1 reaction below: Me Me Ме Me Me H20 Br -Br OH + НО \'H Et Et RDS Et H Et Et transition state not isolable carbocation intermediate not isolable18. Provide the major product or products in the boxes below. Be clear about the stereo- and regiochemistry of all products. 1. Hg(OAc), H20 1. ВН THF conc. HPO4 heat 2. HОд NaOH 2. NaBH, Br2 1,1,2-trimethylcyclohexane ELONA/ELOH hv heat 1. Og -78 °C 2. Me,s
- Draw the major expected product of the reaction. Clearly show stereochemistry in the product by drawing one wedged bond, one hashed bond and two in-plane bonds per stereocenter. of KOC(CH3)3 HOC(CH₂) Select Draw Templates More / | || F C H CI Erase Q2 Q Question Source: Vollhardt 7e Organic Chemistry: Structure And Function Publisher: W.H. Freem1. Write the correck IUPAC nemes Far the Foilawing organic comPounds: Br CH3 H3C 8. Assign E an or Z configuration bi CI 2. CidssiFy the Following reagents cs either nucleaphiles or e lectraph:les: Zn, CH3NH2, HS, OHa, CH3COOH, HoSO 3. Whet are the products obtained From the addition of HBr to each of the falbuing compounds? CH3 a) + HBr > CHo +HBr- 2.Y Part B Identify which reagent should be used to form the following product: View Available Hint(s) 1. mCPBA. 2. H₂O, H₂SO, O H₂O, H₂SO, 1. Os0₁. 2. NaHSO O1 Hg(OAca), H₂O. 2. NaBH. Submit Y ? W
