? Modify the given carbon skeleton to draw the major product(s). If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. CH3 CH3 Edit Drawing 1) CH,COgH 2) H₂O*
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- 8.35h ? Modify the given carbon skeleton to draw the major product(s). If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. F2 1) BH, THF 2) H₂O₂, NaOH Save for Later CH3 Edit Drawing 80 F3 F4 2 F5 F6 F7 Attempts: 0 of 10 used DII F8 Submit Answer 8 F98.35i ? Modify the given carbon skeleton to draw the major product(s). If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. H₂C CH₂ Save for Later OsO, (catalytic) NMO CH₂ Edit Drawing CH₂ Attempts: 0 of 10 used Submit Answer 81) RCO,H 2) [H₂SO,J. ? Modify the given structure to draw the major product(s). Use the single bond tool to interconvert between double and single bonds. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. OH
- Give the major organic product(s) of the following. Include stereochemistry when applicable. 1) Nal Br a) 2) NaCN, acetone 1) NaOC(CH3)3, heat d Br 2) BH₂ THF; 3) H,O,, NaOH(aq) b) c) d) c) 2) KOC(CH3)3, heat Copyright University of California Merced 2022 Br 1) NaOH, heat 2) MCPBA 1) KOC(CH3)3, heat 2) H3O+Provide the major product of the reaction sequence. If cis/trans isomers are possible, draw only the major isomer. If enantiomers are possible, do not specify configuration. Select Draw Rings More Erase // H 1) Br2, heat 2) 2 equiv. NaCN DMFProvide the major product of the reaction sequence. If cisltrans isomers are possible, draw only the major isomer. If enantiomers are possible, do not specify configuration. Select Draw Rings More Erase C H N 1) Br2, heat 2) 2 equiv. NaCN DMF
- ]>90% e.e. TSOH (cat.), CH,Cl2 then workup racemic но mostly one diastereomer ]5:1 diastereomer mix product after these transformations >90% e.e. 2) a) NANH2, THF, -20 °C b) OHC-CH,CH3 c) workup ]racemic mostly one diastereomer 3) NaH, MegSi-CI, then workup ] 5:1 diastereomer mix product after these transformations2. Complete the following: Stereochemistry and regiochemistry may be important. type a) NaOH (aq) b) neutralize ➤ OMe a) LiAlH4, ether NMe2 f) b) H3O+ type b) a) HS SH ZnCl2, H+ b) Raney Ni g) type formation of thioacetal/desulfurization HO type Hell-Volhard-Zelinsky Reaction h) CO₂Et type Wittig Reaction H H₂N OEt OH DCC, CH2Cl2 Ph type a) NaH, THF CO₂Et d) b) BnBr, THE CO₂Et c) NaOH(aq); HCl(aq); heat type type HO type (COCI)2, cat DMF CH2Cl2 j) CI type a) NHEN b) LiAlH, THE c) H3O+ CO₂Me CO₂MeDraw the product(s) of bromination. Br, (a) Br Br Br Br H. H.
- When a new center of chirality is created, isomers can result. For the reaction below, specify the kinds of isomers that are produced and in what ratio they form. (For reactions you are not already familiar with, products are shown without stereochemistry.) H₂C. Cl₂ Submit Answer The product(s) of this reaction is (are hv Retry Entire Group 2-chloroisomer(s) only a single achiral compound with no chiral centers a single meso compound a single chiral compound two achiral diastereomers in unequal amounts two enantiomers in equal amounts (a racemate) two enantiomers in unequal amounts two chiral diastereomers in equal amounts two chiral diastereomers in unequal amountsWhat 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 + enantiomer8.35d Modify the given carbon skeleton to draw the major product(s). If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. H3C H3C- 1) OsO4 2) NaHSO /H₂O 8.35e Save for Later -CH3 Edit Drawing Attempts: 0 of 10 used Submit.