Draw the major elimination and substitution products formed in this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. Br CH3ONA, CH3OH heat Draw One of the Major Products G
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- Treatment of 1,2-dimethylcyclopentene with OsO4 with NMO produces which of the following? 1 OH CH3 CH3 OH OI O II ||| OIV OV OH CH3 A || OH CH3 OH CH3 H CH3 CH3 ..H for OH CH3 IV CH3 ..H H CH32. 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 ediDraw the structure of the expected major organic product for each of the following five (5) questions. Specify stereochemistry clearly, if relevant. A. CH3 excess Na NH3 (1) H3C-C=C- -CH3 H, cat. Ni,B H3C-C=C С. PB33 H3C° HO, CH D. PhS Na product from reaction 1C Е. OH CH3 H;PO4 ""CH3 B.
- Phm Phn -ph Provide the reagent necessary to Synthes13e the Compounds in 9 myltistep Synthesi3 - Use Autecting groups when necessary. Provide the reagunt heassary to 5 yn the s13e the Compounts 59 mylti step Synthe sis . Use prstectmy grups when nelessary:) Predict the NAME, STRUCTURE and STEREOCHEMISTRY of the BEST ORGANIC REACTANT or the MAJOR ORGANIC product for the following reactions: CH2 МСРВА, НзО* meso 3,4-hexane diol FoH H+OH CHCH a) (name, str, stereochem) ? HCI b) 3-methyl 1-pentene - ? (name, str, stereochem) c) methylcyclohexane ----Br2, hv------? (name, str, stereochem) 40H d) ? (name, str., stereochem) Os04, water----meso cyclohexane 1,2-diol ----1. For the following reactions, predict the major product. lio perox des). peroxidas H2504 H20 supply reaganto Bra Luhuw stereochemistry) NaI Be acetanc MCPBA
- Use 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 SupportExplainwhythefollowingdeuterated1-bromo-2-methylcyclohexaneundergoes dehydrohalogenation by the E2 mechanism, to give only the indicated product. Two other alkenes are not observed.22. Synthesis! Using alkanes and/or cycloalkanes of six carbons or fewer (as your source of carbons) synthesize the following compounds. A Br one consiating of tully conjugated alkes 26.Provida the major productiS for each step in the ong Stereochemistry where i s policable. ueimerioolpen bns ylaimerlaosrela gniworle woled enoilosen ar) to alouborg art eliW.AS tlons e how bemot el tomoitnens ne ti 1emoitnene " elhw vem uoy EON heat ОН
- 34. Draw the major organic product(s) for the following reactions; (*) must include correct stereochemistry; double-dagger (+) must show two products. HBr (a)* Br HBr Br (b) + (1.00 equiv.) Br Br HBr (c)* HCI (d) 48% wt. HBr 37% wt. HCI HEAT OH [H2SO]/ H20 (g) OCH3 [H2SO,]/A CH,OH (excess) (h) [H,SO,1/H20 OH (i)* [H2SO,] / H,0 OH 13What is the name of the following compound +1 Br Brill.. |||| OH₂ OH₂ Co Br H₂O OH₂ trans-teraaquadibromocobalt(1) bromide trans-teraaquadibromocobaltate(1) bromide Ocis-teraaquadibromocobalt(1) bromide cis-teraaquadibromocobaltate(1) bromideO Depart x Fall 20 x 101 Chem x b My Qu x DL Home x + O https://app. 101edu.co A To ... Question 18 of 24 Submit What reagents are required to convert tert-butylbenzene to p-tert- butylbromobenzene? Br А) HBr B) Br2 C) Br2, FeBr3 HC CH3 CH3 CH3 CH3 D) HBr, H2SO4 2:13 PM O Type here to search 底 80% 54°F 3/17/2022 OVO C PrtSc Insert Delete F3 F4 F5 F6 F7 F8 F9 F10 F11 F12 * %23 &