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- OChem HELP... Draw the conformational structures (chair or boat conformations) for the MAJOR product formed when 1-tert-butylcyclohexene reacts with each of the following reagents. Also, indicate if the product obtained is racemic form. a) Br2, CCl4 b) Br2, H2O c) OsO4, then aqueous NaHSO3 d) ICl e) mCPBA, then H3O+, H20 f) O3, then Me2S (conformational structure not required) g) BH3:THF, then H2O2, HO- h) D2, Pt i) Hg(OAc)2 in THF-H2O, then NaBH4, HO- j) BD3 :THF, then CH3CO2TName the following heterocyclic compounds using systematicnomenclature only:Draw the structures based on iupac name digitally (highly suggest chem-space .com for easy drawing) 1,1-Dibromo-4-isopropylcyclohexane 4-sec-Butyl-2-chlorononane 1.1-Dibromo-4-Pert-Butylcyclohexane
- Give the structure corresponding to following name ? (1R,2R)-trans-1-bromo-2-chlorocyclohexanePlease be clear in your writing. Thanks Represent the structures corresponding to the following names: a) 1-isopropyl-4-methylcyclohexeneb) 3-butyl-2-heptinc) 4-methyl-cyclooctind) trans-3,3-dimethyl-4-propyl-1,5-octadieneShow how to convert cyclopentene into cis-1,2-Cyclopentanediolcompound
- Which alkene would give the product alcohol as shown as themajor product? A) I B) II C) III D) Both I and IIReaction of HBr with 3-methylcyclohexene yields a mixture of four products: cis-and trans-1-bromo-3-methylcyclohexane and cis-and trans-1-bromo-2-methylcyclohexane. The analogous reaction of HBr with 3-bromocyclohexene yields trans-1, 2-dibromocyclohexane as the soleproduct. Draw structures of the possible intermediates, and then explain why only a single product is formed in this reaction.Give the structure corresponding to each name.a. 3-bromo-4-ethylheptaneb. 1,1-dichloro-2-methylcyclohexanec. 1-bromo-4-ethyl-3-uorooctaned. (S)-3-iodo-2-methylnonanee. (1R,2R)-trans-1-bromo-2-chlorocyclohexanef. (R)-4,4,5-trichloro-3,3-dimethyldecane