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- How to prepare the following. H3 C CH3 H3 C Br from H3C CH3 НЗС Conly source of carbon)Give IUPAC names for the following structures. When appropriate, abbreviate ortho (o), meta (m), and para (p), no italics, if you elect to use these terms. CH₂CH₂CHCHCHSCHCH₂ I T CH₁ CH₂ 1st structure: CH3 CH3 I 2nd structure: Submit Submit Answer Try Another Version OCH3 CH₂CCH₂ OCH3 10 item attempts remainingWhat is the predicted product of the reaction shown? O & N(CH3)2 | IV (CH3)2NH H₂SO4 1. N(CH3)2 2. H3O+ || ОН HO |||
- Draw the organic product of the following reaction. CH3 m-CICgH,CO;H • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, just draw one stereoisomer. • If more than one product is possible, only draw the major product. opy asteWhat reagent/reagents is/are necessary to transform the starting molecule into the desired product? ?. CH,CH•CHỔH CH3CHWhat reagent/reagents is/are necessary to transform the starting molecule into the desired product? SO3H ?
- (a) 2-methyl-2-pentanol Draw the structure of the alkene that was used to prepare the alcohol in highest yield. AAVIL ? ChemDoodleⓇ Which process does this employ? 1. Hg(OAc)2, H₂O; 2. NaBH4 01. BH3; 2. H₂O2, NaOH OsO4, H₂O2 On n [ ]#19. CH3CH2CHO HCN→ CH3CH₂CH(OH)CNPlease draw out all missing parts of the reaction like as in reagents, products starting materials) H3C CH3 H30", A H,CH,Co OCH,CH;