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Steps and explanations. Also provide, if possible, ways to adress this kind of problems in general.
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- Classify each carbocation as primary, secondary, or tertiary. a. b. 人 C. d.1.) LIAIH, NH 2.) H3O* a.) b.) c.) но. NH NH Racemic d.) e.) но HODraw 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 aste
- Kk.318.Draw the organic product(s) formed when CH3CH2CH2OH is treated with each reagent. a.H2SO4 b.NaH c.HCl + ZnCl2 d.HBr e.SOCl2, pyridine f.PBr3 g.TsCl, pyridine h. [1] NaH; [2] CH3CH2Br [1] i.TsCl, pyridine; [2] NaSH j.POCl3, pyridineDraw the structures of organic compounds A and B. Indicate stereochemistry where applicable H2 Lindlar's H2O H,O* OH 1. NaNH2 catalyst H-C=C-H compound A compound B 2. CH3CH2CH2Br (1 equiv.)
- 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 remainingExplain why stereochemistry is observed in this compound.( do 4 5 6 7 with exaplanation plz