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- Draw the products formed when CH3CH2C ≡ C−Na+reacts with each compound. a. CH3CH2CH2Brb. (CH3)2CHCH2CH2Clc. (CH3CH2)3CCld. BrCH2CH2CH2CH2OHe. ethylene oxide followed by H2Of. propene oxide followed by H2OIndicate the product obtained by reacting A and B. A || H3C-S-CH₂ Na* || CH 3 B CH2. C. CH3 H3C CH3Draw 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, pyridine
- Draw the products formed when ethylene oxide is treated with each reagent. a. HBr b. H2O(H2SO4) c. [1] CH3CH2O; [2] H2O d. [1] HC ≡ C−; [2] H2O e. [1] −OH; [2] H2O f. [1] CH3S−; [2] H2Otaken in order to gor the product Please explain the mechanisms/steps1. Classify each substituent as electron donating or electron withdrawing LOCH3 C(CH3)3 OCOCH3 b. CN a. b. a. C.
- Draw the eight constitutional isomers having the molecular formula C5H11Cl.a. Give the IUPAC name for each compound (ignoring R and S designations).b. Classify each alkyl halide as 1°, 2°, or 3°.c. Label any stereogenic centers.d. For each constitutional isomer that contains a stereogenic center, draw all possible stereoisomers, and label each stereogenic center as R or S.3. What product is formed when HO(CH₂) CHO is treated with each reagent? c. Ag₂O, NH OH d. Na₂Cr₂O₂, H₂SO4, H₂O a. NaBH, CH₂OH b. PCC 400Draw the eight constitutional isomers having the molecular formula C5H11Cl. a.Give the IUPAC name for each compound (ignoring R and S designations). b.Classify each alkyl halide as 1°, 2°, or 3°. c.Label any stereogenic centers. d.For each constitutional isomer that contains a stereogenic center, draw all possible stereoisomers, and label each stereogenic center as R or S.