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- Which undergoes electrophilic substitution on the ring most rapidly? a. b. CHO d. e.Which is the major product?a. Ab. Neither product would likely formc. BRank the nucleophiles in each group in order of increasing nucleophilicity.a. -OH, -NH2, H2Ob. -OH, Br-, F- (polar aprotic solvent)c. H2O, -OH, CH3CO2-
- Synthesize each compound from toluene (CgH,CH3) and any other organic or inorganic reagents. a. CeHsCH2OC(CHa O,N H2N. b. CgH;CHO d. HOOC- -NO2 f. HO. -COOH CHO C. е. g. BrWhat is the major product of the following reaction? A. B. SCH₁ SH NaSCH; DMF C. D. SCH3Choose the most correct set of reagents for the following reactions. 1. ? a O b O C O 으으 OH 2. ? OMe a. 1. MsCl, pyridine; 2. NaOCH3, CH3OH b. 1. HCI, pyridine; 2. NaOCH3, CH3OH c. 1. PCI 3, SOCI2; 2. NaOCH3, CH3OH d. 1. TsCl, pyridine; 2. NaOCH3, CH3OH e. 1. CH3O-, pyridine; 2. H* f. 1. Pl3, pyridine; 2. -OCH3
- 3. What is the л-energy diagram of the Friedel-Craft reaction intermediate? a. b. C. d. AIC13 Arenium ? e. not a.-d.Draw a stepwise mechanism for the following reaction: H,SO Part 1: A. HSO, or B. . H,SO, +. OC. H20 view structure D. SO, view structure Part 2: OA. H,0 В. Н.О C. HO view structure OD. H2 view structure Part 3 out of 4 edit structure ... edit structure ... Gr Next part4. Make the indicated disconnections and, with the polarization of the carbon skeleton in mind, draw the synthons and synthetic equivalents required. a. C. e. ~ to OH Ho b. ~ d. f. OH & or
- 1. CH3CH,O- Na* 2. H*, CH3CH2OH OHWhat is the best reagent to complete this synthesis? 1)???? 2) NaCN HO CN A. PBr, CISIMEB sOCl, MSCI B. C. D.a. 4. What is the major product of the following reaction? os a4.04.0x b. a. C. b. H₂SO4 heat C. d. 5. Which is the second most stable alkene? of, of of of. of ? d. e. not a.-d. e.