Draw the organic products formed when 4-octyne is treated with each reagent. a. H2 (excess) + Pd-C b. H2 + Lindlar catalyst c. Na, NH, d. [1] Ogi (2] H,0
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![Draw the organic products formed when 4-octyne is treated with each reagent.
a. H2 (excess) + Pd-C
b. H2 + Lindlar catalyst
c. Na, NH,
d. [1] Ogi (2] H,0](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F6ce87914-8ac3-497c-b6f5-bcf5bcbc6e7d%2F557169f8-e09f-4a70-b5cf-aafb58c8cd37%2F4sj29s_processed.png&w=3840&q=75)
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- 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] H2OSynthesize each compound from toluene and any other organic or inorganic reagents. a. C6HSCH2BR b. C6HSCH2OC(CH3)3 -CHO с. O,N НООС -NO2 d. H,N.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, pyridine
- Draw the products formed when p-methylaniline (p-CH3C6H4NH2) is treated with each reagent. a. HCl b. CH3COCl c. (CH3CO)2O d. excess CH3I e. (CH3)2C = O f. CH3COCl, AlCl3 g. CH3CO2H h. NaNO2, HCl i. Part (b), then CH3COCl, AlCl j. CH3CHO, NaBH3CN1. What is the product of the following reaction? سد A. B. HO [H+] -H₂O (Η کھے D. HO OTell whether each stereogenic isomer is either R or S. Assign the correct priority of each group comnected to the stereogenic cemter. a. b. c,H d. NH2 .S. OCH, "Br HO HS CH
- Which is the major product of this reaction sequence? -OEt 2 NaOEt, ETOH H;SO, (aq) Br 100 °C -OEt он он OA. В. OC. O D. 2These reagents can produce ketones with alkynes A. BH3, THF, H2O2 B. KMnO4 C. O3 D. H2SO4, H2O, HgSO4Br KOH / DMSO 6. b. 2-methyl-1-propanol d. 1,2- a. 2-methylpropene propanediene c. no reaction e. something else! 7. cyclopentanol + NaH + DMSO+ bromopropane à(major product) a. cyclopentene reaction b. propene c. propyl cyclopentyl ether d. no e. something else!! 8. 2-bromo-3-methylbutane + KOH / DMSO à(major product) a. 2-methyl-1-butene d. no reaction b. 2-methyl-2-butene c. 3-methyl-2-butanol e. something else!! 9. 2-chloro-3-methylbutane + KI / DMSO à(major product) a. 2-methyl-1-butene b. 2-methyl-2-butene c. 3-methyl-2-iodobutane d. no rxn e. something else!! 10. (S)-2-iodobutane + NaN; / DMF à (major product) N3 c. f. something else!! а. b. с. d. е. no rxn 11. cyclohexene + NBS/ CCl, / light followed by K* t-butoxide / t-butanol with heating à a. cyclohexene b. 1,3-cyclohexadiene cyclohexane e. something else! c. 1,2-cyclohexadiene d.
- Draw the organic products formed when allylic alcohol A is treated with each reagent.a.H2 + Pd-C b.mCPBA c. PCC d.CrO3, H2SO4, H2O e.(CH3)3COOH, Ti[OCH(CH3)2]4, (+)-DET f. (CH3)3COOH, Ti[OCH(CH3)2]4, (−)-DET g. [1] PBr3; [2] LiAlH4; [3] H2O h.HCrO4−–Amberlyst A-26 resin1. Write the structure of the major organic product for reactions a, b and e? H₂C b. H₂c- CH, CH₂ Cold KMnO, OH A KMnO, H c. CH3CH₂-CH=CH-CH₂CH3 + H₂SO4 →Draw the organic products formed in each reaction. H,N. a. CH;OH, H* OH (CH3),CO. е. H2 OCH,C3H5 Pd-C H CH(CH3)2 H CH(CHa)2 H2N b. CeHsCH,OH, H* HBr но. f. starting material in (e) CH,COOH H CH,CH(CH3)2 [(CH3),COCOLO (CH3CH2);N CF;COOH с. NH,CH2COOH g. product in (e) DCC OH NazCO3 d. product in (b) + product in (c) Fmoc-CI H,N H H20