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- Thank you for the answer, would it be possible to follow the path I have attached as well srarting from methanol ---> CH3Br -----> CH3MgBr-------> (H3C)CH-CH2OH ----> E1 Isobutalenededcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.(please answer all questions) 1) Predict the products from reaction of 1-hexyne with thesereagents: a) One equivalent HBr b) One equivalent Cl2 c) H2 , Lindar Catalyst d) NaNH2 in NH3 , then CH3Br
- The oxygen in water is primarily (99.8%) 16O, but water enriched with theheavy isotope 18O is also available. When a ketone or aldehyde is dissolved inH2O, the isotopic label becomes incorporated into the carbonyl group: R2CPO H2O n R2CPO H2O. Explain.. Given the reaction below: N2(g) + 3H2(g) -----> 2NH3(g) deltaH = -92.6 KJWhat is the value of deltaH for the following reaction? 2NH3(g) -----> N2(g) + 3H2(g)For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yne
- Write reactions of 2-methylbutene-2 with the following reagents: a. KMnO4/ H2O/20 °C; b. HBr.Draw the organic products formed when cyclopentene is treated with each reagent. With some reagents, no reactionoccurs.a. H2 + Pd-Cb. H2 + Lindlar catalystc. Na, NH3d. CH3CO3He. [1] CH3CO3H; [2] H2O, HO–f. [1] OsO4 + NMO; [2] NaHSO3, H2Og. KMnO4, H2O, HO–h. [1] LiAlH4; [2] H2Oi. [1] O3; [2] CH3SCH3j. (CH3)3COOH, Ti[OCH(CH3)2]4, (–)-DETk. mCPBAl. Product in (k); then [1] LiAlH4; [2] H2OComplete the following reaction equations :(i) C6H5Cl + CH3COCl →(ii) C2H5NH2 + C6H5SO2Cl →(iii) C2H5NH2 + HNO2 →