By means of a series of equations outline a method for carrying out the ff. conversions. You may use reagents you wish. More than one step maybe required. a. acetylene b. cyclohexanone c. ethyl bromide athanol +methylcyclohexanol acetaldehyde hongon honul othenel
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- 1. Using Br2 in C2H4Br2 will result in HBr and ______. a. C2H3Cl3 b. C2H4Cl3 c. C2H2Cl3 d. none of the above 2. How many halogenation are posible in propane? a. 3 b. 8 c. 6 d. 10 3.Sulfonation of pentane will result in ________ and water. a. C5H11SO3H b. C5H12SO3H c. C5H14SO3H d. none of the above 4.Nitration of hexane will result in ________ and water. a. C6H13SO3H b. C6H15NO2 c. C6H13NO2 d. C6H14NO2 5.How many moles of O2 in heating a C12H26 (dodecane) a. 27 b. 37 c. 24 d. none of the above2-methyl-1-propanol heated with acidic K2Cr2O7 reactionhttps://www.bartleby.com/questions-and-answers/4.-what-carbonyl-compounds-give-the-following-alcohols-on-reduction-with-liaih4-show-all-possibiliti/57dd480d-13a9-449b-891a-67217d3799f1
- Percent yield: 68 melting point:115-122 what is the lit melting point for this product? Did you successfully make pure 2,3-Diphenylquinoxaline? ExplainChoose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acidSolution:- 3. Determine the amount, in of a (2.20 M s olution of dichloromethane needed to completely react with 15.72g cyclohexene to give 1,2-dibromocuclohexanw. Assume 12% excess is needed in order to react completely. a . How much 1,2 -dibromocyclohexane would theoretically be produced ? c. How many ML of the 2.20 M Br2 solution are required?
- tert-butyl chloride (2-chloro-2-methylpropane) from tert- butyl alcohol (tert-butanol) using an acid catalyzed dehydration reaction Physical Constants Compound Mol. Wt (g/mol) Density (g/mL) b.p. (°C) m.p. (°C) 2-Methyl-2-propanol 74.12 0.786 82 25 2-Chloro-2- methylpropane 92.57 0.851 51 -25 Hydrochloric acid 37% soln in H2O 1.18 -85 -26 12.0ml of t-butyl alcohol, with 25.0ml 12.0M HCl, 12ml of water, 12ml of saturated aqueous sodium bicarbonate, 12ml of saturated aqueous sodium chloride, magnesium sulfate Typically yield 6.34g How would I calculate theoretical and percent yield for the reaction ? Please and thank you!tert-butyl chloride (2-chloro-2-methylpropane) from tert- butyl alcohol (tert-butanol) using an acid catalyzed dehydration reaction Physical Constants Compound Mol. Wt (g/mol) Density (g/mL) b.p. (°C) m.p. (°C) 2-Methyl-2-propanol 74.12 0.786 82 25 2-Chloro-2- methylpropane 92.57 0.851 51 -25 Hydrochloric acid 37% soln in H2O 1.18 -85 -26 12.0ml of t-butyl alcohol, with 25.0ml 12.0M HCl, 12ml of water, 12ml of saturated aqueous sodium bicarbonate, 12ml of saturated aqueous sodium chloride, magnesium sulfate 1 (CH3)COH + 1 H3O^+ Cl^- -> 1 (CH3)3CCl + 2 H2O Typically yield 6.34g Why is the percent yield be lower than expected? 53.9% .. Is it due to evaporation? Is it not the major product? If this reaction was with 2-butanol/HCl instead of tert butanol, how would I obtain the products/mechanism, and determine major products? Thank you!!tert-butyl chloride (2-chloro-2-methylpropane) from tert- butyl alcohol (tert-butanol) using an acid catalyzed dehydration reaction Physical Constants Compound Mol. Wt (g/mol) Density (g/mL) b.p. (°C) m.p. (°C) 2-Methyl-2-propanol 74.12 0.786 82 25 2-Chloro-2- methylpropane 92.57 0.851 51 -25 Hydrochloric acid 37% soln in H2O 1.18 -85 -26 12.0ml of t-butyl alcohol, with 25.0ml 12.0M HCl, 12ml of water, 12ml of saturated aqueous sodium bicarbonate, 12ml of saturated aqueous sodium chloride, magnesium sulfate 1 (CH3)COH + 1 H3O^+ Cl^- -> 1 (CH3)3CCl + 2 H2O Typically yield 6.34g How would I calculate theoretical and percent yield for the reaction ? Please and thank you!
- tert-butyl chloride (2-chloro-2-methylpropane) from tert- butyl alcohol (tert-butanol) using an acid catalyzed dehydration reaction Physical Constants Compound Mol. Wt (g/mol) Density (g/mL) b.p. (°C) m.p. (°C) 2-Methyl-2-propanol 74.12 0.786 82 25 2-Chloro-2- methylpropane 92.57 0.851 51 -25 Hydrochloric acid 37% soln in H2O 1.18 -85 -26 12.0ml of t-butyl alcohol, with 25.0ml 12.0M HCl, 12ml of water, 12ml of saturated aqueous sodium bicarbonate, 12ml of saturated aqueous sodium chloride, magnesium sulfate 1 (CH3)COH + 1 H3O^+ Cl^- -> 1 (CH3)3CCl + 2 H2O Typically yield 6.34g Why is the percent yield be lower than expected? 53.9% .. Is it due to evaporation? What is the major product of this reaction? isobutene or t-butylchloride? If this reaction was with 2-butanol/HCl instead of tert butanol, how would I obtain the products/mechanism (SN2?), and determine major products? If sn2, why? Thank you!! This was…Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) Br2, FeBr3 Na/NH3, -33 degrees C NBS, light KMnO4, H3O+ Mg metal, ether KOH, EtOH, heatFill in necessary products reactants or reagants of these reactions. Please note the existence of enantionmers in some cases.