E. Cis-2-pentene Preamble: A student chemist in an attempt to synthesise compound B from the aromatic aldehyde. Use the flow equation to answer Q25-28 сно NH 3 H2, Ni A -H20 60 °C, 90 atm 23. Predict the chemical name of compound B A. p-chlorobenzslamine B. 4-bromoaniline C. benzylamine D. p-chloronitrile E. p-chlorobenzaldehvde mam
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- Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(C2H5)3). 3SnCl4 + 4AI(C2H5)3 →3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.160 L of SnCl4 (d = 2.226 g/mL) was treated with 0.346 L of triethylaluminum (Al(C2H5)3): d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C2H5)4)? If 0.257 L of tetraethylstannane (d= 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides.One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(C2H5)3). 3SnCl4 + 4Al(C2H5)3 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.230 L of SnCl4 (d = 2.226 g/mL) was treated with 0.396 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). If 0.335 L of tetraethylstannane (d = 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?(a) How will you carry out the following conversions?(i) Acetylene to Acetic acid (ii) Toluene to m-nitrobenzoic acid(iii) Ethanol to Acetone(b) Give reasons :(i) Chloroacetic acid is stronger than acetic acid.(ii) pH of reaction should be carefully controlled while preparing ammonia derivatives of carbonyl compounds.
- In this study, the researcher compared S N 2 and E2reaction rates for four substrates. Three of the substrates had a second halogen on the bposition in the molecule. This work also compared the behavior of two nucleophiles:dianion I and II. You should read the abstract and look at Scheme 1 (p. 3082) and Table 4(p. 3086). Abstract: The gas-phase reactions of benzoate and phenolate containing dianions with a series of ‚-substitutedalkyl bromides (X-CH2CH2Br, X ) H, F, Cl, Br) have been studied in a quadrupole ion trap mass spectrometer.Branching ratios between SN 2 and E2 products were measured and rate constants were determined. The‚-halogens increase both the S N 2 and E2 rates, but the effect is greater for the latter process and thereforethese substituents lead to an increase in the amount of elimination. The kinetic data for the SN 2 reactions canbe analyzed via a two-parameter, linear free-energy relationship and the results indicate that field-effects (i.e.,electron-withdrawing…In this study, the researcher compared S N 2 and E2reaction rates for four substrates. Three of the substrates had a second halogen on the bposition in the molecule. This work also compared the behavior of two nucleophiles:dianion I and II. You should read the abstract and look at Scheme 1 (p. 3082) and Table 4(p. 3086). Abstract: The gas-phase reactions of benzoate and phenolate containing dianions with a series of ‚-substitutedalkyl bromides (X-CH2CH2Br, X ) H, F, Cl, Br) have been studied in a quadrupole ion trap mass spectrometer.Branching ratios between SN 2 and E2 products were measured and rate constants were determined. The‚-halogens increase both the S N 2 and E2 rates, but the effect is greater for the latter process and thereforethese substituents lead to an increase in the amount of elimination. The kinetic data for the SN 2 reactions canbe analyzed via a two-parameter, linear free-energy relationship and the results indicate that field-effects (i.e.,electron-withdrawing…In this study, the researcher compared S N 2 and E2reaction rates for four substrates. Three of the substrates had a second halogen on the bposition in the molecule. This work also compared the behavior of two nucleophiles:dianion I and II. You should read the abstract and look at Scheme 1 (p. 3082) and Table 4(p. 3086). Abstract: The gas-phase reactions of benzoate and phenolate containing dianions with a series of ‚-substitutedalkyl bromides (X-CH2CH2Br, X ) H, F, Cl, Br) have been studied in a quadrupole ion trap mass spectrometer.Branching ratios between SN 2 and E2 products were measured and rate constants were determined. The‚-halogens increase both the S N 2 and E2 rates, but the effect is greater for the latter process and thereforethese substituents lead to an increase in the amount of elimination. The kinetic data for the SN 2 reactions canbe analyzed via a two-parameter, linear free-energy relationship and the results indicate that field-effects (i.e.,electron-withdrawing…
- 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…Benzene, C6H6 undergoes substitution reaction with concentrated nitricacid, HNO3 to produce compound L. The reaction of compound L withbromine, Br2 in the presence of iron tribromide, FeBr3 produced compoundM. Benzene also undergoes Fridel-crafts alkylation reaction withchloroethane, CH3CH2Cl using catalyst N to produce compound P (i) Draw the structural formula of L, M and P (ii) State catalyst N. (iii) Show the formation of electrophile that will be reacted with benzene for theformation of compound P.Doxaprost, an orally active bronchodilator patterned after the natural prostaglandins , is synthesized in the following series of reactions starting with ethyl 2-oxocyclopentanecarboxylate. Except for the Nef reaction in Step 8, we have seen examples of all other types of reactions involved in this synthesis. Q. Write equations to show that Step 6 can be brought about using either methanol or diazomethane (CH2N2) as a source of the -CH3 in the methyl ester.
