Analytical and thermodynamic studies on some halogenated benzenoid compounds

The bromination of 2-fluorophenol, 3-fluorophenol, 4-fluorophenol, 2-fluoroaniline, 3-fluoroaniline and 4-fluoroaniline was carried out inaqueous medium using an acidified mixture of potassium bromate andpotassium bromide as a source of bromine. The chlorination of thesecompounds was carried out usi...

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Main Author: Mohran, Hossnia Saber
Published: Royal Holloway, University of London 1986
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547
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spelling ndltd-bl.uk-oai-ethos.bl.uk-7043742018-07-09T15:12:44ZAnalytical and thermodynamic studies on some halogenated benzenoid compoundsMohran, Hossnia Saber1986The bromination of 2-fluorophenol, 3-fluorophenol, 4-fluorophenol, 2-fluoroaniline, 3-fluoroaniline and 4-fluoroaniline was carried out inaqueous medium using an acidified mixture of potassium bromate andpotassium bromide as a source of bromine. The chlorination of thesecompounds was carried out using sulphuryl chloride as a chlorinatingagent in chloroform or diethyl ether. Anhydrous aluminium chloridewas used as a catalyst in the chlorination of the fluoroanilines. All the reaction products obtained were analyzed by fluorine-19 nuclear magnetic resonance spectroscopy (F n.m.r. spectroscopy), gas liquid chromatography (GLC) and high-performance liquid chromatography (HPLC).The identification and the structure of these products were established by comparison with the authentic compounds. For the thermodynamic studies:-(a) The enthalpies of solution (at saturation) of 2,4,6-tribromophenol (Br3C6H2OH), 4-bromoani1ine (BrC6H4NH2), 2,6-dibromoaniline (Br2C6H3NH2) and 2,4,6-tribromoaniline (Br3C6H2NH2) in toluene and n-propanol were determined from solubility measurements. ASO1H (Br3C6H2OH) in Toluene = 33.90 kJ mol -1Aso/ (Br3C6H2OH) in n-Propanol = 24.01 kJ mol-1AS0/ (BrC6H4NH2) in Toluene = 65.94 kJ mol -1Aso1H° (BrC6H4NH2) in n-Propanol = 61.95 kJ mol -1A SO1 H0 (Br2C6H3NH2) in Toluene = 46.65 kJ mol -1 sol ' 2 6 3 2'2AgQ-jH"0 (Br2C6H3NH2) in n-Propanol = 44.93 kj mol -1Aso1H° (Br3C6H2NH2) in Toluene = 28.09 kj mol -1Aso1H° (Br3C6H2NH2) in n-Propanol = 20.22 kJ mol -1Entropies of solution, enthalpies of transfer, free energies of transfer and the entropies of transfer between the two solvents were also calculated. (b) Enthalpies of reaction of the bromination of 2-chloroaniline, 4-bromo-2-chloroaniline and 4-chloroaniline in aqueous medium (perchloric acid/sodium bromide) with aqueous bromine (sodium bromide/sodium bromate) were found using reaction calorimetry. arH0θ (2-chloroaniline. + bromine. aq) = -207.84 - 0.63 kj mol-1r aqArH° (4-bromo-2-chloroaniline,c + bromine,aq ) = -91.29 - 0.96 kJ mol -1 ArH° (4-chloroaniline,c + bromine, aq) = -189.61 - 0.90 kJ mol-1.(c) A titration calorimetric technique was used to determine the enthalpies of bromination of 2-nitroaniline and 4-nitroanle in aqueous medium (perchloric acid/sodium bromide) with aqueous bromine (sodium bromide/sodium bromate).547Organic ChemistryRoyal Holloway, University of Londonhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.704374http://repository.royalholloway.ac.uk/items/6eed7444-a22e-47ac-bcc7-850e50d14fbb/1/Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 547
Organic Chemistry
spellingShingle 547
Organic Chemistry
Mohran, Hossnia Saber
Analytical and thermodynamic studies on some halogenated benzenoid compounds
description The bromination of 2-fluorophenol, 3-fluorophenol, 4-fluorophenol, 2-fluoroaniline, 3-fluoroaniline and 4-fluoroaniline was carried out inaqueous medium using an acidified mixture of potassium bromate andpotassium bromide as a source of bromine. The chlorination of thesecompounds was carried out using sulphuryl chloride as a chlorinatingagent in chloroform or diethyl ether. Anhydrous aluminium chloridewas used as a catalyst in the chlorination of the fluoroanilines. All the reaction products obtained were analyzed by fluorine-19 nuclear magnetic resonance spectroscopy (F n.m.r. spectroscopy), gas liquid chromatography (GLC) and high-performance liquid chromatography (HPLC).The identification and the structure of these products were established by comparison with the authentic compounds. For the thermodynamic studies:-(a) The enthalpies of solution (at saturation) of 2,4,6-tribromophenol (Br3C6H2OH), 4-bromoani1ine (BrC6H4NH2), 2,6-dibromoaniline (Br2C6H3NH2) and 2,4,6-tribromoaniline (Br3C6H2NH2) in toluene and n-propanol were determined from solubility measurements. ASO1H (Br3C6H2OH) in Toluene = 33.90 kJ mol -1Aso/ (Br3C6H2OH) in n-Propanol = 24.01 kJ mol-1AS0/ (BrC6H4NH2) in Toluene = 65.94 kJ mol -1Aso1H° (BrC6H4NH2) in n-Propanol = 61.95 kJ mol -1A SO1 H0 (Br2C6H3NH2) in Toluene = 46.65 kJ mol -1 sol ' 2 6 3 2'2AgQ-jH"0 (Br2C6H3NH2) in n-Propanol = 44.93 kj mol -1Aso1H° (Br3C6H2NH2) in Toluene = 28.09 kj mol -1Aso1H° (Br3C6H2NH2) in n-Propanol = 20.22 kJ mol -1Entropies of solution, enthalpies of transfer, free energies of transfer and the entropies of transfer between the two solvents were also calculated. (b) Enthalpies of reaction of the bromination of 2-chloroaniline, 4-bromo-2-chloroaniline and 4-chloroaniline in aqueous medium (perchloric acid/sodium bromide) with aqueous bromine (sodium bromide/sodium bromate) were found using reaction calorimetry. arH0θ (2-chloroaniline. + bromine. aq) = -207.84 - 0.63 kj mol-1r aqArH° (4-bromo-2-chloroaniline,c + bromine,aq ) = -91.29 - 0.96 kJ mol -1 ArH° (4-chloroaniline,c + bromine, aq) = -189.61 - 0.90 kJ mol-1.(c) A titration calorimetric technique was used to determine the enthalpies of bromination of 2-nitroaniline and 4-nitroanle in aqueous medium (perchloric acid/sodium bromide) with aqueous bromine (sodium bromide/sodium bromate).
author Mohran, Hossnia Saber
author_facet Mohran, Hossnia Saber
author_sort Mohran, Hossnia Saber
title Analytical and thermodynamic studies on some halogenated benzenoid compounds
title_short Analytical and thermodynamic studies on some halogenated benzenoid compounds
title_full Analytical and thermodynamic studies on some halogenated benzenoid compounds
title_fullStr Analytical and thermodynamic studies on some halogenated benzenoid compounds
title_full_unstemmed Analytical and thermodynamic studies on some halogenated benzenoid compounds
title_sort analytical and thermodynamic studies on some halogenated benzenoid compounds
publisher Royal Holloway, University of London
publishDate 1986
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.704374
work_keys_str_mv AT mohranhossniasaber analyticalandthermodynamicstudiesonsomehalogenatedbenzenoidcompounds
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