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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Datta, Mira (nee Sarkar) | - |
| dc.contributor.author | Kundu, Kiron K | - |
| dc.date.accessioned | 2018-03-20T04:51:37Z | - |
| dc.date.available | 2018-03-20T04:51:37Z | - |
| dc.date.issued | 1993-06 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/43906 | - |
| dc.description | 478-484 | en_US |
| dc.description.abstract | Transfer free energies, G, of trimethylammonium hydrochloride (Me3NHCl)-a precursor to a potential model for the transition state (TS) for SNl-type hydrolysis of tert-butylchloride (t-BuCI), have been determined in aqueous mixtures of various organic co solvents viz protic ten-butanol (t-BuOH), ethylene glycol (EG), glycerol (GL) and methoxyethanol (ME), aprotic dimethoxyethane (DME) and dioxane (D) and dipolar aprotic 1,2-dimethylformamide (DMF) and dimethyl sulphoxide (DMSO). These have been determined by measuring the solubilities of sparingly soluble salt Me3NHBPh4 (Ph = phenyl) at 25ᵒC in the solvents and by using the relation: G (Me3NHCl) = G ( Me3NHBPh)4 - G (Ph4B-) + G (Cl-). | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.32A(06) [June 1993] | en_US |
| dc.title | Transfer free energies of trimethylammonium hydrochloride-a precursor to a potential model transition state for SNl-type hydrolysis of tert-butyl chloride in some aquo-organic solvents | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.32A(06) [June 1993] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 32A(6) 478-484.pdf | 4.9 MB | Adobe PDF | View/Open |
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G, of trimethylammonium hydrochloride (Me3NHCl)-a precursor to a potential model for the transition state (TS) for SNl-type hydrolysis of tert-butylchloride (t-BuCI), have been determined in aqueous mixtures of various organic co solvents viz protic ten-butanol (t-BuOH), ethylene glycol (EG), glycerol (GL) and methoxyethanol (ME), aprotic dimethoxyethane (DME) and dioxane (D) and dipolar aprotic 1,2-dimethylformamide (DMF) and dimethyl sulphoxide (DMSO). These have been determined by measuring the solubilities of sparingly soluble salt Me3NHBPh4 (Ph = phenyl) at 25ᵒC in the solvents and by using the relation:
(Me3NHCl) =