Kinetic data are reporled for the halogenation of the first five members of the fatty acid series. The influence of substitution of electron withdrawing and electron releasing group in the methyl radical of acetic acid was studied in solution. The mechanism of the reaction has been discussed. Uber
Studies on Fatty Acid-Thionyl Chloride System – Evidence of Side Reaction and the Mechanism of Inhibition in the Acetic Acid-Thionyl Chloride Reaction
✍ Scribed by Singh, H. N.
- Publisher
- John Wiley and Sons
- Year
- 1971
- Weight
- 302 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0931-5985
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✦ Synopsis
Acetic acid thionyl chloride reaction was studied in chloro-, bromo-and nitrobenzene. The reaction seems to follow simple course in the beginning, but after some time complications occur. The percentage of hydrogen chloride in the effluent gases was determined by dissolving the gases in water and measuring chloride ion concentration using silver-silver chloride electrode. The percentage of HCl in the effluent was found to increase with increasing dipole moments of solvents. Acetic anhydride and dioxane retard the reaction. Mechanism of the retardation of reaction rate by the product and added dioxane has been discussed.
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