redistribute this material, requesters must process their own requests via the RightsLink permission Xianglin Shi, Hexi Chang, Markus Grohmann, William F. Kiesman, and Daw-Iong Albert Kwok . Abstract The synthesis of ester by refluxing carboxylic acid with an excess amount of alcohol in the presence of an acidic catalyst (e.g., HCl) is known as the Fischer–Speier esterification…

Fischer Esterification is an organic reaction which is employed to convert carboxylic acids in the presence of excess alcohol and a strong acid catalyst to give an ester as the final product. The p‐toluenesulfonic acid (TsOH) is often used when dry HCl is not available. Addition of a proton (e.g.

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Energetically, the products have nearly identical stability to the starting materials and there is no significant driving force for the reaction. Electronic Supporting Information files are available without a subscription to ACS Web Editions. Find more information about Crossref citation counts. This reaction is called esterification.

EXPERIMENT #5 Fischer Esterification Table 1.

Commonly used catalysts for a Fischer esterification include sulfuric acid, p-toluenesulfonic acid (tosylic acid), and Lewis acids. The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online.
Nicholas M. Thomson, Kevin D. Seibert, Srinivas Tummala, Shailendra Bordawekar, William F. Kiesman, Erwin A. Irdam, Brian Phenix, and Daniel Kumke . Get article recommendations from ACS based on references in your Mendeley library. These metrics are regularly updated to reflect usage leading up to the last few days. without permission from the American Chemical Society. The kinetic rate constants for DMS and MMS were determined at 65 °C by fitting time-dependent experimental data to a model using DynoChem. The kinetic rate constants for DMS and MMS were determined at 65 °C by fitting time-dependent experimental data to a model using DynoChem.
the Altmetric Attention Score and how the score is calculated. not otherwise permitted to reproduce, republish, redistribute, or sell any Supporting Information If you do not receive an email within 10 minutes, your email address may not be registered, The formation and fate of monomethyl sulfate (MMS) and dimethyl sulfate (DMS) were studied by proton NMR for a sulfuric acid catalyzed esterification reaction in methanol. This material is available free of charge via the Internet at

7 publications. Vapour- and solvent-mediated crystalline transformations in Mo( Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals.

You’ve supercharged your research process with ACS and Mendeley! The mechanism of Fischer Esterification is an example of nucleophilic addition-elimination and the overall result of it is the replacement of the OH group by the OR. The synthesis of ester by refluxing carboxylic acid with an excess amount of alcohol in the presence of an acidic catalyst (e.g., HCl) is known as the Fischer–Speier esterification.

The azeotropic refluxing and acidic catalyst are found to facilitate the reaction, often by passing dry HCl gas into the solution. system.

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