Publication: Kinetics and Mechanisms of Acid-Catalyzed Hydrolysis of Some N-(4 Succinimide Compounds
| dc.authorscopusid | 26040988800 | |
| dc.authorscopusid | 57659464400 | |
| dc.authorscopusid | 6701793097 | |
| dc.authorwosid | Oztürk, Seyhan/Glq-9961-2022 | |
| dc.authorwosid | Kutuk, Halil/Lif-5803-2024 | |
| dc.authorwosid | Ozturk, Seyhan/Glq-9961-2022 | |
| dc.contributor.author | Ozturk, Seyhan | |
| dc.contributor.author | Shahabi, Shahin | |
| dc.contributor.author | Kutuk, Halil | |
| dc.contributor.authorID | Oztürk, Seyhan/0000-0003-4638-5578 | |
| dc.date.accessioned | 2025-12-11T01:07:21Z | |
| dc.date.issued | 2022 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Ozturk, Seyhan; Shahabi, Shahin; Kutuk, Halil] Ondokuz Mayis Univ, Fac Arts & Sci, Chem Dept, TR-55139 Atakum, Samsun, Turkey | en_US |
| dc.description | Oztürk, Seyhan/0000-0003-4638-5578; | en_US |
| dc.description.abstract | In this study, the mechanism of acid catalyzed hydrolysis of N-(4-substitutedaryl) succinimides in different acids was investigated. These acids are hydrochloric acid, perchloric acid and sulfuric acid, which were studied at 50.0 +/- 0.1 degrees C. Analyses of the results obtained with the entropy of activation, Excess Acidity treatment and substituent effect are consistent across the entire acid studied by an A-2 mechanism. The catalytic order of strong acids for the acid catalyzed hydrolysis of the compounds studied were as HCl > H2SO4 > HClO4 in the whole range of acidity. This order is characteristics for an A-2 mechanism. | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded | |
| dc.identifier.doi | 10.52568/000998/JCSP/44.02.2022 | |
| dc.identifier.endpage | 193 | en_US |
| dc.identifier.issn | 0253-5106 | |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.scopus | 2-s2.0-85129270811 | |
| dc.identifier.scopusquality | Q3 | |
| dc.identifier.startpage | 186 | en_US |
| dc.identifier.uri | https://doi.org/10.52568/000998/JCSP/44.02.2022 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/41424 | |
| dc.identifier.volume | 44 | en_US |
| dc.identifier.wos | WOS:000787665400009 | |
| dc.identifier.wosquality | Q4 | |
| dc.language.iso | en | en_US |
| dc.publisher | Chem Soc Pakistan | en_US |
| dc.relation.ispartof | Journal of the Chemical Society of Pakistan | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Atylsuccinimides | en_US |
| dc.subject | Excess Acidity | en_US |
| dc.subject | Activation Entropy | en_US |
| dc.subject | Substituent Effect | en_US |
| dc.subject | Acid-Catalyzed Hydrolysis | en_US |
| dc.title | Kinetics and Mechanisms of Acid-Catalyzed Hydrolysis of Some N-(4 Succinimide Compounds | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
