The nucleophilic displacement reaction has been differentiated into SN1 and SN2 reactions. While in an SN2 reaction bond formation and breaking proceed simultaneously, the SN1 reaction proceeds via a stepwise mechanism. In most textbooks the SN1 reaction is defined as a reaction where the initial ionization (k1) is rate determining and the subsequent reaction of the carbocation with the solvent is faster. But this simple reaction scheme is only valid for systems where a highly reactive carbocation is formed. Mechanistic changes can occur when the lifetime of the intermediate carbocation is varied. The lifetime of the carbocation depends on its electrophilicity and the nucleophilicity of the solvent. The present work deals with the solvolyses of fluoro-substituted benzhydryl derivatives, the solvolyses of benzhydryl fluorides, the Change from SN1 to SN2 mechanism and the leaving group Dependence of the SN1/SN2 Ratio.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
was born in Munich, Germany, in 1980. He studied chemistry at the Ludwig-Maximilians-University in Munich and obtained his B. Sc. and M. Sc. degree. In 2007 he started his doctoral studies in the group of Professor Dr. Herbert Mayr. The present thesis represents the results of this work and led to his PhD.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The nucleophilic displacement reaction has been differentiated into SN1 and SN2 reactions. While in an SN2 reaction bond formation and breaking proceed simultaneously, the SN1 reaction proceeds via a stepwise mechanism. In most textbooks the SN1 reaction is defined as a reaction where the initial ionization (k1) is rate determining and the subsequent reaction of the carbocation with the solvent is faster. But this simple reaction scheme is only valid for systems where a highly reactive carbocation is formed. Mechanistic changes can occur when the lifetime of the intermediate carbocation is varied. The lifetime of the carbocation depends on its electrophilicity and the nucleophilicity of the solvent. The present work deals with the solvolyses of fluoro-substituted benzhydryl derivatives, the solvolyses of benzhydryl fluorides, the Change from SN1 to SN2 mechanism and the leaving group Dependence of the SN1/SN2 Ratio. 232 pp. Englisch. N° de réf. du vendeur 9783838130729
Quantité disponible : 2 disponible(s)
Vendeur : moluna, Greven, Allemagne
Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Nolte Christophwas born in Munich, Germany, in 1980. He studied chemistry at the Ludwig-Maximilians-University in Munich and obtained his B. Sc. and M. Sc. degree. In 2007 he started his doctoral studies in the group of Professor Dr. N° de réf. du vendeur 5407357
Quantité disponible : Plus de 20 disponibles
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The nucleophilic displacement reaction has been differentiated into SN1 and SN2 reactions. While in an SN2 reaction bond formation and breaking proceed simultaneously, the SN1 reaction proceeds via a stepwise mechanism. In most textbooks the SN1 reaction is defined as a reaction where the initial ionization (k1) is rate determining and the subsequent reaction of the carbocation with the solvent is faster. But this simple reaction scheme is only valid for systems where a highly reactive carbocation is formed. Mechanistic changes can occur when the lifetime of the intermediate carbocation is varied. The lifetime of the carbocation depends on its electrophilicity and the nucleophilicity of the solvent. The present work deals with the solvolyses of fluoro-substituted benzhydryl derivatives, the solvolyses of benzhydryl fluorides, the Change from SN1 to SN2 mechanism and the leaving group Dependence of the SN1/SN2 Ratio. N° de réf. du vendeur 9783838130729
Quantité disponible : 1 disponible(s)
Vendeur : preigu, Osnabrück, Allemagne
Taschenbuch. Etat : Neu. Investigations of Heterolytic Reactivity | from Fluoro-Substituted Benzhydryl Derivatives to Benzhydryl Fluorides | Christoph Nolte | Taschenbuch | 232 S. | Englisch | 2012 | Südwestdeutscher Verlag für Hochschulschriften | EAN 9783838130729 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. N° de réf. du vendeur 106649195
Quantité disponible : 5 disponible(s)
Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -The nucleophilic displacement reaction has been differentiated into SN1 and SN2 reactions. While in an SN2 reaction bond formation and breaking proceed simultaneously, the SN1 reaction proceeds via a stepwise mechanism. In most textbooks the SN1 reaction is defined as a reaction where the initial ionization (k1) is rate determining and the subsequent reaction of the carbocation with the solvent is faster. But this simple reaction scheme is only valid for systems where a highly reactive carbocation is formed. Mechanistic changes can occur when the lifetime of the intermediate carbocation is varied. The lifetime of the carbocation depends on its electrophilicity and the nucleophilicity of the solvent. The present work deals with the solvolyses of fluoro-substituted benzhydryl derivatives, the solvolyses of benzhydryl fluorides, the Change from SN1 to SN2 mechanism and the leaving group Dependence of the SN1/SN2 Ratio.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 232 pp. Englisch. N° de réf. du vendeur 9783838130729
Quantité disponible : 1 disponible(s)