Advanced organic chemistry : Part A Structure and mechanisms

Since its original appearance in 1977, Advanced Organic Chemistry has maintained its place as the premier textbook in the field, offering broad coverage of the structure, reactivity and synthesis of organic compounds. As in the earlier editions, the text contains extensive references to both the pri...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux : Carey Francis A. (Auteur), Sundberg Richard J. (Auteur)
Format : Livre
Langue : anglais
Titre complet : Advanced organic chemistry. Part A, Structure and mechanisms / Francis A. Carey and Richard J. Sundberg,...
Édition : 5th ed. 2007
Publié : Boston, MA : Springer US , [20..]
Cham : Springer Nature
Collection : Advanced Organic Chemistry
Titre de l'ensemble : Advanced Organic Chemistry
Accès en ligne : Accès Nantes Université
Accès direct soit depuis les campus via le réseau ou le wifi eduroam soit à distance avec un compte @etu.univ-nantes.fr ou @univ-nantes.fr
Note sur l'URL : Accès sur la plateforme de l'éditeur
Accès sur la plateforme Istex
Condition d'utilisation et de reproduction : Conditions particulières de réutilisation pour les bénéficiaires des licences nationales : https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017
Contenu : Chemical Bonding and Molecular Structure. Stereochemistry, Conformation, and Stereoselectivity. Structural Effects on Stability and Reactivity. Nucleophilic Substitution. Polar Addition and Elimination Reactions. Carbanions and Other Carbon Nucleophiles. Addition, Condensation and Substitution Reactions of Carbonyl Compounds. Aromaticity. Aromatic Substitution. Concerted Pericyclic Reactions. Free Radical Reactions. Photochemistry
Sujets :
Documents associés : Structure and mechanisms: Advanced organic chemistry
LEADER 06587clm a2200733 4500
001 PPN123145856
003 http://www.sudoc.fr/123145856
005 20241002160200.0
010 |a 978-0-387-44899-2 
017 7 0 |a 10.1007/978-0-387-44899-2  |2 DOI 
035 |a (OCoLC)494072997 
035 |a Springer978-0-387-44899-2 
035 |a SPRINGER_EBOOKS_LN_PLURI_10.1007/978-0-387-44899-2 
035 |a Springer-11644-978-0-387-44899-2 
100 |a 20080410f20 k y0frey0103 ba 
101 0 |a eng  |2 639-2 
102 |a US 
105 |a a a 001yy 
135 |a dr||||||||||| 
181 |6 z01  |c txt  |2 rdacontent 
181 1 |6 z01  |a i#  |b xxxe## 
182 |6 z01  |c c  |2 rdamedia 
182 1 |6 z01  |a b 
183 |6 z01  |a ceb  |2 RDAfrCarrier 
200 1 |a Advanced organic chemistry  |h Part A  |i Structure and mechanisms  |f Francis A. Carey and Richard J. Sundberg,... 
205 |a 5th ed. 2007 
214 0 |a Boston, MA  |c Springer US 
214 2 |a Cham  |c Springer Nature  |d [20..] 
225 1 |a Advanced Organic Chemistry 
320 |a Notes bibliogr. Index 
327 1 |a Chemical Bonding and Molecular Structure  |a Stereochemistry, Conformation, and Stereoselectivity  |a Structural Effects on Stability and Reactivity  |a Nucleophilic Substitution  |a Polar Addition and Elimination Reactions  |a Carbanions and Other Carbon Nucleophiles  |a Addition, Condensation and Substitution Reactions of Carbonyl Compounds  |a Aromaticity  |a Aromatic Substitution  |a Concerted Pericyclic Reactions  |a Free Radical Reactions  |a Photochemistry 
330 |a Since its original appearance in 1977, Advanced Organic Chemistry has maintained its place as the premier textbook in the field, offering broad coverage of the structure, reactivity and synthesis of organic compounds. As in the earlier editions, the text contains extensive references to both the primary and review literature and provides examples of data and reactions that illustrate and document the generalizations. While the text assumes completion of an introductory course in organic chemistry, it reviews the fundamental concepts for each topic that is discussed. The two-part fifth edition has been substantially revised and reorganized for greater clarity. Part A begins with the fundamental concepts of structure and stereochemistry, and the thermodynamic and kinetic aspects of reactivity. Major reaction types covered include nucleophilic substitution, addition reactions, carbanion and carbonyl chemistry, aromatic substitution, pericyclic reactions, radical reactions, and photochemistry. Among the changes: Coverage of the importance of computational chemistry in modern organic chemistry, including applications to many specific reactions. Expanded coverage of stereoselectivity and enantioselectivity, including discussion of several examples of enantioselective reagents and catalysts Chapter 10, Concerted Pericyclic Reactions, has been reorganized and now begins with cycloaddition reactions. The treatment of photochemical reactions has been extensively updated to reflect both experimental and computational studies of the transient intermediates involved in photochemical reactions. A companion Web site provides digital models for study of structure, reaction and selectivity. Here students can view and manipulate computational models of reaction paths. These sites also provide exercises based on detailed study of the computational models. Several chapters in Part A conclude with Topics short excursions into specific topics such as more detailed analysis of polar substituent effects, efforts to formulate substituent effects in terms of density functional theory, or the role of carbocations in petroleum refining Solutions to the chapter problems are provided to instructors online Advanced Organic Chemistry Part A provides a close look at the structural concepts and mechanistic patterns that are fundamental to organic chemistry. It relates those mechanistic patterns, including relative reactivity and stereochemistry, to underlying structural factors. Understanding these concepts and relationships will allow students to recognize the cohesive patterns of reactivity in organic chemistry. Part A: Structure and Mechanism and Part B: Reaction and Synthesis - taken together - are intended to provide the advanced undergraduate or beginning graduate student in chemistry with a foundation to comprehend and use the research literature in organic chemistry 
371 0 |a Accès en ligne pour les établissements français bénéficiaires des licences nationales 
371 0 |a Accès soumis à abonnement pour tout autre établissement 
371 1 |a Conditions particulières de réutilisation pour les bénéficiaires des licences nationales  |c https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 
410 | |t Advanced Organic Chemistry 
452 | |0 118426680  |t Advanced organic chemistry  |h Part A  |i Structure and mechanisms  |f Francis A. Carey and Richard J. Sundberg,...  |e 5th edition  |d 2007  |c New York  |n Springer  |p 1 vol. (XXI-1199 p.)  |y 978-0-387-44897-8 
606 |3 PPN027285782  |a Chimie organique  |2 rameau 
606 |3 PPN035467231  |a Réactions chimiques organiques  |x Mécanismes  |2 rameau 
606 |3 PPN027285782  |a Chimie organique  |2 rameau 
606 |3 PPN031568580  |a Réactions chimiques  |x Mécanismes  |2 rameau 
606 |3 PPN035467231  |a Réactions chimiques organiques  |x Mécanismes  |2 rameau 
610 2 |a Computer Applications in Chemistry 
610 1 |a Chemistry 
610 2 |a Organic Chemistry 
610 2 |a Physical Chemistry 
610 2 |a Medicinal Chemistry 
615 |a @Chemistry and Materials Science  |n 11644; ZDB-2-CMS  |2 Springer 
615 |a @Chemistry and Materials Science  |n 11644  |2 Springer 
676 |a 547  |v 23 
680 |a QD415-436 
700 1 |3 PPN031683223  |a Carey  |b Francis A.  |f 1937-....  |4 070 
701 1 |3 PPN031683231  |a Sundberg  |b Richard J.  |f 1938-....  |4 070 
801 3 |a FR  |b Abes  |c 20240911  |g AFNOR 
801 1 |a DE  |b Springer  |c 20200505  |g AACR2 
856 4 |q PDF  |u https://doi.org/10.1007/978-0-387-44899-2  |z Accès sur la plateforme de l'éditeur 
856 4 |u https://revue-sommaire.istex.fr/ark:/67375/8Q1-KM1T3K9P-G  |z Accès sur la plateforme Istex 
856 4 |5 441099901:830927239  |u https://budistant.univ-nantes.fr/login?url=https://doi.org/10.1007/978-0-387-44899-2 
915 |5 441099901:830927239  |b SPRING4-00092 
930 |5 441099901:830927239  |b 441099901  |j g 
979 |a NUM 
991 |5 441099901:830927239  |a Exemplaire créé en masse par ITEM le 01-10-2024 15:45 
997 |a NUM  |b SPRING4-00092  |d NUMpivo  |e EM  |s d 
998 |a 980304