Contenu d'un ouvrage

Titre de l'ouvrage : Organic Chemistry (P.Y. Bruice, 2015)

Table des chapitres

Num. Chap.	Titre du chapitre	Page
1	Remembering General Chemistry: Electronic Structure and Bonding	2
2	Acids and Bases: Central to Understanding Organic Chemistry	50
3	An Introduction to Organic Compounds: Nomenclature, Physical Properties, and Structure	88
4	Isomers: The Arrangement of Atoms in Space	143
5	Alkenes: Structure, Nomenclature, and an Introduction to Reactivity. Thermodynamics and Kinetics	190
6	The Reactions of Alkenes. The Stereochemistry of Addition Reactions	235
7	The Reactions of Alkynes. An Introduction to Multistep Synthesis	288
8	Delocalized Electrons: Their Effect on Stability, pK_A, and the Products of a Reaction. Aromaticity and Electronic Effects: An Introduction to the Reactions of Benzene	318
9	Substitution and Elimination Reactions	391
10	Reactions of Alcohols, Ethers, Epoxides, Amines, and Sulfur-Containing Compounds	458
11	Organometallic Compounds	508
12	Radicals	532
13	Mass Spectrometry; Infrared Spectroscopy; UV/Vis Spectroscopy	567
14	NMR Spectroscopy	620
15	Reactions of Carboxylic Acids and Carboxylic Acid Derivatives	686
16	Reactions of Aldehydes and Ketones. More Reactions of Carboxylic Acid Derivatives	739
17	Reactions at the α-Carbon	801
18	Reactions of Benzene and Substituted Benzenes	868
19	More About Amines. Reactions of Heterocyclic Compounds	924
20	The Organic Chemistry of Carbohydrates	950
21	Amino Acids, Peptides, and Proteins	986
22	Catalysis in Organic Reactions and in Enzymatic Reactions	1030
23	The Organic Chemistry of the Coenzymes, Compounds Derived from Vitamins	1063
24	The Organic Chemistry of the Metabolic Pathways	1099
25	The Organic Chemistry of Lipids	1127
26	The Chemistry of the Nucleic Acids	1155
27	Synthetic Polymers	1182
28	Pericyclic Reactions	1212

Chapitre 17 : Reactions at the α-Carbon	Page
The Acidity of an α-Hydrogen	802
Keto–Enol Tautomers	805
Keto–Enol Interconversion	806
Halogenation of the α-Carbon of Aldehydes and Ketones	807
Halogenation of the α-Carbon of Carboxylic Acids	809
Forming an Enolate Ion	810
Alkylating the α-Carbon	811
Alkylating and Acylating the α-Carbon Via an Enamine Intermediate	814
Alkylating the β-Carbon	815
An Aldol Addition Forms α,β-Hydroxyaldehyde or α,β-Hydroxyketone	817
The Dehydration of Aldol Addition Products Forms α,β-Unsaturated Aldehydes and Ketones	819
A Crossed Aldol Addition	821
A Claisen Condensation Forms α,β-Keto Ester	824
Other Crossed Condensations	827
Intramolecular Condensations and Intramolecular Aldol Additions	827
The Robinson Annulation	830
CO₂ Can be Removed from a Carboxylic Acid that has a Carbonyl Group at the 3-Position	831
The Malonic Ester Synthesis: A Way to Synthesize a Carboxylic Acid	833
The Acetoacetic Ester Synthesis: A Way to Synthesize a Methyl Ketone	834
Making New Carbon–Carbon Bonds	836
Reactions at the α-Carbon in Living Systems	838

Agrégation chimie Montrouge

Titre de l'ouvrage : Organic Chemistry (P.Y. Bruice, 2015)

Table des chapitres