Organic Chemistry (general higher on the chemical class of professional planning materials) and Applied Chemistry Series
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Von Händler/Antiquariat, liu xing [54261761], JiangSu, JS, China.
Ship out in 2 business day, And Fast shipping, Free Tracking number will be provided after the shipment.Pages Number: 237 Publisher: East China University of Pub. Date :2009-07-01 1 1st print version 2009-07-01 this book is based on chemistry and chemical subject teaching of the Steering Committee to develop a Undergraduate Chemistry norms elements involved in the preparation of knowledge. The book is divided into Chapter 22. including: classification and naming of organic compounds. organic compounds. the structure of the theory of weak interactions organic molecules and the physical nature of the substituent effects in organic chemistry. organic compounds. pH. carbon hydrogen bonding chemistry. organic chemistry phenomenon in the isomers. simple olefinic bond chemical bond with acetylene. conjugated olefinic bond of the chemical. aromatic chemical. carbon-halogen bond of the chemical. structural characterization of organic compounds method. Each chapter is accompanied by a number of exercises. This book can be used as an ordinary institutions of higher learning of science. engineering and medical students and other professional courses as organic materials. but also as other relevant professional readers to learn organic chemistry reference books. Contents: Chapter 1. the classification and naming of organic compounds. hydrocarbons 1.1 cycloalkanes 1.1.3 1.1.2 1.1.1 alkanes alkenes alkynes 1.1.4 1.2.1 1.1.5 halogenated aromatic hydrocarbons 1.2 1.2 General nomenclature. 2 IUPAC nomenclature 1.3 alcohol. phenol. ether. thiol ether 1.3.3 1.3.1 1.3.4 alcohol 1.3.2 phenol mercaptan 1.4 carbonyl compounds aldehydes and ketones 1.4.1 1.4.3 1.4.2 quinone carboxylic acid 1.4 .4 acid anhydride acid ester 1.4.5 1.4.7 1.4.6 acyl halides amines amide 1.5 1.5.1 1.5.2 imine nitrogen-containing organic compounds. quaternary ammonium 1.5.4 1.5.3 1.5.5 nitrile nitro compounds 1.5 .6 isonitrile and isonitrile ester diazo and azo compounds 1.5.7 Chapter 2 Exercise structural theory of organic compounds 2.2 2.1 atomic orbital theory of covalent bonds 2.2.1 Louis (Kewis) 2.3 Theory 2.2.2 Valence Bond Theory way of carbon atoms bonding hybrid orbital theory and molecular orbital theory 2.4 2.5 common organic functional groups of the frontier orbital theory. molecular orbital 2.6 2.7 2.8 principle of conservation of orbital symmetry theory of resonance structure in Chapter 3 Exercises weak interactions organic molecules with physical properties 3.1 way of molecular smell of weak interactions hydrogen bonds 3.1.1 3.2 3.1.2 van der Waals effect of weak molecular interactions hear the impact of 3.3 on the physical properties of the weak molecular interactions with the smell molecular self-assembly of hydrophobic lipophilic 3.3.1 3.3.2 the role of molecular recognition and self-assembly of the weak interaction of biological macromolecules 3.4 Exercises Chapter 4 Substituent Effects in Organic Chemistry 4.1 polar covalent bond with the inductive effect of electron delocalization 4.2 Wu conjugate effect of 4.3 over a total of conjugation induced dynamic polarization effect 4.4 4.5 4.5.1 three-dimensional effect on the three-dimensional effect of the molecular structure of its own three-dimensional effect on the molecular 4.5.2 stable 4.5.3 three-dimensional conformation of molecules reactive effect on the impact of three-dimensional 4.5.4 effect on the reaction chemistry of three-dimensional three-dimensional effect on the molecular 4.5.5 e 4.6 for the impact of space allocation substituent effect on the properties of organic compounds pH 4.6.2 4.6.1 4.6.3 stability of carbon radicals 4.6.4 carbanion stability is the stability of ionic compounds react in a way 4.6.6 4.6.5 reactivity of compounds and their product distribution 4.6.7 Spectral properties of compound exercises in Chapter 5 of organic compounds pH 5.1 Bronsted acid-base theory of acid-base 5.1.1 5.1.2 Determination of strength of the main factors affecting acid-base strength of the theory 5.

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ISBN (andere Schreibweisen): 7-5628-2549-1, 978-7-5628-2549-4