Title, Chimica organica. Con CD-ROM. Author, Paula Yurkanis Bruice. Edition, 2. Publisher, Edises, ISBN, , Length, Bruice – Chimica Organica. To maximize your viewing experience of this digital catalog, we recommend installing Adobe Flash Player Plugin. This installation. K. Peter, P. Vollhardt, N. E. Schore, Chimica Organica,. Zanichelli. • P. Y. Bruice, Chimica Organica, EdiSES. • T. W. Graham Solomons, Organic Chemistry.
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edise Visite Leggi Modifica Ediss wikitesto Cronologia. IV unit – Carboxylic acids and derivatives. Synthesis and retro-synthesis of molecules of low complexity Course content The concepts of chemical bonding and atom ibridization will be briefly summarized, followed by an introduction to stereochemistry and conformational analysis. Alkyl halides and alcohols reactions elimination, nucleophilic substitution, oxidation. Menu di navigazione Strumenti personali Accesso non effettuato discussioni contributi registrati entra.
Students’ evaluation View previous A. Benzene and other aromatic compounds. Planned learning activities and teaching methods: At the end of the course you will be able to draw the chemical structure of complex organic molecules, to predict their reactivity and to relate their properties with the molecular structure.
Some to choose from are listed below. Additional notes about suggested reading: Nucleophilic substitution and elimination. Schore, Chimica Organica; 4a Ed.
Textbooks and optional supplementary readings Paula Y. Give now Alma orienta Job placement. Insegnamenti online – IOL. Isomeria di posizione, edisew, conformazionale. The student has two hours at his disposal. Sostituzione nucleofila ed eliminazione. La stabilizzazione per risonanza. Vedi le condizioni d’uso per i dettagli. Programma esteso Introduzione I composti organici naturali ed i composti organici di sintesi. You will learn the main properties of the organic molecules and of biologically relevant macromolecules.
La sostituzione nucleofila aromatica.
CHIMICA ORGANICA I E LABORATORIO A – L
The prerequisites of the course are the basic principles of organic chemistry learned in the course of Organic Chemistry I. L’idroborazione di un alchino terminale edisess un’aldeide.
Show reactivity in the three dimensions. The scientific rigor of the answers, the formal correctness, the acquisition of the contents and the ability to elaborate and link them to interpret new problems or propose synthetic strategies will be evaluated.
Goals Orgamica course aims at providing the student with the knowledge required to tackle all the fundamental problems of organic chemistry, with particular emphasis focussed on the study of the chemical properties and reactivity of aliphatic compounds.
Educational offer – University of Padova
Textbooks and optional supplementary readings. Contenuti sintetici I composti organici naturali ed i composti organici di sintesi. Single cycle degree courses.
Course contents 1 Covalent bonding and shape of molecules 2 Alkanes and cycloalkanes 3 Stereochemistry and chirality 4 Acids and bases 5 Alkenes 6 Reactions of alkenes 7 Alkynes 8 Haloalkanes, halogenation and radical reactions 9 Nucleophilic substitution and beta-elimination 10 Alcohols 11 Ethers, epoxides and sulphides 12 Organometallic compounds 13 Aldehydes and ketones 14 Carboxylic acids 15 Functional derivatives of carboxylic acids 16 Enolate anions and enamines 17 Conjugated systems 18 Benzene and aromaticity 19 Reactions of benzene and its derivatives 20 Amines 21 Carbohydrates, Aminoacids and proteins.
Teaching Mode Traditional lectures. VIII unit – Laboratory experiments: Periodo di erogazione dell’insegnamento Primo semestre. Ethers, epoxides, thiols and sulphides. Teaching form Lessons, 5 credits Classes, 1 ediees. Reazioni in acidi e bruixe in basi. The student will be trained in solving simple problems of organic chemistry and retro-synthetic ediss of relatively complex structures.
Le reazioni radicaliche Il benzene e gli altri composti aromatici La stabilizzazione per risonanza. Bruiice ability to recognize the organic compounds classes alcohols, amines, aldehydes, etc. The exam is written and includes 16 theoretical questions and open-ended exercises.