henols are compounds that have a hydroxyl group bonded directly to benzene or benzenoid ring. The parent compound of this group, C6H,OH, called simply phe- nol, is an important industrial chemical. Many of the properties of phenols are anal- ogous to those of alcohols, but this similarity is something of an oversimplification.Like arylamine
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he major classes of organic compounds common to living systems are lipids, pro- teins, nucleic acids, and carbohydrates. Carbohydrates are very familiar to us- we call many of them\sugars.\ They make up a substantial portion of the food we eat and provide most of the energy that keeps the human engine running. Carbohy- drates are structural components of the walls of plant cells and the wood of trees. Genetic
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ipids differ from the other classes of naturally occurring biomolecules (carbohy- drates, proteins, and nucleic acids)in that they are more soluble in non-to-weakly polar solvents(diethyl ether, hexane, dichloromethathan they are in water.they include a variety of structural types, a collection of which is introduced in this chapter. In spite of the number of different structural types, lipids share a common biosyn- thetic origin in that they are ultimately derived from glucose. During one stage of car- bohydrate metabolism, called glycolysis, glucose is converted to lactic acid. Pyruvic acid is an intermediate
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he relationship between structure and function reaches its ultimate expression in the chemistry of amino acids, peptides, and protein Amino acids are carboxylic acids that contain an amine function. Under cer- tain conditions the amine group of one molecule and the carboxyl group of a second can react, uniting the two amino acids by an amide bond. Amide(peptide)bond
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PHYSICAL PROPERTIES TABLE A Selected Physical Properties of Representative Hydrocarbons Boiling Molecular Structural Melting Compound name formula point,C Alkanes Methane 182.5 Ethane CH CH3CH3
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Absolute configuration(Section 7.5): The three-dimensional Activating substituent (Sections 12.10 and 12.12): A group rrangement of atoms or groups at a stereogenic center. that when present in place of a hydrogen causes a particular Acetal(Section 17.8): Product of the reaction of an aldehyde or reaction to occur faster. Term is most often applied to a ketone with two moles of an alcohol according to the substituents that increase the rate of electrophilic aromatic
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Francis A.Carey Textbook Table of Contents Francis A. Carey Textbook Website Student Online Learning Center ORGANIC CHEMISTRY Study Guide Table of Contents Back Next
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McGraw-Hill Higher Education A Division of The McGrawp-Hill Companies ORGANIC CHEMISTRY, FOURTH EDITION Copyright 2000, 1996, 1992, 1987 by The McGraw-Hill Companies, Inc. All rights reserved. Printed in the United States of America. Except as permitted under the United States Copyright Act of 1976, no part of this publication may be reproduced or distributed in any form or by any means, or stored in a data base or retrieva
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