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

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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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

1.1 The element carbon has atomic number 6, and so it has a total of six electrons. Two of these elec- tr rons are in the Is level. The four electrons in the 2s and 2p levels (the valence shell) are the valence electrons. Carbon has four valence electrons 1.2 Electron configurations of elements are derived by applying the following principles:

SOLUTIONS TO TEXT PROBLEMS 3.1 (b) The sawhorse formula contains four carbon atoms in an unbranched chain. The compound is butane, CH:CH,CH, CH3 CH3 HH H-H CH ()Rewrite the structure to show its constitution. The compound is

SOLUTIONS TO TEXT PROBLEMS 5.1 (b) Writing the structure in more detail, we see that the longest continuous chain contains four carbon atoms

SOLUTIONS TO TEXT PROBLEMS 7.1 (c)Carbon-2 is a stereogenic center in 1-bromo-2-methylbutane, as it has four different substituents: H, CH, CH,CH2, and BrCH2. H BrCH2-C-CH2CH, CH3 (d) There are no stereogenic centers in2-romo-2- me. Br CH:-C-CH,CH3 CH, 7.(b) Carbon-2 is a stereogenic center in 1, 1, 2-trimethylcyclobutane

SOLUTIONS TO TEXT PROBLEMS 9.1 The reaction is an acid-base process; water is the proton donor. Two separate proton-transfer steps are involved

assuming that there is no resonance stabilization in 1, 3,5-cycloheptatriene, we predict that its heat of hydrogenation will be three times that of cycloheptene or 330/mol (78.9 kcal/mol)