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W hen we discussed elimination reactions in Chapter 5, we learned that Lewis base can react with an alkyl halide to form an alkene. In the present chapter, you will find that the same kinds of reactants can also undergo a different reaction, one in which the Lewis base acts as a nucleophile to substitute for the halide substituent on carbon
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ot all the properties of alkenes are revealed by focusing exclusively on the func- tional group behavior of the double bond. A double bond can affect the proper- ties of a second functional unit to which it is directly attached. It can be a sub- stituent, for example, on a positively charged carbon in an allylic carbocation, or on a carbon that bears an unpaired electron in an allylic free radical, or it can
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Introduction Some questions you concern: 1 Why should we study English? 2 Why we study physics in English? 3 How about the achievement in final exam? 4 Is it helpful for your future career to study physics in English?
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the preceding chapter you learned that nucleophilic addition to the carbonyl group is one of the fundamental reaction types of organic chemistry. In addition to its own reactivity, a carbonyl group can affect the chemical properties of aldehydes and ketones in other ways. Aldehydes and ketones are in equilibrium with their enol isomers
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Example: In 1 liter pure water add 0.01 mol of hydrochloric acid. Calculate this solution's ph change value. And in 1 liter contain 0.1 mol acetic acid and 0. acetate ion mixture solution add 0.01mol of hydrochloric acid. Calculate this solution ph change value. Notice: Square bracket will instead of equilibrium concentration in following time. Such as [H+] instead hydrogen ion equilibrium concentration
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he value of alkyl halides as starting materials for the preparation of variety of organic functional groups has been stressed many times. In our earlier discussions, we noted that aryl halides are normally much less reactive than alkyl halides in reactions that involve carbon-halogen bond cleavage. In the present chapter you will see that aryl halides can exhibit their own patterns of chemical reactivity, and that these reac
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Nash equilibrium has undoubtedly proved to be the most influential idea in game theory. enabled fundamental breakthroughs in economics and the social sciences. Its development was a major intellectual achievement; what is perhaps more important, it Recent foundational research has emphasized the subtleties in the interpretation of Nash equilibrium. This lecture deals with the technical details of equilibrium analysis, but also with these interpretational issues. However, a more precise appraisal of the situation must
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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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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
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The triacylglycerol shown in text Figure 26.2a, with an oleyl group at C-2 of the glycerol unit and two ste earyl groups at C-I and C-3, yields stearic and oleic acids in a 2 I molar ratio on hydrolysis. A constitutionally isomeric structure in which the oleyl group is attached to C-1 of glycerol would yield the same hydrolysis products
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