什么是生物材料? 根据本课程的教材，目前较为合适的定义为：“用于医用器械、与生物体相互作用的无 生命性材料。”*

ow that we've reviewed the various bonding models, we are ready to examine organic compounds in respect to their structure, reactions, properties, and appli cations. Were we to list the physical and chemical properties of each of the more than million organic compounds separately, it would tax the capacity of even a pow- erful computer. Yet someone who is trained in organic chemistry can simply look at the structure

一、目标:介绍GPS卫星测量基本原理及其应用 二、PPT课件采用中英文结合方式 三、在学习制定教材的基础上,依据学生的兴趣和个人能力,学习内容和形式多样

first three chapters established some fundamental principles concerning the structure of organic molecules. In this chapter we begin our discussion of organic chemical reactions by directing attention to alcohols and alkyl halides. These two rank among the most useful classes of organic compounds because they often serve as starting materials for the preparation of numerous other families

drogen peroxide is formed in the cells of plants and animals but is toxic to them. neemen Consequently, living systems hav developed mechanisms to rid themselves of hydrogen peroxide, usually by enzyme-catalyzed reduction to water. An under- standing of how reactions take place, be they reactions in living systems or reactions in

Ikenes are hydrocarbons that contain a carbon-carbon double bond. A car- bon-carbon double bond is both an important structural unit and an important functional group in organic chemistry. The shape of an organic molecule is influ- enced by the presence of this bond, and the double bond is the site of most of the chem- ical reactions that alkenes undergo. Some representative alkenes include isobutylene(an industrial chemical), a-pinene (a fragrant liquid obtained from pine trees), and farnesene (a naturally occurring alkene with three double bonds

he Greek word stereos means\solid, \and stereochemistry refers to chemistry in three dimensions. The foundations of organic stereochemistry were laid by Jacobus van't Hoff* and Joseph Achille Le Bel in 1874. Independently of each other, van't Hoff and Le Bel proposed that the four bonds to carbon were directed toward the cor- ners of a tetrahedron. One consequence of a tetrahedral arrangement of bonds to carbon

H ydrocarbons that contain carbon-carbon triple bond are called alkynes. Non- cyclic alkynes have the molecular formula C, H2n-2. Acetylene (HCCH) is th simplest alkyne. We call compounds that have their triple bond at the end of a carbon chain(RC=CH) monosubstituted, or terminal, alkynes. Disubstituted alkynes (RCCR') are said to have internal triple bonds. You will see in this chapter that a car- bon-carbon triple bond is a functional group, reacting with many of the same reagents

rganometallic compounds are compounds that have a carbon-metal bond; they lie at the place where organic and inorganic chemistry meet. You are already familiar with at least one organometallic compound, sodium acetylide (NaC=CH), which has an ionic bond between carbon and sodium. But just because a compound contains both a metal and carbon isn't enough to classify it as organometal-

ntil the second half of the twentieth century, the structure of a substance-a newly discovered natural product, for example-was determined using information obtained from chemical reactions. This information included the identification of functional groups by chemical tests, along with the results of experiments in which the substance was broken down into smaller, more readily identifiable fragments. Typical of this approach is the demonstration of the presence of a double bond in an alkene by cat- nd subsequent