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The main menu choices may include the following: Textbook Table of Contents Start here to view chapters, main headings, or related study guide sections. To view chapter, click on chapter name. First page of chapter will appear. To view e-Text under main heading, click on chapter name, then heading name. The first page of that section will appear. To view study guide, click on heading in e-Text. Related study guide heading will appear. To return to e-Text, click on study guide heading. Textbook Website
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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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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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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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itrogen-containing compounds are essential to life. Their ultimate source is atmo- spheric nitrogen which, by a process known as nitroge. nitrogen fixation, is reduce ced to ammonia, then converted to organic nitrogen compounds. This chapter describes the chemistry of amines, organic derivatives of ammonia. Alkylamines have their nitro- gen attached to sp'-hybridized carbon; arylamines have their nitrogen attached to an sp2-hybridized carbon of a benzene or benzene-like ring
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ACYL SUBSTITUTION his chapter differs from preceding ones in that it deals with several related classes of compounds rather than just one. Included are 1. Acyl chlorides, RCCI 2. Carboxylic acid anhydrides, RCOCR 3. Esters of carboxylic acids, RCOR'99
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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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n contrast to alcohols with their rich chemical reactivity, ethers (compounds contain- ing a C-0-C unit) undergo relatively few chemical reactions. As you saw wher we discussed Grignard reagents in Chapter 14 and lithium aluminum hydride reduc- tions in Chapter 15, this lack of reactivity of ethers makes them valuable as solvents in a number of synthetically important transformatio. In the present chapter you will learn
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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-
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the preceding chapter the special stability of benzene was described, along with reac- tions in which an aromatic ring was present as a substituent. In the present chapter we move from considering the aromatic ring as a substituent to studying it as a functional
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