Compounds examples

Compounds that contain both carbonyl and alcohol functional groups are often more stable as cyclic hemiacetals or cyclic acetals than as open chain compounds Examples of several of these are shown Deduce the structure of the open chain form of each... 

Cyclic Hydrocarbons with Side Chains. Hydrocarbons composed of cyclic and aliphatic chains are named in a manner that is the simplest permissible or the most appropriate for the chemical intent. Hydrocarbons containing several chains attached to one cyclic nucleus are generally named as derivatives of the cyclic compound, and compounds containing several side chains and/or cyclic radicals attached to one chain are named as derivatives of the acyclic compound. Examples are... 

Coulometry may be used for the quantitative analysis of both inorganic and organic compounds. Examples of controlled-potential and controlled-current coulometric methods are discussed in the following sections. 

The common method of naming aldehydes corresponds very closely to that of the related acids (see Carboxylic acids), in that the term aldehyde is added to the base name of the acid. For example, formaldehyde (qv) comes from formic acid, acetaldehyde (qv) from acetic acid, and butyraldehyde (qv) from butyric acid. If the compound contains more than two aldehyde groups, or is cycHc, the name is formed using carbaldehyde to indicate the functionaUty. The lUPAC system of aldehyde nomenclature drops the final e from the name of the parent acycHc hydrocarbon and adds al If two aldehyde functional groups are present, the suffix -dialis used. The prefix formjlis used with polyfunctional compounds. Examples of nomenclature types are shown in Table 1. 

Ghromium(II) Compounds. The Cr(II) salts of nonoxidizing mineral acids are prepared by the dissolution of pure electrolytic chromium metal ia a deoxygenated solution of the acid. It is also possible to prepare the simple hydrated salts by reduction of oxygen-free, aqueous Cr(III) solutions using Zn or Zn amalgam, or electrolyticaHy (2,7,12). These methods yield a solution of the blue Cr(H2 0)g cation. The isolated salts are hydrates that are isomorphous with and compounds. Examples are chromous sulfate heptahydrate [7789-05-17, CrSO 7H20, chromous chloride hexahydrate... 

Hydroxy derivatives of silanes in which the hydroxyl groups are attached to a silicon atom are named by adding the suffices -ol, -diol, -triol etc., to the name of the parent compound. Examples are ... 

Reactions in liquid ammonia (cf. Chapter 3, Section III) require a certain amount of care, since the solvent is low boiling (—33 ) and its fumes are noxious. Nevertheless, with reasonable caution, the preparation of an ammonia solution of sodium acetylide can be carried out as described. The reagent so prepared can then be directly used for displacements on alkyl halides or for additions to suitable carbonyl compounds. Examples of both reactions are given. 

When compounds contain more than one functional group in their structures, they are referred to as polyfunctional compounds. Examples include... 

Naphthenes (C Hj ) have the same formula as olefins, but their characteristics are significantly different. Unlike olefins that arc straight-chain compounds, naphthenes are paraffins that have been bent into a ring or a cyclic shape. Naphthenes, like paraffins, are saturated compounds. Examples of naphthenes are cyclopentane, cyclohexane, and methylcyclohexane (Figure 2-3). 

Knowing the formula of a compound, Fe203> you can readily calculate the mass percents of its constituent elements. It is convenient to start with one mole of compound (Example 3.4a). The formula of a compound can also be used in a straightforward way to find the mass of an element in a known mass of the compound (Example 3.4b). 

The most complex problem of this type requires you to determine the simplest formula of a compound given only the raw data obtained from its analysis. Here, an additional step is involved you have to determine the masses of the elements present in a fixed mass of the compound (Example 3.6). 

Predict the formulas of binary ionic compounds (Example C.2). 

Compare the relative lattice energies of two ionic compounds (Example 2.2). 

Two important examples of reductive metabolism of xenobiotics are the reductive dehalogenation of organohalogen compounds, and the reduction of nitroaromatic compounds. Examples of each are shown in Figure 2.13. Both types of reaction can take place in hepatic microsomal preparations at low oxygen tensions. Cytochrome P450 can catalyze both types of reduction. If a substrate is bound to P450 in the... 

How to Use the Book to Locate Examples of the Preparation of Protection of Monofunctional Compounds. Examples of the preparation of one functional group from another are found in the monofunctional index on p. x, which lists the corresponding section and page. Sections that contain examples of the reactions of a functional group are found in the horizontal rows of this index. Section 1 gives examples of the reactions of alkynes that form new alkynes Section 16 gives reactions of alkynes that form carboxylic acids and Section 31 gives reactions of alkynes that form alcohols. 

Contaminants seldom consist of single substances. The pathways used for biodegradation of some components may be incompatible with those for others that are present, or the pathway for a single compound. Examples of this are given, though in less detail than they merit. 

Temperature-Dependent Quadrupole Splitting in Paramagnetic (S = 2) Iron Compounds (Example Deoxymyoglobin)... 

Lamb-Mossbauer Factor in Spin-Crossover Compounds (Example [Fe (tpa)(NCS)2])... 

The number of known polycationic compounds of main group elements is far less than that of polyanionic compounds. Examples include the chalcogen cations S]+, S]+, Se]o and Teg that are obtained when the elements react with Lewis acids under oxidizing conditions. The ions S]1, Sc]1 and Te] have a square structure that can be assumed to have a 6n electron system. 

Substituent group Influence on membrane permeability Compound Example aa... 

The interfacial barrier theory is illustrated in Fig. 15A. Since transport does not control the dissolution rate, the solute concentration falls precipitously from the surface value, cs, to the bulk value, cb, over an infinitesimal distance. The interfacial barrier model is probably applicable when the dissolution rate is limited by a condensed film absorbed at the solid-liquid interface this gives rise to a high activation energy barrier to the surface reaction, so that kR kj. Reaction-controlled dissolution is somewhat rare for organic compounds. Examples include the dissolution of gallstones, which consist mostly of cholesterol,... 

Figure 25 shows the ternary phase diagram (solubility isotherm) for an unsolvated racemic compound. Examples of this type include benzylidenecamphor in methanol, or /V-acetylvaline in acetone [141]. In Fig. 25, A and A represent the...

R3Sb or stibonium, R4Sb+ compounds. Example for a dimetalla stibine is [PhSb(Fe(CO)2Cp)2l97 (Fig. 23a) and for trimetalla stibonium cations (type 27) [PhSb Fe(CO)2Cp 3]2[FeCl4]91. ... 

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