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Group Tables

There is a great deal of material on group theory of both the single and double groups. The most complete is the treatise by Altmann and Herzig (1994). In this appendix, we present information on the basis functions and principles for determining the products of basis functions. Most of this information is available elsewhere, but for convenience we present a summary here. [Pg.479]


As an example we consider the group introduced in (equation Al.4,19) and the point group given in (equation Al.4.22). Inspection shows that the multiplication table of in table Al.4,2 can be obtained from the multiplication table of the group (table Al.4,1) by the following mapping ... [Pg.148]

Band 1, 3 OSyL (3242 cm.". ) Hydrogen bonded 0—H absorption of the phenolic group (Table II). [Pg.1140]

Table ITI-100 2,4-Diarylthiazoles with substituents on the aryl groups Table III-lOl 2,5-Diarylthiazoles with substituents on the aryl groups Table 111-102 4,5-Diarylthiazoles with substituents on the aryl groups... Table ITI-100 2,4-Diarylthiazoles with substituents on the aryl groups Table III-lOl 2,5-Diarylthiazoles with substituents on the aryl groups Table 111-102 4,5-Diarylthiazoles with substituents on the aryl groups...
Table 111-103 2-Alkylthiazoles with one function on the alkyl group Table 111-104 4-Alkylthiazoles with one function on the alkyl group Table I1I-105 5-Alkylthiazoles with one function on the alkyl group... Table 111-103 2-Alkylthiazoles with one function on the alkyl group Table 111-104 4-Alkylthiazoles with one function on the alkyl group Table I1I-105 5-Alkylthiazoles with one function on the alkyl group...
Table III-IO6 Thiazoles substituted by one polyfunctional group Table III-107 Thiazoles substituted by several polyfunctional groups... Table III-IO6 Thiazoles substituted by one polyfunctional group Table III-107 Thiazoles substituted by several polyfunctional groups...
The vibrations of acetylene provide an example of the so-called mutual exclusion mle. The mle states that, for a molecule with a centre of inversion, the fundamentals which are active in the Raman spectmm (g vibrations) are inactive in the infrared spectmm whereas those active in the infrared spectmm u vibrations) are inactive in the Raman spectmm that is, the two spectra are mutually exclusive. Flowever, there are some vibrations which are forbidden in both spectra, such as the torsional vibration of ethylene shown in Figure 6.23 in the >2 point group (Table A.32 in Appendix A) is the species of neither a translation nor a component of the polarizability. [Pg.173]

As we proceed to molecules of higher symmetry the vibrational selection rules become more restrictive. A glance at the character table for the point group (Table A.41 in Appendix A) together with Equation (6.56) shows that, for regular tetrahedral molecules such as CH4, the only type of allowed infrared vibrational transition is... [Pg.180]

For a spherical rotor belonging to the octahedral Of, point group, Table A.43 in Appendix A, in conjunction with the vibrational selection rules of Equation (6.56), show that the only allowed transitions are... [Pg.181]

Because of the pyramidal shape in these excited states the orbitals and states may be reclassified according to the Q point group (Table A. 1 in Appendix A). [Pg.266]

Table no. Point group Table no. Point group Table no. Point group... [Pg.407]

The PMBs, when treated with electrophilic reagents, show much higher reaction rates than the five lower molecular weight homologues (benzene, toluene, (9-, m- and -xylene), because the benzene nucleus is highly activated by the attached methyl groups (Table 2). The PMBs have reaction rates for electrophilic substitution ranging from 7.6 times faster (sulfonylation of durene) to ca 607,000 times faster (nuclear chlorination of durene) than benzene. With rare exception, the PMBs react faster than toluene and the three isomeric dimethylbenzenes (xylenes). [Pg.504]

Monoa.lka.nola.mine Condensates. Coco, lauric, oleic, and stearic monoethanolamides and monoisopropanolamides are the principal surfactants ia the monoalkano1 amide group (Table 24). Monoalkanolamides are generally water-iasoluble soHds that are easily solubilized by hydrophilic surfactants. Except for solubiUty and viscosity, properties and uses are similar to the diethanolamides. Manufacturing processes and yields have been described (96). [Pg.253]

Melting points, boiling points, densities, and refractive indexes for carboxyUc acids vary widely depending on molecular weight, stmcture, and the presence of unsaturation or other functional groups (Tables 1,2,3, and 5). In addition, some useful constants for alkanoic acids are Hsted in Table 1. Some constants for selected unsaturated and substituted acids are given in Table 7. [Pg.82]

Resins for advanced composites can be classified according to their chemistry typical resins are polyaryletherketones, polysulfides, polysulfones, and a very broad class of polyimides containing one or more additional functional groups (Table 2) (see also Engineering plastics). [Pg.37]

The carrier-active chemical is selected according to its effectiveness at various temperatures. Members of the phenoHc group (Table 2), considered to be stronger carriers, are employed for formulations to be used in open equipment at the boil. Weaker carriers, such as the members of the aromatic ester group, are utilized generally for high temperature dyeing. [Pg.266]

Neutral azoles are readily C-lithiated by K-butyllithium provided they do not contain a free NH group (Table 6). Derivatives with two heteroatoms in the 1,3-orientation undergo lithiation preferentially at the 2-position other compounds are lithiated at the 5-position. Attempted metallation of isoxazoles usually causes ring opening via proton loss at the 3-or 5-position (Section 4.02.2.1.7.5) however, if both of these positions are substituted, normal lithiation occurs at the 4-position (Scheme 21). [Pg.69]

For purposes of data correlation, model studies, and scale-up, it is useful to arrange variables into dimensionless groups. Table 6-7 lists many of the dimensionless groups commonly founa in fluid mechanics problems, along with their physical interpretations and areas of application. More extensive tabulations may oe found in Catchpole and Fulford (Ind. Eng. Chem., 58[3], 46-60 [1966]) and Fulford and Catchpole (Ind. Eng. Chem., 60[3], 71-78 [1968]). [Pg.674]

More sophisticated GC columns and techniques perform more detailed separations of mixtures of hydrocarbons into discrete groups. Table 12-3... [Pg.202]

Because nitration has been studied for a wide variety of aromatic compounds, it is a useful reaction with which to illustrate the directing effect of substituent groups. Table 10.3 presents some of the data. A variety of reaction conditions are represented, so direct comparison is not always valid, but the trends are nevertheless clear. It is important to remember that other electrophiles, while following the same qualitative trends, show large quantitative differences in position selectivity. [Pg.562]

Dimensionless groups for a proeess model ean be easily obtained by inspeetion from Table 13-2. Eaeh of the three transport balanees is shown (in veetor/tensor notation) term-by-term under the deseription of the physieal meanings of the respeetive terms. The table shows how various well-known dimensionless groups are derived and gives the physieal interpretation of the various groups. Table 13-3 gives the symbols of the dimensions of the terms in Table 13-2. [Pg.1040]

According to Wieland, the typical lobelia alkaloids so far isolated and examined belong to three groups (Table A), all of which can be represented by the general Formula I. [Pg.23]

There are numerous families of organic compounds, with structures analogous to hydrocarbons, that contain other atoms (e.g., O, N, S, Cl) besides C and H. Classification is done in accordance with the structural theory on the basis of functional groups present. The atom or atomic grouping that characterizes a particular family and also determines the properties of its members is called a Junctional group. Table 2-42 contains a selected list of common functional groups and examples of... [Pg.312]


See other pages where Group Tables is mentioned: [Pg.1057]    [Pg.48]    [Pg.1327]    [Pg.238]    [Pg.265]    [Pg.412]    [Pg.159]    [Pg.152]    [Pg.114]    [Pg.356]    [Pg.342]    [Pg.41]    [Pg.21]    [Pg.227]    [Pg.423]    [Pg.1013]    [Pg.1327]    [Pg.980]    [Pg.284]    [Pg.359]    [Pg.360]    [Pg.270]    [Pg.582]   


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Acyl groups, table of names

Acylamino group, 131 (Table

Alcohols Compounds with a hydroxyl group Table

Alkyl group table

Alkyl groups: group frequencies correlation table

Amide functional group, 787 table

Amino functional group, 787 table

Amino group, 738 table

Biological elements, table Group

Butyl group, 702 table

C2v point group character table for

Carboalkoxy group, 131 (Table

Carbonyl group, 738 table

Carboxyl group, 738 table

Character Tables for Selected Point Groups

Character table point-group

Character tables for point groups

Character tables of point groups

Diffraction group table

Dimensionless groups table

Ether functional group, 787 table

Ethyl group, 702 table

Functional groups 2, 4, Table

Functional groups, classification table

Glycosyltransferase catalytic groups, table

Group 15 elements table

Group Correlation Tables

Group Theoretical Charts and Tables

Group character table for

Group character tables

Group multiplication table

Group names periodic table

Group numbers, periodic table references

Group properties table

Group theory character tables

Grouping Elements in the Periodic Table

Groups , and character tables

Groups , periodic table trends

Groups multiplication tables for

Groups of periodic table

Groups of the periodic table

Groups, in periodic table

Groups, in the periodic table

Groups, periodic table

Halo group, 131 (Table

Halogen functional group, 787 table

Inductive effect from functional groups, Table

Isopropyl group, 702 table

Leaving group ability, table

Leaving groups table

Methyl group, 702 table

Nitrogen functional groups containing, 31 (Table

Noble gas A Group 8 element in periodic table

Noble gases (Group 185 table

Ortho para directing groups 495 table

Periodic Table Group VIIA

Periodic Table Group VIII

Periodic Table Group numbering

Periodic Table trends down Groups

Periodic table Group 1A elements

Periodic table Group 2A elements

Periodic table Group 3A elements

Periodic table Group 4A elements

Periodic table Group 5A elements

Periodic table Group 6A elements

Periodic table Group 7A elements

Periodic table Group 8A elements

Periodic table eight-group

Periodic table families, groups, periods

Periodic table group anomalies

Periodic table group elements

Periodic table group numbers

Periodic table group/family

Periodic table groups, significance

Periodic table main groups

Periodic table main-group elements

Periodic table of the elements group number

Periodic table of the elements groups

Periodic table of the elements within groups

Periodic table vertical groups

Point Groups and Character Tables

Point Groups and Their Character Tables

Propyl group, 702 table

Protecting group table

Protecting groups. Table Acetals

Pyruvoyl groups in enzymes table

Resonance effects from functional groups, Table

Solubility groups table

Some Common Group Tables

Space group spectrum tables

Sub-groups of the Periodic Table

Sulfur functional groups containing (table

Table of functional-group preparations for

Tables 2-336 Ambrose Group Contributions for Critical Constants

Tables of the More Common Symmetry Point Groups

Tables quaternary N groups

Trace element groupings in the periodic table

Translation group character table

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