Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Formation table

These gases have lower thermal stabilities than hydrogen sulphide as expected from their enthalpies of formation Table 10.2) and they are consequently more powerful reducing agents than hydrogen sulphide. [Pg.284]

The common name of an ester consists of two words. The first word (methyl, ethyl,...) is derived from that of the alcohol the second word (formate, acetate,...) is the name of the acid with the -ic suffix replaced by -ate. Thus ethyl formate (Table 22.4) is made from ethyl alcohol and formic acid ... [Pg.595]

Available data on mil in-house or contractor developed compns are presented below using USA mil specs as well as tabular format (Tables... [Pg.538]

A variety of such ternary catalytic systems has been developed for diastereoselective carbon-carbon bond formations (Table). A Cp-substituted vanadium catalyst is superior to the unsubstituted one,3 whereas a reduced species generated from VOCl3 and a co-reductant is an excellent catalyst for the reductive coupling of aromatic aldehydes.4 A trinuclear complex derived from Cp2TiCl2 and MgBr2 is similarly effective for /-selective pinacol coupling.5 The observed /-selectivity may be explained by minimization of steric effects through anti-orientation of the bulky substituents in the intermediate. [Pg.15]

In Chapter 10 of Part A, the mechanistic classification of 1,3-dipolar cycloadditions as concerted cycloadditions was developed. Dipolar cycloaddition reactions are useful both for syntheses of heterocyclic compounds and for carbon-carbon bond formation. Table 6.2 lists some of the types of molecules that are capable of dipolar cycloaddition. These molecules, which are called 1,3-dipoles, have it electron systems that are isoelectronic with allyl or propargyl anions, consisting of two filled and one empty orbital. Each molecule has at least one charge-separated resonance structure with opposite charges in a 1,3-relationship, and it is this structural feature that leads to the name 1,3-dipolar cycloadditions for this class of reactions.136... [Pg.526]

The methods summarized by Eqs. 8 and 9 have both been applied to halocarbenes. The proton affinities obtained by ICR bracketing125 (Table 6) are consistently lower than those derived from enthalpies of formation (Table 7). The case of dichlorocarbene, with a difference in AH of 15 kcal/mol), is particularly disturbing and has been analysed in some detail.134 Notably, the PA of CCl2 from an earlier bracketing experiment126 was closer to the enthalpy-derived PA. The discrepant results from similar experiments125126 indicate that HCClJ is not a good substrate for proton transfer studies. [Pg.38]

The addition of the second methyl group on the phenol ring led to the observation of the consecutive inclusion process with a decrease in the dynamics for complex formation (Table 8, cf. 29 with 28 (R = CH3)). This result supports the previous suggestion190 that small guests can slip into the CD cavity and in one process form the stable host-guest complex. [Pg.207]

In the reduction of C-C triple bonds with chromous sulfate in water, the key intermediate consists of a dichromium complex with the alkyne (Scheme 20.29) [119]. This configuration assures the selective formation of trans double bonds. Various substrates have been reduced in excellent yields without the occurrence of isomerizations or byproduct formation (Table 20.4). [Pg.611]

Substituted cyclopropyl ylides also participate in oxaspiropentane formation (Table 2, entries 4d, 30b, 38, and 39). Of the two cyclopropyl carbons that can move in the rearrangement to cyclobutanones, the carbon that best stabilizes a... [Pg.29]

Hazard communication to users of dangerous chemical substances and preparations is accomplished by labelling and by means of safety data sheets (SDS), which give more detailed information to industrial users. An SDS has to be provided on request to the public for non-industrial preparations. There is a standard EU 16-heading format (Table 5) specified in the SDS Directive (a. 8). [Pg.8]

Head box Fourdrinier formation table Press section... [Pg.87]

Table 55. Estimated heats of formation Table 56. The carbon-carbon double bond... Table 55. Estimated heats of formation Table 56. The carbon-carbon double bond...
Few relevant data are available. Both equilibrium and rate constants have been measured for very few reaction series in solution, but comparisons are possible for lactone and thiolactone formation, and for a few anhydrideforming reactions (Tables 4 and 5). For lactone formation (Table 4) the EM for the rate process is of the same order of magnitude as that derived from the equilibrium constant data, and in some cases actually exceeds it (though only in one case by an amount clearly greater than the estimated uncertainty which is nominally a factor of 4 for these ratios). Lactonization generally involves rate-limiting breakdown of the tetrahedral intermediate, and the transition state is expected to be late and thus close in structure to the conjugate acid of the lactone. [Pg.202]

Enthalpy of Formation. Tables of enthalpies of reaction generally list the enthalpies of formation of various compounds in their standard states from the elements in their standard states at the specified temperature. Thus, if the standard molar enthalpy of formation, Af//, of CO2 at 25°C is given as —393.509 kJ mol , the following equation is implied ... [Pg.48]

Equipment selection is important, as is also the proper operation of the contacting devices. It is generally recognized that high shear is the primary cause of droplet haze and subsequent emulsion and crud formation. Thus, the type and amount of agitation (shear) must be optimized for mass transfer while minimizing emulsion and crud formation. Table 7.5 indicates items of information that may be required in analysis of crud formation problems in a plant [32]. [Pg.324]

Rovis and Vora sought to expand the utility in alpha redox reactions to include the formation of amides [116]. While aniline was previously demonstrated as an efficient nucleophile in this reaction (Scheme 29), attempts to develop the scope to include non-aryl amines as various primary and secondary amines resulted in low yields. The discovery of a co-catalyst was the key to effecting amide formation (Table 15). Various co-catalysts, including HOBt, HOAt, DMAP, imidazole, and pentafluorophenol, are efficient and result in high yields of a variety of amides including those involving primary and secondary amines with additional functionality. [Pg.114]

Section 2 of the textbook includes chapters that are relevant to the four genres covered in section 1. In these chapters, you will learn to format tables, hgures, and schemes (chapter 16) as well as citations and references (chapter 17). In the last chapter (chapter 18), you will End useful hints for the hnal stages of revision for all your written work. [Pg.25]

Compare this table (adapted from Vesely et al., 2003) with Table 2 in excerpt 4A. Using Table 2 as a guide, identify five formatting mistakes in the table below (we found six). (See chapter 16 for more information on formatting tables.)... [Pg.117]

Table 16.2 Some generally accepted guidelines for formatting tables. (Because formatting conventions vary, consult the appropriate Information for Authors for specific guidelines.)... Table 16.2 Some generally accepted guidelines for formatting tables. (Because formatting conventions vary, consult the appropriate Information for Authors for specific guidelines.)...
Convert the following information into a properly formatted table, with an appropriate table title. Assume that you are preparing the table for an expert audience. [Pg.538]

Problem 46 Use the chart of standard free energies of formation (Table l4-6) to determine the free energy change in the following reaction and report whether the reaction will proceed. [Pg.152]

Consulting the standard enthalpies of formation (Table l4-3), what is the enthalpy change, AH, for this reaction ... [Pg.153]

A further enhanced degree of reduction leads to chains of group 14 elements with Ne values between 6 and 6.6 e/atom. These values cover the range between twofold bound silicon atoms in one-dimensionally extended zigzag chains and 2 dumbbells. Isolated chains reside in between these border structures and therefore compete with them [14]. This leads to the expectation of an extreme cation size dependence of the anion formation. Table 4 contains the reported isolated homoa-tomic chains in solid state compounds. [Pg.34]

Fig. 5.18 Heat evolution from insulated concrete cubes containing calcium chloride and formate. Table 5.1 The effect of calcium chloride and formate on mortar stiffening times... Fig. 5.18 Heat evolution from insulated concrete cubes containing calcium chloride and formate. Table 5.1 The effect of calcium chloride and formate on mortar stiffening times...

See other pages where Formation table is mentioned: [Pg.510]    [Pg.403]    [Pg.594]    [Pg.233]    [Pg.128]    [Pg.251]    [Pg.1054]    [Pg.232]    [Pg.80]    [Pg.289]    [Pg.1054]    [Pg.75]    [Pg.144]    [Pg.124]    [Pg.189]    [Pg.630]    [Pg.187]    [Pg.182]    [Pg.62]    [Pg.534]    [Pg.210]    [Pg.233]    [Pg.126]   
See also in sourсe #XX -- [ Pg.536 ]




SEARCH



Adopt a Flexible Format for Identifying Tables, Figures, and Sources

Connection Table Format description

Connection table formats

Connection table formats GEMINI

Enthalpies of formation, table

Formation reaction table

Formation, heats tables

Formatting Schemes, Tables

Heat of formation table

Intermetallic compound formation periodic table

Metal complexes formation constants, table

Periodic table ionic formation

Periodic table metal formation

Primary amines, 31 (Table formation

Tables formatting

© 2024 chempedia.info