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Enzymes accelerate reaction rates by lowering the activation barrier AGp. While they may undergo transient modification during the process of catalysis, enzymes emerge unchanged at the completion of the reaction. The presence of an enzyme therefore has no effect on AG for the overall reaction, which is a function solely of the initial and final states of the reactants. Equation (25) shows the relationship between the equilibrium constant for a reaction and the standard free energy change for that reaction ... [Pg.63]

Entropy changes are important in every process, but chemists are particularly interested in the effects of entropy on chemical reactions. If a reaction occurs under standard conditions, its entropy change can be calculated from absolute entropies using the same reasoning used to calculate reaction enthalpies from standard enthalpies of formation. The products of the reaction have molar entropies, and so do the reactants. The total entropy of the products is the sum of the molar entropies of the products multiplied by their stoichiometric coefficients in the balanced chemical equation. The total entropy of the reactants is a similar sum for the reactants. Equation... [Pg.999]

Assuming the reaction of black powder given in equation (2.8) is at constant pressure if only pressure-volume work is considered, the enthalpy change for the reaction at the temperature concerned is equal to the sum of the enthalpies of the products minus the sum of the enthalpies of the reactants [equation (2.17)],... [Pg.36]

Sufficient to say that, of all the members of Group 5, the analogies between phosphorus and arsenic are closest. When used as coreactant with arsenic compounds, phosphorus compounds may react interchangeably. The recent preparation of P=As compounds by Escudie et a/.22 relied on this scrambling of arsenic and phosphorus reactants (equation 8). [Pg.243]

Condensations between two three-atom fragments are surprisingly common in this field, and generally lead to thiopyran-2-ones, etc. The reader is referred to (B-79MI22504) for a tabulation of specific examples of the reaction type shown in equation (107). There are even formally three-component condensations known, though naturally they are really stepwise assemblies of the reactants (equations 108 and 109) (76JPR705,70JOC2438). [Pg.935]

The bimolecular reaction We move next to a slightly more complex case, a single step with more than one reactant (Equation 2.31). The rate equation is 2.32 if the reverse reaction may be safely omitted, these equations sim-... [Pg.92]

Micellar sodium dodecyl sulfate and polyoxyethylene(23) dodecanol, on the other hand, did not significantly affect the rate constants for nucleophilic aliphatic substitution reactions between neutral reactants (equations 39 and 40) in spite of the fact that anisylthioethane (see equation 40) is appreciably solubilized by the micelles while iodine cyanide is excluded (Herries et al., 1964). [Pg.368]

Balanced Formula units I chem.ical of reactant equation or product B... [Pg.269]

The application of transition-state theory to unimolecular reactions is very straightforward. With the subscript 1 identifying the reactant, equation (70) reduces to... [Pg.593]

For second-order kinetic processes, the limiting reactant is always the appropriate species to follow (let species denoted as A be the limiting reactant). Equations (1.5.9-1.5.11) cannot be integrated unless Cg is related to Ca- Clearly, this can be done via Equation (1.2.5) or Equation (1.2.6). Thus,... [Pg.30]

Because you want to determine AH for a reaction in which SO3 is a product rather than a reactant, Equation b must be reversed. Recall that when you reverse an equation, the sign of AH changes. The reverse of Equation b is Equation d. [Pg.507]

On the other hand, there are exceptions to the rule that a reaction must lead to three separate fragments when the potential fragments are ring members in cyclic reactants (equation S). This ty is particularly useful in synthesis. [Pg.1042]

These special cases for the surface reaction controlling the rate all follow from the form of the Langmuir isotherm. Weak adsorption corresponds to small values of 9, and Eq. (9-7) shows that 6 (or C ) is first order in (or C ), as predicted by Eq. (9-33). When the adsorption is very strong, the critical parameter is the concentration of vacant sites remaining for adsorption of reactant. Equation (9-9) shows that this is inversely proportional to the pressure of product (or C ), in agreement with Eq. (9-34). [Pg.342]

Both HjS and HjO, must be on the left because they are the reactants equation b is reversed and added to a note that the H ions cancel out. [Pg.124]

Because Pb is a reactant, equation ii has to be reversed and then added to i. This is the reaction that takes place when current is drawn from a lead-acid battery. [Pg.124]

Both react with Reactant Equation Conditions Both react with Reactant Equation Conditions Classification Both react with Reactant Equation ... [Pg.149]

In general, the reactions for polyamide formation are seldom catalyzed. The reactions to produce thermosets, such as melamine-urea or phenol-formaldehyde, require a basic or an acidic catalyst. Some polyurethane formation reactions are catalyzed by basic reactants. Equation 3.11 applies when the rate constant of the externally catalyzed reaction (k ) is much larger than that of the self-catalyzed... [Pg.46]

Intramolecular versions of vinylindole cycloaddition can occur with suitable reactants (Equation (144) and Scheme 146) <87JOC466i, 90JOC1624>. [Pg.197]


See other pages where Equation reactants is mentioned: [Pg.152]    [Pg.362]    [Pg.267]    [Pg.233]    [Pg.94]    [Pg.345]    [Pg.294]    [Pg.179]    [Pg.255]    [Pg.1521]    [Pg.409]    [Pg.62]    [Pg.62]    [Pg.236]    [Pg.619]    [Pg.133]    [Pg.306]    [Pg.243]    [Pg.349]    [Pg.179]    [Pg.255]    [Pg.21]    [Pg.619]    [Pg.130]    [Pg.231]    [Pg.133]    [Pg.362]    [Pg.990]    [Pg.66]   
See also in sourсe #XX -- [ Pg.97 , Pg.98 , Pg.99 , Pg.100 , Pg.101 ]




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