Big Chemical Encyclopedia

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

Articles Figures Tables About

Rearrangement yield

Converting moles to grams and rearranging yields an equation in the form of 8.13... [Pg.255]

Replacing (ficell)s - (Tcell)x with AE and rearranging yields... [Pg.488]

Rearrangement yields a set of linear equations with two unknowns ... [Pg.244]

Assuming that a single nutrient is limiting, and eell growth is the only proeess eontributing to substrate utilization, substituting Equation 11-68 into Equation 11-66 and rearranging yields... [Pg.881]

When position 4 of perfluoropyridine is blocked with a poor leaving group, ammonia replaces the fluonne in position 2 in good yield. Oxidation of the products obtained with hypochlorite, followed by lodme-catalyzed rearrangement, yields interesting fluorodienes [78] (equation 41) Ultraviolet irradiation can be used to assist reactions m which substitution is difficult [79]... [Pg.514]

A Bi9-Catalyzed Rearrangement Yields Succinyl-CoA from L-Methylmalonyl-CoA... [Pg.792]

Integrating Equation 4-116 assuming incompressible drilling fluid flow (p is constant) and after simple rearrangements yields the pressure loss across the bit Apj (psi) which is... [Pg.839]

Once equilibrium has been reached, the rate of adsorption equals the rate of evaporation. Equating [1.1] and [1.2] and rearranging yields ... [Pg.12]

Combining Equations 4.29 and 4.30 and rearranging yield the following expression for radioligand bound in the presence of a noncompetititve antagonist ... [Pg.75]

Defining [A ]/[A] as DR (the ratio of equiactive doses) and rearranging yield... [Pg.122]

If equal responses to the agonist under these two conditions (leading to equal receptor occupancies for the same agonist, p = p ) are compared, then equating Equations 6.102 and 6.103 and rearranging yield... [Pg.125]

Subtraction of (A 1.20) from (A1.19) and rearrangement yields the same result obtained earlier ... [Pg.604]

In the rabbit, the nonplanar PCB 2,2, 5,5 -tetrachlorobiphenyl (2,2, 5,5 -TCB) is converted into the 3, 4 -epoxide by monooxygenase attack on the meta-para position, and rearrangement yields two monohydroxymetabolites with substitution in the meta and para positions (Sundstrom et al. 1976). The epoxide is also transformed into a dihydrodiol by epoxide hydrolase attack (see Chapter 2, Section 2.3.2.4). This latter conversion is inhibited by 3,3,3-trichloropropene-l,2-oxide (TCPO), thus providing strong confirmatory evidence for the formation of an unstable epoxide in the primary oxidative attack (Forgue et al. 1980). [Pg.136]

The minimal cost of equipment was used as the criterion in the design of the plant, which was to be operated in a non-overlapping mode. For a plant consisting of MB true batch units (MS = 3) and MS semi-continuous units (MS = 5) which are grouped in MST semi-continuous trains (MST = 3), the cycle time is given by Eqn. (7.4-10). Combining this expression with Eqn. (7.4-22) and rearranging yields ... [Pg.479]

Substituting the intrinsic passage into Eq. (20-58) and rearranging yields an expression for the polarization modulus c /cj, ... [Pg.39]

The expression for the activity coefficient is calculated from the differential dWei/dnk (neglecting the dependence of V on nk) by substitution into Eq. (1.3.21). Rearrangement yields... [Pg.47]

At the same time Edo has traveled a distance j = 2uf along the curve. Therefore, replacing vt by s/2 in Eq. (55) and rearranging, yields... [Pg.32]

Scheme 4-21 shows the preparation of L-threitol and L-erythritol.38 Epoxy alcohols (2J ,3iS)-61 and (2S,3/ )-61. generated by asymmetric epoxidation, are exposed to sodium benzenethiolate and sodium hydroxide in a protonic solvent to undergo base-catalyzed rearrangement, yielding the threo-diol 62 and erythro-diol 63, which can then be converted to the corresponding tetraacetate of l-threitol 67 and L-erythritol 69 through subsequent transformations. [Pg.212]

In the Briggs-Haldane derivation of the Michaelis-Menten equation, the concentration of ES is assumed to be at steady state, i.e., its rate of production [Eq. (3.12)] is exactly counterbalanced by its rate of dissociation [Eq. (3.13)]. Since the rate of formation of ES from E -(- P is vanishingly small, it is neglected. Equating the two equations and rearranging yields Eq. (3.14), where KM replaces (k2 + h)/k and is known as the Michaelis-Menten... [Pg.24]


See other pages where Rearrangement yield is mentioned: [Pg.83]    [Pg.218]    [Pg.151]    [Pg.63]    [Pg.288]    [Pg.339]    [Pg.367]    [Pg.67]    [Pg.497]    [Pg.168]    [Pg.43]    [Pg.54]    [Pg.341]    [Pg.464]    [Pg.175]    [Pg.22]    [Pg.207]    [Pg.75]    [Pg.359]    [Pg.43]    [Pg.193]    [Pg.273]    [Pg.391]    [Pg.84]    [Pg.227]    [Pg.41]    [Pg.885]   
See also in sourсe #XX -- [ Pg.50 ]

See also in sourсe #XX -- [ Pg.50 ]




SEARCH



© 2024 chempedia.info