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Groups, estimation

AppHcation groups Estimated CH2CI2 consumed, lOM Eraction, %... [Pg.553]

Event Group Estimated Mean Estimated Standard Deviation... [Pg.241]

Fudge factors built into internal support group estimates. [Pg.826]

The procedure is first to group estimations that proved to be satisfactory, then group ... [Pg.40]

Figure 3. Dependence of product yields from Mylar on dose (2). Carboxyl groups estimated by titration (PohFs method) (13)... Figure 3. Dependence of product yields from Mylar on dose (2). Carboxyl groups estimated by titration (PohFs method) (13)...
The sweetest derivative included in Eq. 51 is L-aspartylaminomalonic acid methyl fencyl ester (32) which is 63000 times as sweet as sucrose59). This is understandable on the basis of the high coefficient of the a term of Eq. 51, a high a value itself of the N-substituent containing two ester carbonyl groups (estimated as 1.38) and the (W,)2 term due to the presence of methyl groups on the R2 cyclohexyl moiety. [Pg.148]

For methoxyl and ethoxyl group estimations (p. 479) hydriodic acid (B.P. 127°) is distilled over phosphorus in a current of carbon dioxide. [Pg.506]

FIG. 6.2 Glass transition temperature of poly(methyl methacrylate) with paraffinic side groups. Estimated values Eqs. (6.6)—(6.8) Experimental values. [Pg.138]

Group estimation methods to estimate water solubility of organic chemicals"... [Pg.45]

Eventually, this should make producing a new drug a lot faster and more efficient. All told. The Boston Consulting Group estimated that the new technology s greater produc-... [Pg.73]

Solvent-exposed groups estimated by A-spectral response to co-solutesof higher refractive index AA maximum near 2350 A on change of chromophore environment... [Pg.349]

Compound X Cis group Bond length (A) Trans group Estimated standard Bond length deviation (A) (e.s.d.) Ref. [Pg.382]

The mesomeric constants, CTr, for pyrimidinyl groups estimated according to Eq. (13) proved to be practically independent of solvent polarity (78KGS996). [Pg.16]

NMR distinguishes these. The end CH2 is attached either to the nitrogen atom aiKTiated 3.2 p.p.m.) or to the carbonyl group (estimated 2.2 p.p.m.) of the amide. The jcMcrved value of 3.92 p.p.m. fits the first better. A similar estimate for the CH also suggests the i - structure. This is indeed the correct answer. [Pg.113]


See other pages where Groups, estimation is mentioned: [Pg.350]    [Pg.769]    [Pg.365]    [Pg.21]    [Pg.352]    [Pg.279]    [Pg.211]    [Pg.269]    [Pg.479]    [Pg.481]    [Pg.483]    [Pg.84]    [Pg.481]    [Pg.52]    [Pg.448]    [Pg.277]    [Pg.17]    [Pg.249]    [Pg.444]    [Pg.177]    [Pg.5]    [Pg.24]    [Pg.249]    [Pg.249]    [Pg.251]   


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Acetyl groups, estimation

Amino-groups, estimation

Carboxyl groups estimation

Electronegativities, group, estimated

Estimating thermochemical properties using group additivity

Estimation from structural group contributions

Estimation from structural group contributions systems

Estimation of Methoxyl or Ethoxyl Groups

Estimation of Phenolic Hydroxyl Groups

Estimation of acetyl groups

Estimation of acetyl groups bomb method

Estimation of acetyl groups semi-micro

Group Values and Nonlinear Correction Terms for Estimation of Solid Heat Capacity with the Goodman et al ethod

Group Values for Estimating Heats of Formation

Hydroxyl groups, estimation

Knotts Group Contributions for the Parachor in Estimating Surface Tension

Methoxyl groups, estimation

Physical properties, estimation methods group contributions

Properties group-method estimate

Property estimation methods group contribution models

Thermochemical data, estimation group additivity

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