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Inactive

Borneol and isoboineol are respectively the endo and exo forms of the alcohol. Borneol can be prepared by reduction of camphor inactive borneol is also obtained by the acid hydration of pinene or camphene. Borneol has a smell like camphor. The m.p. of the optically active forms is 208-5 C but the racemic form has m.p. 210-5 C. Oxidized to camphor, dehydrated to camphene. [Pg.64]

Two molecules of vitamin A are formed from one molecule of -carotene. Vitamin A crystallizes in pale yellow needles m.p. 64 C. It is optically inactive. It is unstable in solution when heated in air, but comparatively stable without aeration. Vitamin A is manufactured by extraction from fish-liver oils and by synthesis from / -ionone. The role of vitamin A in vision seems to be different from its systemic function. See also relincne and rhodopsin. [Pg.422]

The choice of tracer gas for the measurements is Kr-85 It has a long half-life so that it can be stored for application when needed. It is a noble gas which is chemically inactive giving a low radio toxicity as it is readily removed in case of accidental contamination. [Pg.1055]

Two other examples will sufhce. Methane physisorbs on NaCl(lOO) and an early study showed that the symmetrical, IR-inactive v mode could now be observed [97]. In more recent work, polarized FTIR rehection spectroscopy was used to determine that on being adsorbed, the three-fold degeneracies of the vs and v modes were partially removed [98]. This hnding allowed consideration of possible adsorbate-adsorbent geometries one was that of a tripod with three of the methane hydrogens on the surface. The systems were at between 4 and 40 K so that the equilibrium pressure was very low, about 10 atm. [Pg.635]

Figure A2.5.30. Left-hand side Eight hypothetical phase diagrams (A through H) for ternary mixtures of d-and /-enantiomers with an optically inactive third component. Note the syimnetry about a line corresponding to a racemic mixture. Right-hand side Four T, x diagrams ((a) tlirough (d)) for pseudobinary mixtures of a racemic mixture of enantiomers with an optically inactive third component. Reproduced from [37] 1984 Phase Transitions and Critical Phenomena ed C Domb and J Lebowitz, vol 9, eh 2, Knobler C M and Scott R L Multicritical points in fluid mixtures. Experimental studies pp 213-14, (Copyright 1984) by pennission of the publisher Academic Press. Figure A2.5.30. Left-hand side Eight hypothetical phase diagrams (A through H) for ternary mixtures of d-and /-enantiomers with an optically inactive third component. Note the syimnetry about a line corresponding to a racemic mixture. Right-hand side Four T, x diagrams ((a) tlirough (d)) for pseudobinary mixtures of a racemic mixture of enantiomers with an optically inactive third component. Reproduced from [37] 1984 Phase Transitions and Critical Phenomena ed C Domb and J Lebowitz, vol 9, eh 2, Knobler C M and Scott R L Multicritical points in fluid mixtures. Experimental studies pp 213-14, (Copyright 1984) by pennission of the publisher Academic Press.
Tucceri R I and Posadas D 1990 The effect of surface charge on the surface conductance of silver in surface inactive electrolytes J. Electroanal. Chem. 283 159-66... [Pg.2756]

Michaels C A, Mullin A S, Park J, Chou J Z and Flynn G W 1998 The collisional deactivation of highly vibrationally excited pyrazine by a bath of carbon dioxide excitation of the infrared inactive (10°0), (02°0), and (02 0) bath vibrational modes J. Chem. Phys. 108 2744-55... [Pg.3015]

In practice, each CSF is a Slater determinant of molecular orbitals, which are divided into three types inactive (doubly occupied), virtual (unoccupied), and active (variable occupancy). The active orbitals are used to build up the various CSFs, and so introduce flexibility into the wave function by including configurations that can describe different situations. Approximate electronic-state wave functions are then provided by the eigenfunctions of the electronic Flamiltonian in the CSF basis. This contrasts to standard FIF theory in which only a single determinant is used, without active orbitals. The use of CSFs, gives the MCSCF wave function a structure that can be interpreted using chemical pictures of electronic configurations [229]. An interpretation in terms of valence bond sti uctures has also been developed, which is very useful for description of a chemical process (see the appendix in [230] and references cited therein). [Pg.300]

Chemically, carbon dioxide is not very reactive, and it is often used as an inactive gas to replace air when the latter might interact with a substance, for example in the preparation of chromium II) salts (p. 383). Very reactive metals, for example the alkali metals and magnesium can, however, continue to bum in carbon dioxide if heated sufficiently, for example... [Pg.182]

Initially the dataset contained 818 compounds, among which 31 were active (high TA, low USE), 157 inactive (low TA, high USE), and the rest intermediate. When the complete dataset was employed, none of the active compounds and 47 of the inactives were correctly classified by using Kohonen self-organizing maps (KSOM). [Pg.221]

Next, the technique described above (our method) was applied to the subclasses of inactive and intermediate compounds. This time 25 active compounds and 35 inactive compounds (fi om the remaining 68) were correctly classified by the same method, namely, KSOM. [Pg.221]

It is interesting to note that in a case where the same numbers of inactive and of intermediate compounds were mechanically removed (i.e., without consideration of similarity), no improvement was observed - moreover, the model quality became even worse. [Pg.221]

Ch em uses Slater atom ic orbitals to con struct sent i-em pirical molecular orbitals. I he complete set of Slater atomic orbitals is called the basis set. Core orbitals are assumed to be chemically inactive and arc not treated explicitly. Core orbitals and the atomic nucleus form the atomic core. [Pg.43]

Discriminant emalysis is a supervised learning technique which uses classified dependent data. Here, the dependent data (y values) are not on a continuous scale but are divided into distinct classes. There are often just two classes (e.g. active/inactive soluble/not soluble yes/no), but more than two is also possible (e.g. high/medium/low 1/2/3/4). The simplest situation involves two variables and two classes, and the aim is to find a straight line that best separates the data into its classes (Figure 12.37). With more than two variables, the line becomes a hyperplane in the multidimensional variable space. Discriminant analysis is characterised by a discriminant function, which in the particular case of hnear discriminant analysis (the most popular variant) is written as a linear combination of the independent variables ... [Pg.719]

Fig. 12.39 Tree describing the rules to differentiate active and inactive inotropic compounds. Each of the terminal nodes corresponds to the numbers of active and inactive molecules produced by the application of the preceding rules. Fig. 12.39 Tree describing the rules to differentiate active and inactive inotropic compounds. Each of the terminal nodes corresponds to the numbers of active and inactive molecules produced by the application of the preceding rules.
This is used extensively for qualitative analysis, for it is a rapid process and requires simple apparatus. The adsorbent is usually a layer, about 0 23 mni. thick, of silica gel or alumina, with an inactive binder, e.g. calcium sulphate, to increase the strength of the layer.. A. i i slurry of the absorbent and methanol is commonly coated on glass plates (5 20 cm. or 20 x 20 cm.), but microscope... [Pg.58]

The m.p. of the quinone obtained from the optically inactive camphor is almost identical with the above values, obtained from dextro-camphor. [Pg.148]

The activity of an enzyme varies considerably with acidity and there is generally a marked optimum pH for each enzyme. Thus pepsin of the stomach has an optimum pH of 1 4, i.e., it works best in a decidedly acid medium. It is inactive in neutral or alkaline solutions and the latter rapidly destroy it. [Pg.509]

Catalase living tissues of plants and animals hydrogen peroxide HjO and inactive molecular O, 70... [Pg.511]

Fill two burettes A and B w ith A//10 HCl. Run in from A, drop by drop, sufficient A/,To hydrochloric acid just to discharge the red colour in A. Maintain the temperature at about 60° and keep the colour just discharged by cautiously adding the HCl from time to time. Care must be taken not to add an excess of acid, otherwise the proteins will be precipitated and the enzyme rendered inactive. The reaction is o>m plete in about 5 minutes, but allow the mixture to stand for a further 5 minutes after the final discharge of the colour. [Pg.520]

The inactive aec.-octyl hydrogen phthalate may be recrystallised from light petroleum, b.p. 60-80°, or from glacial acetic acid, and then melts at 55°. [Pg.507]

The catalyst is inactive for the hydrogenation of the (isolated) benzene nucleus and so may bo used for the hydrogenation of aromatic compounds containing aldehyde, keto, carbalkoxy or amide groups to the corresponding alcohols, amines, etc., e.g., ethyl benzoate to benzyl alcohol methyl p-toluate to p-methylbenzyl alcohol ethyl cinnamate to 3 phenyl 1-propanol. [Pg.873]

Gr. argos, inactive) Its presence in air was suspected by Cavendish in 1785, discovered by Lord Rayleigh and Sir William Ramsay in 1894. [Pg.43]

Apart from Bronsted acid activation, the acetyl cation (and other acyl ions) can also be activated by Lewis acids. Although the 1 1 CH3COX-AIX3 Friedel-Crafts complex is inactive for the isomerization of alkanes, a system with two (or more) equivalents of AIX3 was fonnd by Volpin to be extremely reactive, also bringing abont other electrophilic reactions. [Pg.194]


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Achiral molecules optical inactivity

Active and Inactive Sites in COad Electro-Oxidation

Active and inactive forms

Active centre inactive

Active inactive

Active islands inactive electrodes

Active living inactivity

Active/inactive medium

Amperometric sensors for redox-inactive cations

Amperometric sensors for redox-inactive cations and electroactive compounds

Analysis of Surface-Inactive Ions

Anions surface-inactive

Aspartic proteases as inactive zymogens

Assembly inactive

Carotenoids inactive

Catalytically inactive kinase-like

Catalytically inactive kinase-like domain

Cation surface-inactive

Chemically Inactive Ionic Polymers

Chymotrypsinogen inactive precursor

Cobalt inactive

Coordinates inactive

Costs of Inaction

Distribution of inactive chains

Dosage forms inactive ingredients

Dried Inactive Yeast Powder

Drug delivery systems inactive ingredients

Elastically inactive cycles

Electro-Inactive Compounds

Electroactive-inorganic-polycrystals-based chemical for redox-inactive cations

Electrochemical inactive matrix

Electrodes inactive

Employment, unemployment and inactivity

Filler inactive”, inert

Fillers, active inactive

Fructose Inactive

Glycogen Inactive

Glycogen synthetase inactive form

Inactive Blacks

Inactive Form of an Enzyme

Inactive Ingredient Guide

Inactive SKUs

Inactive atoms

Inactive chromatin

Inactive coke

Inactive complex

Inactive compounds

Inactive corrinoid compounds

Inactive drug

Inactive energy

Inactive excitations

Inactive factor

Inactive form of the enzyme

Inactive frequency of ethylene

Inactive gases

Inactive ingredient

Inactive kinase conformations

Inactive metabolites

Inactive normal vibration

Inactive orbitals

Inactive oxidative metabolit

Inactive proteins, assay

Inactive receptor

Inactive sequences

Inactive side effects

Inactive steroids

Inactive subspaces

Inactive substituted sulfonamides

Inactive sulphur

Inactive supports

Inactivity

Inequality constraints inactive

Infrared inactive bond

Infrared-inactive

Iron derivatives, inactive

Kinase Inhibitors - Stabilizing Inactive Enzyme Conformations

Kinase inactive

Lactic acid Inactive

Limonene, inactive

Malic acid Inactive

Materials inactive

Meso Compounds Have Asymmetric Centers but Are Optically Inactive

Molecules infrared inactive

Nitrate reductase inactive

Nitration in mixtures and solutions including inactive substances

Optical inactivity

Optical inactivity, definition

Optically inactive

Optically inactive compounds

Optically inactive mixtures

Optically inactive states

Optically inactive substance

Phosphorylase inactive

Phosphorylases kinase active, inactive

Photo-inactive

Polarographically inactive

Polarographically inactive compounds

Polymer inactive

Polymerization-inactive complexes of ions

Potassium inactive form

Potential of emersed electrodes in inactive gas

Precursor inactive

Procarboxypeptidase, inactive precursor

Pyroprocess Integrated Inactive

Pyroprocess Integrated Inactive Demonstration Facility

Raman inactive

Redox inactive

Redox-inactive cations

Redox-inactive cations amperometric sensors

Remote or Inactive Positions

Screen, inactive compounds

Sensors for redox-inactive cations

Soft drug inactive metabolite

Soft drugs inactive metabolite-based

Some Vibrations Are Infrared Inactive

Stereo-chemically active versus inactive lone pairs

Stereochemically inactive electron pair

Sterically Inactive Lone Pairs

Steroids ketonic, inactive

Surface inactive components

Surface inactive electrolyte

Surface inactivity

Surfactant adsorption surface activity/inactivity

Tablet inactive ingredients

Thermal inactivity

Transformation of Inactive

Transition metal inactive

Vibration infrared inactive

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