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Possible action pattern of Taka amylase, and release of tetra- and hep-tasaccharide

Possible activating interactions between ionic liquid components and reactants

Possible activation mode

Possible activation modes for the insertion of alkylidene carbenes into C-H bonds adjacent to an oxygen atom.

Possible activation profiles of an inner-sphere electron transfer, most frequently encountered, in which the electron transfer is the rate-determining step BC basic complex bj bridging complex 1 before electron transfer bj bridging complex 2 after electron transfer P products TS are transition states molar Gibbs energy .

Possible active Ru complexes in Milstein s method

Possible active site of an MCM-41-immobilized peroxotungsten species.

Possible acyclic transition-state arrangements for crotylstannane aldehyde additions leading to the syn adduct. Only one of two possible synclinal arrays is depicted.

Possible adatom

Possible adiabatic paths on a temperature-volume coordinate system.

Possible adsorbed states derived from C2CI2F4 isomers.

Possible adsorbed states of cyclopropane.

Possible adsorption mechanisms in CaA and NaX

Possible aggregated form of chiral polythiophene derivatives

Possible aggregation mechanisms for the formation of PMMA-b-Cso LCM in different solvent mixtures of ethyl acetate and decalin .

Possible aggregation mode in the micelle. Reproduced with permission from ref. 64. Copyright 2014, John Wiley and Sons.

Possible alignment of fibroin chains in silk.

Possible alignments of the magnetic field of pairs of protons

Possible alignments of two dipolar molecules that can lead to attraction and short-range structuring of hquids

Possible alignments of two dipolar molecules that can lead to attraction and short-range structuring of liquids

Possible alkylation side reactions.

Possible allocations as a function of the number of patients in each treatment group for three approaches to balancing numbers.

Possible alterations of the flatness of the pan base while heating

Possible alternative formation of cyclic rings via a carbocation

Possible alternative mechanisms involving the alkoxide as a nucleophile that could lead being incorporated in the hydrolysis product



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