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Ring effect

Heats of formation can be estimated with reasonable accuracy by additivity of group increments and corrections for ring effects. [Pg.398]

Compare atomic charges and electrostatic potential maps for the three cations. For each, is the charge localized or delocalized Is it associated with an empty a-type or Tt-type orbital Examine the lowest-unoccupied molecular orbital (LUMO) of each cation. Draw all of the resonance contributors needed for a complete description of each cation. Assign the hybridization of the C" atom, and describe how each orbital on this atom is utilized (o bond, n bond, empty). How do you explain the benzene ring effects that you observe ... [Pg.97]

A modification of this method, related to the Beckmann rearrangement, entails treatment of a ketoxime with one equivalent of CDI, then four to five equivalents of a reactive halide such as allyl bromide or methyl iodide (R3X) under reflux in acetonitrile for 0.5-1.5 h. Quatemization of the imidazole ring effectively promotes the reaction by increasing the electron-withdrawing effect. The target amides then are obtained by hydrolysis. High yields, neutral conditions, and a very simple procedure make this modification of the synthesis of amides by azolides a very useful alternative. 1243... [Pg.112]

Chlorobenzene and nitrobenzene may be expected to be somewhat poorer -electron donors, but the ring effect should still be present and... [Pg.65]

This seemingly anomalous result, called the ring effect, has been investigated in more detail (20, 32). With a potential expression as simple as that for a single Lennard-Jones particle as the sorbate, it is possible to vary systematically the size (rrgucst -guest) or interaction (egues, hosi) parameters, as... [Pg.16]

The concept of the ring effect has recently been applied to the diffusion of a binary mixture of Lennard-Jones particles in zeolite NaY (57). The first particle was varied in size while the second was held fixed. The results suggest that when the diameter of the larger sorbate is close to that of the 12-ring window in zeolite NaY, the larger sorbate will diffuse faster than the smaller one. [Pg.19]

Calculation results at 177 K led to the prediction that methane diffuses from one a-cage to another at a rate of 1.9 x 1010 per sorbate per second in NaY zeolite and 24.3 x 1010 per sorbate per second in NaCaA zeolite. Thus, this is another example of a guest diffusing faster through a host with smaller pore windows (the so-called ring effect ), a phenomenon that had been observed previously only for noble gas atoms. [Pg.24]

Table VI shows that regardless of the starting isomeric olefin, selectivity is lower with Co2(CO)8 than with rhodium this is especially true when the starting isomer is conjugated. Moreover, when hydroformylation is done with Co2(CO)8, two aromatic ring effects are observed ... Table VI shows that regardless of the starting isomeric olefin, selectivity is lower with Co2(CO)8 than with rhodium this is especially true when the starting isomer is conjugated. Moreover, when hydroformylation is done with Co2(CO)8, two aromatic ring effects are observed ...
When rhodium is used, this ring effect is very important only with trans-propenylbenzene, and it becomes even more important when tri-phenylphosphine is added to rhodium. [Pg.15]

In the presence of Co2(CO)8, selectivity seems to depend on the number and relative position of the double bond substituents as well as on the reaction temperature. As is usually the case with Co2(CO)8, hydro-formylation leads mainly to the least branched aldehydes when the carbon a to the ring bears two substituents. However, when this carbon is monosubstituted, the ring effect becomes more important and CO insertion occurs on the benzylic position. [Pg.23]

The value of 10 is determined by molecular and particulate (cloud and aerosol) scattering, and surface reflection. A small fraction of the molecular scattering is the non-conservative Rotational Raman scattering (RRS) that partially fills the solar Fraunhofer lines in the scattered radiation, creating what is commonly known as the Ring effect [15] As a result, the ratio Iq/F, where F is the extraterrestrial solar flux, contains structure that is correlated with solar Fraunhofer lines. By separating these effects, one can write... [Pg.294]

Joiner, J., Bhartia, P.K., Cebu la, R.P., Hilsenrath, E McPeters, R.D., and Park, H. (1995) Rotational-Raman Scattering (Ring Effect) in Satellite Backscatter Ultraviolet Measurements, Appl. Opt., 34, pp. 4513-4525. [Pg.298]

E. B. Bagley and D. D. Christianson, Uniaxial Compression of Viscoelastic Rings - Effect of Friction at the Platen Sample Interaction for Gels and Doughs, J. Rheol., 32(6), 555-573, (1988). [Pg.307]

The basicity of these indicators can be controlled by suitable substitution of the phenyl rings effecting ionization of the corresponding benzydrols [Eq. (1.29)]. The protonation equilibria [Eq. (1.30)] is measurable by 1H or 13C NMR spectroscopy. [Pg.16]


See other pages where Ring effect is mentioned: [Pg.334]    [Pg.386]    [Pg.441]    [Pg.95]    [Pg.5]    [Pg.5]    [Pg.210]    [Pg.483]    [Pg.51]    [Pg.60]    [Pg.165]    [Pg.191]    [Pg.271]    [Pg.71]    [Pg.8]    [Pg.8]    [Pg.8]    [Pg.654]    [Pg.65]    [Pg.66]    [Pg.228]    [Pg.232]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.19]    [Pg.567]    [Pg.33]    [Pg.654]    [Pg.448]    [Pg.294]   
See also in sourсe #XX -- [ Pg.325 ]

See also in sourсe #XX -- [ Pg.16 , Pg.19 ]




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Alkenes ring size effects

Alkyl addition, aromatic ring, effect

Anomeric effect furanose rings

Anomeric equilibria ring substituent effects

Aromatic rings magnetic anisotropic effect

Aromatic rings, oxidation isotope effects

Benzene ring steric effect

Benzene ring, complexes, electronic substituent effects

Benzene rings substituents inductive effects

Carbonyl compounds ring-size effects

Catalytic ring size effect

Chelate ring size effects

Chelate rings and Jahn-Teller effect

Coffee-ring effect

Cyclic dienes effects of ring size

Cyclization reactions ring size effect

Cyclopentadienyl ligands side ring effects

Cyclopropanone, effect of ring strain reactivity

Directing Effects of Substituents in Conjugation with the Benzene Ring

Directing effects of fused benzene rings

Directing effects of the ring heteroatom

Disubstituted benzene rings directing effects

Disubstituted benzene rings steric effects

Donor Group Orientation and Chelate Ring Size Effects

Effect of Ring Substitution

Effect of aromatic rings

Effect of heterocyclic ring

Effect of ring conformation

Effect of ring size

Effect of ring size and substitution on thermodynamic polymerizability

Effect of ring substituents

Effects of Rings

Effects of a Polar Substituent and Heteroatoms in the Ring

Effects of the Thiazole Ring on Substituents

Electronic effects, epoxide ring

Epoxides, ring openings solvent effects

Esters ring size effects

Ethers ring size effects, in formation

Five-membered ring formation solvent effect

Fluorine substitution effect epoxide ring opening reaction

Isotope effects ring opening

Ketones ring size effects

Larger rings transannular effects

Magnetic field effects ring-current effect

Magnetic field effects ringing

Nucleophile effects small rings

Orientation Effects of Ring Substituents

Oxirane ring conformational effect

Part E Competing Effects Multi-substituent Rings

Radicals ring size effects

Ring Polymers Effective Isolation and Unique Properties

Ring anisotropy effects

Ring chelation effect

Ring current effect, chemical shifts

Ring current effects

Ring entropy effect

Ring opening steric effects

Ring openings solvent effects

Ring pressure effect

Ring size effect, catalytic reactions

Ring size, effect

Ring stain effect

Ring-Formation, Effect

Ring-opening polymerization effect of temperature

Ring-opening polymerization substituent effects

Ring-opening reactivity basicity effects

Ring-opening reactivity nucleophilicity effects

Rings — Transannular Effects

Rotating ring-disk method, effect

Rotational constants ring-puckering effects

SUBSTITUENT EFFECTS ON THE REACTIVITY OF BENZENE RINGS

Solvent effects oxirane rings

Solvent effects rings

Steric effect of benzene ring

Steric effect ring-opening polymerization

Steric effects rings

Substituent Effects in Substituted Aromatic Rings

Substituent Effects on the Ring-Metal Bond

Substituent effects benzene ring

Substituent effects rings

Substituent effects small rings

Substituent effects, benzene rings reactivity

Substituent effects, benzene rings reactivity ring substituents effect

Temperature effects ring opening

Temperature effects ring-opening polymerization

The Effect of Ring Size

The Ring Size Effect

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