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K-bonding

Give explieit expressions for how the modified foree eonstant k, bond length fg, and... [Pg.365]

Insertion into the CpTi—K Bond. Sulfur dioxide yields sulfones and ultimately sulfinates. The latter are available also from RS02Na, where R is CH, C2H3,... [Pg.160]

Van Ooij, W.J. and Jayaseelan, S.K., Bonding metals to rubber using functional and nonfunctional silanes. In Adhes. 99, 7th Int. Conf. Adhes. and Adhes., Conference Prep. 1999, pp. 43-48. [Pg.708]

The C-F bonds in 1 fluoroalkenes and fluorobenzenes also are very strong (Table 17), but alkene k bond strengths vary with the level of fluonnabon (Table 18) Both CHF=CF2 and CF2=Cp2 have significantly weaker 7t bonds than CH2= CH2, CH7=CHF, and CH2=Cp2, consistent with other data indicatuig that tn- and tetrafluonnation thermodynamically destabilize double bonds [75] The low n bond energy in Cp2=CF2 underlies its propensity to undergo thermal biradical [2-1-2] cycloaddibons [103] (see p 767 )... [Pg.993]

Examine the HOMO-2 forphenylisocyanide. Is it directly involved in any o or K bonds If so, which bonds If not, describe where it is located. Draw a Lewis structure for the molecule which is consistent with your result. [Pg.43]

A simple-minded picture suggests that the CC K bonds in aUcynes and alkenes ought to be similar. Are they Consider the thermodynamics of reduction of phenylacetylene to first give styrene and then phenylethane. (The energy for H2 is given at right.)... [Pg.115]

Whereas the initial hydrogenation both breaks a K bond, as well as destroys any aromatic stabilization, the second hydrogenation only breaks the k bond. Is this difference large as in benzene (see discussion at right), or is it much smaller or neglible Is thiophene aromatic ... [Pg.215]

I We could remove the hydrogen and one electron (H-) from the C—K bond, leaving a cydopentadienyl radical. [Pg.525]

Each local metal-ligand interaction in a complex might include a contribution from K bonding. We now remove the restriction of only local <7 bonding adopted above. [Pg.114]

An interesting bicyclic germyl anion 42 K was readily prepared by the reduction of bicyclic iodide 78 with KCg (Scheme 2.71). The Ge anionic center in 42 [K (dme)2] was highly pyramidalized with the normal value of the Ge-K bond distance (3.4324(10) A). However, in polar solvents (THF) the Ge-K bond dissociates to produce 42 as an SSIP featuring the free anion 42 . [Pg.106]

K bond dissociation enthalpy, unless otherwise noted. [Pg.225]

Corresponds to the C—H bond dissociation energy in the trimethylsilyl radical, implying a K bond strength of 192-193 kJ/mol. [Pg.225]

CH3 -Zn with superstoichiometric (defect) zinc atoms (Zn -impurity centres of conductivity). The larger is the electric positivity of the metal in these complexes, the larger is the ionicity of the carbon-metal bond, carbon being at the negative end of the dipole. Thus, in the case of C - K bond, ionicity amounts to 51%, whereas for C - Mg and C - Zn bonds ionicity amounts to 35% and 18%, respectively [55]. Consequently, metalloorganic compounds are characterized by only partially covalent metal-carbon bonds (except for mercury compounds). [Pg.265]

Maximum overlap between the p orbitals of a k bond occurs when the axes of the... [Pg.39]

An addition results in the conversion of one k bond and one a bond into two a bonds ... [Pg.319]

The unpaired electron of the allyl radical and the two electrons of the k bond are delocalized over all three carbon atoms. [Pg.502]

Figure 10 Annular k bonding, transannular k -k bonding (a) and additional charge delocalization through an np2 >na interaction (b)... Figure 10 Annular k bonding, transannular k -k bonding (a) and additional charge delocalization through an np2 >na interaction (b)...
Alkenes are more reactive than alkanes because of the presence of the pi (k) bond (discussed on page 28). The k electrons in the C=C... [Pg.89]

Smith, M. K., Bond, J. Mellin, B. 1997. The Accident Database capturing corporate memory. Rugby IChemE, SHE Department. [Pg.130]

All single bonds between two atoms are sigma (o) bonds. Pi bonds can only be formed after a sigma bond has already been formed. Therefore a double bond contains one o and one n bond, and a triple bond contains one o and two k bonds. [Pg.38]

A k bond can not be formed alone. It can be formed after the formation of a o bond, if any unhybridized p-orbitals of atoms remain. In another words, to form a it bond, two atoms must form a a bond first. [Pg.39]

As a result, in the C2H2 molecule there are three o and two k bonds, so in total five bonds. [Pg.41]

Also, each 7t bond added to a a bond makes the bond shorter. So the bond length between two carbon atoms decreases as k bonds are added. [Pg.41]


See other pages where K-bonding is mentioned: [Pg.190]    [Pg.193]    [Pg.215]    [Pg.999]    [Pg.193]    [Pg.215]    [Pg.16]    [Pg.101]    [Pg.24]    [Pg.105]    [Pg.10]    [Pg.225]    [Pg.477]    [Pg.496]    [Pg.469]    [Pg.116]    [Pg.113]    [Pg.214]    [Pg.634]    [Pg.276]    [Pg.396]    [Pg.237]    [Pg.315]    [Pg.40]    [Pg.41]    [Pg.42]    [Pg.42]   
See also in sourсe #XX -- [ Pg.106 , Pg.216 ]




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