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Carbon-hydrogen bonds halogenation

The carbon-halogen bonds of aryl halides are both shorter and stronger than the carbon-halogen bonds of alkyl halides In this respect as well as m their chemical behavior they resemble vinyl halides more than alkyl halides A hybridization effect seems to be responsible because as the data m Table 23 1 indicate similar patterns are seen for both carbon-hydrogen bonds and carbon-halogen bonds An increase m s... [Pg.971]

Halogen dealkylation mimics O-dealkylation both in terms of mechanism and the commonality of the process. Virtually any drug that contains a carbon-hydrogen bond adjacent to a halogen atom will be subject to P450-catalyzed oxidative dehalogenation (Fig. 4.61). [Pg.82]

FHC=CHF adlayers. Results for the Pt (100) and (111) surfaces indicated that the first step of the surface reaction is the metallation of carbon-hydrogen bonds, the activation of which is much more efficient when halogen is substituted adjacent to the carbon-hydrogen bond. [Pg.146]

Heterocumulenes undergo insertion reactions with numerous substrates. In general, carbodiimides react faster than isocyanates and isothiocyanates, in that order. Insertions of carbodiimides into metal-hydrogen, metal-halogen, metal-mitrogen, metal-oxygen and metal-sulfur bonds are reported. Also insertions of carbodiimides into carbon-hydrogen bonds are known. [Pg.78]

The overall reaction results in the reduction of carbon-halogen bonds to carbon- hydrogen bonds. [Pg.78]

To start with, we can certainly say this the carbon-hydrogen bond is stretched but not entirely broken, and the hydrogen-halogen bond has started to form but is not yet complete. This condition could be represented as... [Pg.64]

Examination of the transition state shows that this is exactly what we would expect. As we saw before (Sec. 2.22), the hydrogen-halogen bond is partly formed and the carbon-hydrogen bond is partly broken. To the extent that the bond is... [Pg.104]

All contain an acyl group, R—c- bonded to another residue. The R substituent of the acyl group may be alkyl, aryl, alkenyl, or alkynyl the other substituent to which tlie acyl fragment is bonded may be a carbon, hydrogen, oxygen, halogen, nitrogen, sulfur, or other atom. [Pg.743]


See other pages where Carbon-hydrogen bonds halogenation is mentioned: [Pg.67]    [Pg.686]    [Pg.375]    [Pg.162]    [Pg.303]    [Pg.38]    [Pg.75]    [Pg.84]    [Pg.78]    [Pg.51]    [Pg.175]    [Pg.581]    [Pg.719]    [Pg.367]    [Pg.274]    [Pg.465]    [Pg.193]    [Pg.67]    [Pg.719]    [Pg.556]    [Pg.162]    [Pg.424]    [Pg.63]    [Pg.167]    [Pg.269]    [Pg.686]   
See also in sourсe #XX -- [ Pg.552 , Pg.553 , Pg.554 ]




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Bonds carbon-halogen bond

Carbon halogenation

Carbon-halogen bonds

Carbon-hydrogen bonds

Halogen bonding

Halogen bonds/bonding

Halogens, hydrogen bonds

Hydrogen-halogen

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