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CH2=CH ONO

OjNKelVCIXONO CH ONOs), and about 20% dmitrophenylglycol dinitrate, (02N)2C6H3.CH(0N02).CH2(0N02)... [Pg.719]

PMR studies of the corrinoids 90, 93) have shown that the t value of the proton on the methene bridge Cio depends on the nature of the axial ligands, and that there is some correlation between the t value and the energy of the first electronic transition of the corrin ring. When Y = Bz the resonance moves to higher field in the order X = HgO < HO < CH2=CH < CHs . Finally Hill et al. (91) have shown that there is a correlation between the t value of the methyl protons in [Co(DMG)2 P 3-X] and the Hammett function of X, the t values increasing in the order X = N02 < CN < Cl Br 1 ONO < alkyls. [Pg.390]

Alkanes that form rings, or cycles, are called cycloalkanes. As T Figure 24.5 illustrates, cycloalkane structures are sometimes drawn as line structures, which are polygons in which each corner represents a CH2 group. This method of representation is similar to that used for benzene rings, ono (Section 8.6) (Remember from our benzene discussion that in aromatic structures each vertex represents a CH group, not a CH2 group.)... [Pg.1049]

CisH oNO S]- f-Butyl 2-benzoylthio-l-methoxycarbonylethyl nitroxide COjCH, (CHjIjCNCHCHjSCOCsH, < ) Photochemical reaction of (QH5C0S)2 + CH2=CHC02CH3- -(CH3)3CN0/ CsH, EPR/ 295 N 1.40 H(CH) 0.26 77Sat5 74bj... [Pg.320]


See other pages where CH2=CH ONO is mentioned: [Pg.748]    [Pg.369]    [Pg.373]    [Pg.252]    [Pg.724]    [Pg.421]    [Pg.477]    [Pg.783]    [Pg.146]    [Pg.748]    [Pg.369]    [Pg.373]    [Pg.252]    [Pg.724]    [Pg.421]    [Pg.477]    [Pg.783]    [Pg.146]    [Pg.75]    [Pg.252]    [Pg.146]    [Pg.246]    [Pg.138]    [Pg.507]    [Pg.133]    [Pg.748]    [Pg.75]    [Pg.58]    [Pg.58]    [Pg.6]    [Pg.233]    [Pg.155]    [Pg.1082]    [Pg.233]    [Pg.13]    [Pg.56]    [Pg.129]    [Pg.169]    [Pg.170]    [Pg.320]    [Pg.249]    [Pg.338]    [Pg.88]   
See also in sourсe #XX -- [ Pg.2 , Pg.22 ]




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