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It antibonding molecular orbital

Compared to an H atom, electrons with the function y/, are less energetic, and those with the function y/2 are more energetic. When the two available electrons occupy the molecular orbital y/(, this is energetically favorable y/, is the wave function of a bonding molecular orbital. y/2 belongs to an antibonding molecular orbital its occupation by electrons requires the input of energy. [Pg.86]

The third step hypothesized [eq. (9)] is electron demotion from the singly occupied antibonding molecular orbital of XIII to the low energy, singly occupied oxygen p orbital which originally lost the electron in the n-ir excitation process. It is important and of interest to note that this demotion process is an electronic transition thus XIII and XIV are... [Pg.189]

For a 7t system to function as an electron acceptor, it must have unfilled orbitals available to accept electrons. In the case of olefins or dienes those are n antibonding molecular orbitals. Thus interaction of the HOMO of one n system with file LUMO of a second n system produces a donor-acceptor pair (HOMO donating to LUMO) enabling electrons to be transferred from one n system to another with resulting bond formation. [Pg.313]


See other pages where It antibonding molecular orbital is mentioned: [Pg.395]    [Pg.967]    [Pg.967]    [Pg.26]    [Pg.357]    [Pg.77]    [Pg.395]    [Pg.967]    [Pg.967]    [Pg.26]    [Pg.357]    [Pg.77]    [Pg.169]    [Pg.735]    [Pg.244]    [Pg.809]    [Pg.147]    [Pg.299]    [Pg.24]    [Pg.169]    [Pg.136]    [Pg.79]    [Pg.479]    [Pg.243]    [Pg.255]    [Pg.11]    [Pg.13]    [Pg.328]    [Pg.47]    [Pg.68]    [Pg.24]    [Pg.95]    [Pg.130]    [Pg.125]    [Pg.46]    [Pg.72]    [Pg.136]    [Pg.995]    [Pg.98]    [Pg.99]    [Pg.715]    [Pg.213]    [Pg.239]    [Pg.275]    [Pg.185]    [Pg.279]    [Pg.236]    [Pg.17]    [Pg.144]    [Pg.141]    [Pg.61]    [Pg.7]   
See also in sourсe #XX -- [ Pg.41 ]




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