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Carbonyl compounds Norrish type I reaction

In general, the n,Jt excited ketones undergo much faster cleavage than those with a lowest 7t,7t excited state, because the O-orbital of a bond being cleaved overlaps with the half-vacant n-orbital on the oxygen atom.905,911,919 The cleavage rate constant of the n,jt triplet excited benzyl phenyl ketone (PhCH2COPh) is, for example, more than three orders [Pg.305]

Case Study 6.19 Photochemistry in crystals - solid-to-solid photoreaction [Pg.309]


See other pages where Carbonyl compounds Norrish type I reaction is mentioned: [Pg.203]    [Pg.289]    [Pg.305]    [Pg.380]   


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Carbonyl compounds Norrish type

Carbonyl compounds, reactions

Compound types

Compounding types

I compounds

I----, reactions

Norrish

Norrish I reaction

Norrish Type 1 reactions

Norrish Type I Cleavage Reaction of Carbonyl Compounds

Norrish reaction

Norrish type

Norrish type I reaction

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