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Oxidative cleavage, degradation from carbonyl compounds

More powerful oxidants are almost always needed. Those commonly used for cleavage of olefins — and for other degradations — include nitric acid, hydrogen peroxide, permanganate, chromic acid, very concentrated alkali hydroxides, and in particular ozone. The products to be expected from oxidative fission of an ethylenic carbon-carbon double bond are carbonyl compounds — an aldehyde or a ketone or both according as the doubly bonded carbon atoms do or do not carry a hydrogen atom — but it often happens that 1,2-glycols are obtained as intermediates. [Pg.1036]


See other pages where Oxidative cleavage, degradation from carbonyl compounds is mentioned: [Pg.201]    [Pg.256]    [Pg.341]    [Pg.697]    [Pg.506]    [Pg.394]    [Pg.324]    [Pg.93]    [Pg.284]   
See also in sourсe #XX -- [ Pg.45 ]




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Carbonyl compounds cleavage

Carbonyl oxidation

Carbonyl oxide

Carbonylation oxide

Carbonyls 3-cleavage

From carbonyl compounds

OXIDATION OXIDATIVE DEGRADATION

Oxidation carbonylative

Oxidation oxidative carbonylation

Oxidations degradative oxidation

Oxidative carbonylation

Oxidative carbonylations

Oxidative degradation

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