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Carbonyl compds

Substrate R Sn Config. of 12 Ratio Z/E Yield <%) Carbonyl Compd Config. ee (%) Yield (%) Ref... [Pg.424]

It undergoes many condensation and addition reactions with carbonyl compds, active methylene compds, and activated olefins (Refs 10,43,... [Pg.87]

Chemical Reactions. TNMe is a strong acid and forms salts with metals and bases (see below). It readily reacts with formaldehyde to form trinitroethanol (Ref 16). it adds to activated double bonds, such as ft, J -un saturated carbonyl compds and vinyl ethers (Ref 19b). [Pg.97]

The principal organic reaction of ozone is its addition to the carbon-carbon double bond of an ethylenic compd. The resulting ozone-olefin addition compd is known as an ozonide. Decompn of the ozonide gives a mixt of oxygenated products containing carbonyl compds and acids. [Pg.469]

The primary ozone-olefin addition product splits into a molozonide zwitterion (3). The zwitterion (3) then stabilizes by splitting into a carbonyl compd (4) and another zwitterion (5). [Pg.469]

Now chemists at the Central Research Laboratories of Produits Chimiques Ugine Kuhlmann (PCUK) at Lyons, France, developed beginning in 1970, under the direction of Dr F. Weiss, a novel continuous process for manufg hydrazine. The process is based on the discovery that ammonia, hydrogen peroxide, and a carbonyl compd, such as methyl ethyl ketone, react in presence of an amide and catalytic quantities of a phosphate to form an azine intermediate. This intermediate hydrolyzes quantitatively to hydrazine and to carbonyl compd which is recycled. The yield is claimed to be better than 75%... [Pg.191]

Carbonyl Diazide (formerly called Carbonyl Nitride Carbazoimide) (Called Rohlensaure diazid, Carbazid or Sticks to ffkohlenoxyd in Ger), C0(Ns)jr mw 112.06, N 75.00% extremely volat, long ndls very sol in w, ale and eth but insol in petr eth undergoes hydrolysis to yield C03 and HN3 it has a penetraring odor and like other carbonyl compds is highly toxic and dangerous (Ref 7)... [Pg.528]

Analysis of mixts contg acetone, ethanol isopropanol) 10)H.A.Iddle C.E. Jackson,AnalChem 6,454-6(1934) (Acet, as well as other carbonyl compds, reacts quantitatively with 2,4—dinitrophenylhydrazine with formation of solid hydrazone. This procedure seems to be only approximate) 11)E.K.Nikitin, ZhPriklKhim 9,1543-6(1936)(in Fr) ... [Pg.39]

Olefin Semicon- ductor Solvent Time /h Conver sion/% - Carbonyl compds/% Epoxide or its deriv/%... [Pg.45]

USE The racemic form as reagent for the characterization of aldehydes and ketones. The optically active forms as resolving agents for carbonyl compds possessing asymmetric carbon atoms. [Pg.1158]

USE Fluorination of alcohols, carboxylic acids and carbonyl compds Olah et al. loc. cit. [Pg.1338]

Cyclohexanone oxime dissolved in ca. 2 M NaOH containing NaBH4, and refluxed 2 hrs. cyclohexanol. Y 87%. - Similarly via the Na-salt of the boric acid diester a-Hydroximinoacetophenone l-phenylethane-l,2-diol. Y 72-78%. -Oximes of conjugated carbonyl compds., such as cinnamaldehyde or acetophenone, do not react. F. e. s. K. H. Bell, Australian J. Chem. 23, 1415 (1970). [Pg.64]

Uses Dye intermediate in research and analytical chemistry fluorogenic agent for detection of carbonyl compds. [Pg.215]


See other pages where Carbonyl compds is mentioned: [Pg.422]    [Pg.307]    [Pg.736]    [Pg.39]    [Pg.308]    [Pg.737]    [Pg.39]    [Pg.199]    [Pg.205]    [Pg.215]    [Pg.219]    [Pg.284]    [Pg.473]    [Pg.1429]   


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Metal carbonyls (s. a. under compds

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