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Acid cyanides

Cyan-, of or combined with cyanogen, cyano-(as Cyanpropionadure, cyanopropionic acid), cyanide of (as Cyanammonium, ammonium cyanide), -alkali, n. alkali cyanide, -alkyl, n. alkyl cyanide. [Pg.94]

Synonym(s) Formonitrile hydrocyanic acid prussic acid Cyanide of sodium hydrocyanic acid sodium salt Cyanide of potassium hydrocyanic acid, potassium salt Calcid calcyan cyanide of calcium... [Pg.131]

ALKYL NITRATES lewis acids CYANIDES hypochlorites... [Pg.169]

ALKYL NITRATES Icwis acids CYANIDES hypochlorites DEVARDA S ALLOY DIAZONIUM TETRAHALOBORATES ISOXAZOLES NITROBENZALDEHYDES NITROBENZYL COMPOUNDS... [Pg.150]

This chapter deals with the kinetics and mechanisms of the hydrolysis of carboxylic acid derivatives of general formula RCOX. These include carboxylic acid halides, amides, and anhydrides with small sections on carboxylic acid cyanides etc. Many recent developments in this field have been made with acid derivatives in which R is not an aliphatic or aromatic group, for example, carbamic acid derivatives, and these are reported where relevant, as are reactions such as ethanolysis, aminolysis, etc. where they throw light on the mechanisms of hydrolysis. [Pg.209]

Hydrocyanic acid - [CYANIDES] (Vol 7) -atmospheric synthesis [IMINES, CYCLIC] (Vol 14)... [Pg.489]

The most recent procedure to be adopted165 employs the essentials of Scheme 12 but differs simply in the nature of the carbonyl compound employed aldehydes and ketones are replaced by acid chlorides or acid cyanides. At the time of writing this procedure has been applied to the naphthalene series only to give 96 containing alkyl, electron-donating and electron-withdrawing groups at the exocyclic position (Scheme 13). The specific... [Pg.731]

Odour of hydrocyanic acid—cyanide, ferro- or ferri-cyanide. [Pg.517]

Selectivity in the reaction of cysteamine with diphenylphos-phinic acid cyanide ... [Pg.15]

The US Army Medical Research Institute of Chemical Defence employs an automated microdistillation assay for cyanide in blood, using fluorometric detection (67). For assaying free CN , plasma is mixed with and dialyzed against pH 7.4 phosphate buffer. For an assay of total blood cyanide, blood is mixed with saline containing Triton X (which hemolyzes the red cells), treated with 0.5 % sulfuric acid and dialyzed against 0.25 % sulfuric acid. Cyanide is... [Pg.424]

Cyanide will attack iminium ions the Strecker synthesis of amino acids Cyanide will react with iminium ions to form oc amino nitriles. Although these compounds are relatively unimportant in their own right, a simple hydrolysis step produces a amino acids. This route to amino acids is known as the Strecker synthesis. Of course, it s not usually necessary to make the amino acids that Nature produces for us in living systems they can be extracted from hydrolysed proteins. [Pg.356]

Solutions of the a salt, upon prolonged standing, are converted into the j8 variety, a process that is hastened by the addition of 1 per cent, of acetic acid. Cyanides, alkalies, and ammonia induce the reverse transformation. [Pg.214]

Common Name(s) Blue Acid, Cyanide, Cyclone B, KCN, HCN, Prussic Acid, Zyklon-B Dosage .56oz (i6g)... [Pg.29]

Aqueous solution is acidic. Contact with acid or acid fumes forms toxic fluorine. Keep away from strong oxidizers strong acids cyanides, alkalis, alkaline metals and finely divided aluminum or magnesium. In tenqjeratures above 100°F/38°C, toxic fumes of ammonia, hydrogen fluoride, nitrogen oxides, silicon oxide, and silicon tetrafluoride maybe released. On small fires, use dry chemical powder (such as Purple-K-... [Pg.70]


See other pages where Acid cyanides is mentioned: [Pg.385]    [Pg.44]    [Pg.74]    [Pg.74]    [Pg.95]    [Pg.191]    [Pg.132]    [Pg.151]    [Pg.50]    [Pg.153]    [Pg.132]    [Pg.304]    [Pg.385]    [Pg.823]    [Pg.424]    [Pg.425]    [Pg.222]    [Pg.26]    [Pg.27]    [Pg.280]    [Pg.533]    [Pg.3]    [Pg.1072]    [Pg.2564]    [Pg.646]    [Pg.1793]    [Pg.193]    [Pg.3]    [Pg.216]    [Pg.532]    [Pg.115]    [Pg.539]    [Pg.165]   


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Acetic acid, phenylacyl cyanide synthesis

Acetic acid, phenylacyl cyanide synthesis Schmidt reaction

Acetic acid, phenylacyl cyanide synthesis acyloin coupling reaction

Acid cyanides Claisen condensation

Acid cyanides decarbonylation

Acid cyanides palladium-catalyzed

Acidity continued hydrogen cyanide

Addition of hydrogen cyanide to an aldehyde. Mandelic acid from benzaldehyde

Aromatic acids from cyanides

Benzyl cyanide hydrolysis to acid

Cinnamic acid acyl cyanides

Condensation, of acetoacetic ester, acid with sodium cyanide and hydrazine

Cyanide-plating baths acid electrolytes

Cyanides alkynes: acidic hydrogen

Cyanides, weak-acid dissociable

Hydrocyanic Acid—Hydrogen Cyanide

Hydrocyanic acid and the cyanide ion

Hydrocyanic acid cyanide

Hydrogen cyanide acidity

Hydrogen cyanide, acid dissociation constant

Hydrolysis, amide to acid of benzyl cyanide

Lewis acids sodium cyanide

Lewis acids with potassium cyanide

Oxidation, by nitric acid of cyanide ion with iodine

Phenylacetic acid (from benzyl cyanide)

Ribofuranosyl cyanide via Lewis acid promoted reaction

Silyl cyanides, trialkylreactions with carbonyl compounds Lewis acid promotion

Trimethylsilyl cyanide , Strecker amino acid synthesis

Valeric acid (hydrolysis of n-butyl cyanide)

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