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hydrocyanic

hydrocyanic Sentence Examples

  • Ustilago, and filling a greenhouse with hydrocyanic acid gas when young insects are commencing their ravages, e.g.

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  • Carbolic acid is distinguished from all other acids so-called - except oxalic acid and hydrocyanic acid - in that it is a neurotic poison, having a marked action directly upon the nervous system.

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  • This compound combines with hydrocyanic acid to form a nitrile which hydrolyses to dichlorhydroxy iso-butyric acid.

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  • The acetone dicarboxylic acid, CO(CH 2 CO 2 H) 2, so obtained combines with hydrocyanic acid, and this product yields citric acid on hydrolysis.

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  • Instances had already been recorded of cases where a halogen element replaced hydrogen with the production of a closely allied substance: Gay Lussac had prepared cyanogen chloride from hydrocyanic acid; Faraday, hexachlorethane from ethylene dichloride, &c. Here the electronegative halogens exercised a function similar to electro-positive hydrogen.

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  • Cyanogen and hydrocyanic acid, recognizable by their odour, indicate decomposable cyanides.

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  • From this he infers that cyanogen is C: N N :C and not N; C C; N, that hydrocyanic acid is HC N, and acetonitrile CH 3 C; N.

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  • Glucoseoxime on warming with acetic anhydride is simultaneously acetylated and dehydrated, yielding an acetylated gluconitrile, which when warmed with ammoniacal silver nitrate loses hydrocyanic acid and is transformed into an acetyl pentose.

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  • The aldehyde group reacts with hydrocyanic acid to produce two stereo-isomeric cyanhydrins; this isomerism is due to the conversion of an originally non-asymmetric carbon atom into an asymmetric one.

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  • With hydrocyanic acid aldehydes form the cyanhydrins R�CH(OH)�CN.

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  • The remaining oxygen atom is aldehydic or ketonic, for the sugars combine with hydrocyanic acid, hydroxylamine and phenylhydrazine.

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  • Wohl forms the oxime and converts it into an acetylated nitrile by means of acetic anhydride and sodium acetate; ammoniacal silver nitrate solution removes hydrocyanic acid and the resulting acetate is hydrolysed by acting with ammonia to form an amide, which is finally decomposed with sulphuric acid.

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  • When xylose is combined with hydrocyanic acid and the cyanide is hydrolysed, together with l-gulonic acid, a second isomeric acid, l-idonic acid, is produced, which on reduction yields the hexaldose l-idose.

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  • CYANIDE, in chemistry, a salt of prussic or hydrocyanic acid, the name being more usually restricted to inorganic salts, i.e.

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  • The existence of acids not containing oxygen was, in itself, sufficient to overthrow this idea, but, although Berthollet had shown, in 1789, that sulphuretted hydrogen (or hydrosulphuric acid) contained no oxygen, Lavoisier's theory held its own until the researches of Davy, Gay-Lussac and Thenard on hydrochloric acid and chlorine, and of Gay-Lussac on hydrocyanic acid, established beyond all cavil that oxygen was not essential to acidic properties.

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  • It is also obtained by the action of hydrogen peroxide on hydrocyanic acid, or of manganese dioxide and sulphuric acid on potassium cyanide.

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  • In The Latter Reaction Various Other Compounds, Such As Carbon Dioxide, Carbon Bisulphide And Hydrocyanic Acid, Are Produced.

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  • PRUSSIC ACID, or Hydrocyanic Acid, Hcn, an organic acid first prepared in1782-1783by C. Scheele and subsequently examined by J.

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  • The salts of this acid, known as cyanides, may be prepared by the action of cyanogen or of gaseous hydrocyanic acid on a metal; by heating the carbonates or hydrooxides of the alkali metals in a current of hydrocyanic acid; by heating alkaline carbonates with carbon in the presence of free nitrogen: BaCO 3 + 4 C + N2 = Ba(NC) 2 + 3C0; by ignition of nitrogenous organic substances in the presence of alkaline carbonates or hydroxides; or by processes of double decomposition.

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  • Mercuric cyanide, Hg(NC)2, is a sparingly soluble salt formed by dissolving precipitated mercuric oxide in hydrocyanic acid, or by boiling potassium ferrocyanide with mercuric sulphate and water: 2K4Fe(NC)6+3HgS04=3Hg(NC)2+ 3K 2 SO 4 -{-K 2 Fe[Fe(NC) 6 ].

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  • Dilute mineral acids decompose it with the formation of insoluble silver cyanide and hydrocyanic acid: KNC AgNC+HN03=HCN+ KNO 3 +AgNC. A boiling solution of potassium chloride with the double cyanide gives silver chloride and potassium cyanide.

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  • Potassium cyanide, KNC, and sodium cyanide, NaNC, are two of the most important of the salts of hydrocyanic acid, the former being manufactured in large quantities for consumption in the extraction of gold.

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  • The double cyanides formed by the solution of the cyanide of a heavy metal in a solution of potassium cyanide are decomposed by mineral acids with liberation of hydrocyanic acid and formation of the cyanide of the heavy metal.

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  • 9474 (1892)] passes the gas (after freeing it from ammonia) through a solution of potassium carbonate containing ferric oxide or ferrous carbonate (actually ferrous sulphate and potassium carbonate) in suspension; the sulphuretted hydrogen in the gas probably converts the iron salts into ferrous sulphide which then, in the presence of the hydrocyanic acid in the gas, and the alkaline carbonate, forms the ferrocyanide, thus: FeS+6HCN+ 2K 2 CO 3 = K 4 Fe(NC) 6 + H 2 S + 2CO 2 + 2H 2 0.

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  • When fused with potassium carbonate it yields potassium cyanide; warmed with dilute sulphuric acid it yields hydrocyanic acid, but with concentrated sulphuric acid it yields carbon monoxide: 6H 2 O + K 4 Fe(NC) 6 + 6H 2 SO 4 = 2K 2 SO 4 + FeSO 4 + 3(NH4)2S04 + 6C0.

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  • - Hydrocyanic acid forms two series of derivatives by the exchange of its hydrogen atom for alkyl or aryl groups; namely the nitriles, of type R CN, and the isonitriles, of type R NC. The latter compounds may be considered as derivatives of the as yet unknown isohydrocyanic acid HNC.

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  • As an alternative test the cyanide may be decomposed by dilute hydrochloric acid, and the liberated hydrocyanic acid absorbed in a little yellow ammonium sulphide.

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  • The amount of hydrocyanic acid in a solution may be determined by adding excess of caustic potash and a small quantity of an alkaline chloride, and running into the dilute solution standard silver nitrate until a faint permanent turbidity (of silver chloride) is produced, that is, until the reaction, 2KNC+AgNO 3 = KAg(NC) 2 - -KNO 3, is completed.

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  • Hydrocyanic acid is a protoplasmic poison, directly lethal to all living tissues, whether in a plant or an animal.

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  • Hydrolysis of hydrocyanic acid by means of hydrochloric acid yields formic acid.

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  • It possesses all the characteristic properties of an aldehyde; being readily oxidized to benzoic acid; reducing solutions of silver salts; forming addition products with hydrogen, hydrocyanic acid and sodium bisulphite; and giving an oxime and a hydrazone.

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  • Heated with sulphur it forms benzoic acid and stilbene: 2C 7 H 6 0+S = C6HS000H+C6H5CHS, 2C 6 H 5 CHS =2S +C14H12 Its addition compound with hydrocyanic acid gives mandelic acid C 6 H 5 CH(OH) COOH on hydrolysis; when heated with sodium succinate and acetic anhydride, phenyl-iso-crotonic acid C 6 H 5 CH: CH CH 2 000H is produced, which on boiling is converted into a-naphthol C 10 H 7 0H.

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  • Certain solvents, such as water, liquid ammonia or liquid hydrocyanic acid, possess the power of making some solutes, such as mineral salts and acids, when dissolved in them, conductors of electricity.

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  • They combine with hydrocyanic acid to form nitriles, which on hydrolysis furnish hydroxyacids, (CH3)2C0 -> (CH 3) 2 C OH CN - (CH3)2 C OH C02H; with phenylhydrazine they yield hydrazones; with hydrazine they yield in addition ketazines RR' C:N N:C RR' (T.

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  • It combines with sodium bisulphite and with hydrocyanic acid.

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  • Similar results have been obtained by using diazotized para-anisidine, a synand an anticompound being formed, as well as a third isomeric cyanide, obtained by evaporating para-methoxybenzenediazonium hydroxide in the presence of an excess of hydrocyanic acid at ordinary temperatures.

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  • By the action of bleaching powder on methylamine hydrochloride, there is obtained a volatile liquid (methyldichloramine, CH 3 -N C1 2), boiling at 58-60° C., which explodes violently when heated with water, yielding hydrocyanic acid (CH 3 NC1 2 =HCN+2HC1).

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  • It may be condensed to a liquid, which boils at about o° C. It is a powerful methylating agent, reacting with water to form methyl alcohol, and converting acetic acid into methylacetate, hydrochloric acid into methyl chloride, hydrocyanic acid into acetonitrile, and phenol into anisol, nitrogen being eliminated in each case.

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  • It crystallizes in prisms which melt at 121° C. It yields addition compounds with aniline and naphthalene, and combines directly with potassium methylate, sodio-malonic ester and hydrocyanic ester.

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  • It undoubtedly contains a keto-group, for it reacts with hydrocyanic acid, hydroxylamine, phenylhydrazine and ammonia; sodium bisulphite also combines with it to form a crystalline compound, hence it contains the grouping CH 3 �CO-.

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  • Irritation is lessened by lotions containing substances that will diminish irritability of the nerve-endings and skin, such as carbolic acid, hydrocyanic acid, morphine or opium, cocaine, belladonna or atropine.

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  • It combines with water, forming the hydrates SbC1 5 -1-1 2 0 and SbC1 3.4H 2 O; it also combines with phosphorus oxychloride, hydrocyanic acid, and cyanogen chloride.

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  • It also unites directly with hydrocyanic acid to form the nitrile of a-oxyisobutyric acid.

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  • Kdnigs, Ber., 1879, 12, p. 2341) by passing a mixture of acetylene and hydrocyanic acid through a red-hot tube (W.

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  • It reacts with the caustic alkalis to form selenites, and combines directly with hydrocyanic acid.

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  • Atkinson Butterfield gives the composition of the gas at this It happens that ammonia, being a strong base, will effect the extraction of a certain proportion of such compounds as sulphuretted hydrogen, carbon dioxide and hydrocyanic acid, and the gas is now washed with water and ammoniacal liquor.

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  • - This includes compounds of cyanogen such as hydrocyanic (prussic) acid, cyanides of potassium, sodium, &c., cherry-laurel water, amygdalin, bitter almonds and other chemical and vegetable substances which readily yield hydrocyanic acid.

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  • Hydrocyanic acid is a general protoplasmic poison, all the lower organisms being very susceptible to its action, while in the higher animals it speedily depresses or paralyses all forms of nerve tissue.

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  • Cobaltous cyanide, Co(CN)2.3H20, is obtained when the carbonate is dissolved in hydrocyanic acid or when the acetate is precipitated by potassium cyanide.

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  • It dissolves readily in water and the aqueous solution decomposes on standing; a dark-brown flocculent precipitate of azulmic acid, C 4 H 5 N 5 0, separating whilst ammonium oxalate, urea and hydrocyanic acid are found in the solution.

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  • In many respects it resembles chlorine in its chemical behaviour, a circumstance noted by Gay-Lussac; it combines directly with hydrogen (at 50o° to 550° C.) to form hydrocyanic acid, and with chlorine, bromine, iodine and sulphur, to form cyanogen chloride, &c.; it also combines directly with zinc, cadmium and iron to form cyanides of these metals.

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  • It shows characteristic ketone reactions, yielding a bisulphite compound and combining with hydrocyanic acid to form the nitrile of a-oxyisosuccinic acid.

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  • Ustilago, and filling a greenhouse with hydrocyanic acid gas when young insects are commencing their ravages, e.g.

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  • Carbolic acid is distinguished from all other acids so-called - except oxalic acid and hydrocyanic acid - in that it is a neurotic poison, having a marked action directly upon the nervous system.

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  • This compound combines with hydrocyanic acid to form a nitrile which hydrolyses to dichlorhydroxy iso-butyric acid.

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  • The acetone dicarboxylic acid, CO(CH 2 CO 2 H) 2, so obtained combines with hydrocyanic acid, and this product yields citric acid on hydrolysis.

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  • Instances had already been recorded of cases where a halogen element replaced hydrogen with the production of a closely allied substance: Gay Lussac had prepared cyanogen chloride from hydrocyanic acid; Faraday, hexachlorethane from ethylene dichloride, &c. Here the electronegative halogens exercised a function similar to electro-positive hydrogen.

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  • Cyanogen and hydrocyanic acid, recognizable by their odour, indicate decomposable cyanides.

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  • From this he infers that cyanogen is C: N N :C and not N; C C; N, that hydrocyanic acid is HC N, and acetonitrile CH 3 C; N.

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  • Glucoseoxime on warming with acetic anhydride is simultaneously acetylated and dehydrated, yielding an acetylated gluconitrile, which when warmed with ammoniacal silver nitrate loses hydrocyanic acid and is transformed into an acetyl pentose.

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  • The aldehyde group reacts with hydrocyanic acid to produce two stereo-isomeric cyanhydrins; this isomerism is due to the conversion of an originally non-asymmetric carbon atom into an asymmetric one.

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  • It may be prepared by the action of hydrochloric acid on the addition compound of benzaldehyde and hydrocyanic acid: C 6 H 5 CHO-HCN+HC1+2H 2 O= C6H5 [[Choh 000h+Nh4c1, (F.

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  • With hydrocyanic acid aldehydes form the cyanhydrins R�CH(OH)�CN.

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  • The remaining oxygen atom is aldehydic or ketonic, for the sugars combine with hydrocyanic acid, hydroxylamine and phenylhydrazine.

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  • Wohl forms the oxime and converts it into an acetylated nitrile by means of acetic anhydride and sodium acetate; ammoniacal silver nitrate solution removes hydrocyanic acid and the resulting acetate is hydrolysed by acting with ammonia to form an amide, which is finally decomposed with sulphuric acid.

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  • When xylose is combined with hydrocyanic acid and the cyanide is hydrolysed, together with l-gulonic acid, a second isomeric acid, l-idonic acid, is produced, which on reduction yields the hexaldose l-idose.

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  • CYANIDE, in chemistry, a salt of prussic or hydrocyanic acid, the name being more usually restricted to inorganic salts, i.e.

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  • The existence of acids not containing oxygen was, in itself, sufficient to overthrow this idea, but, although Berthollet had shown, in 1789, that sulphuretted hydrogen (or hydrosulphuric acid) contained no oxygen, Lavoisier's theory held its own until the researches of Davy, Gay-Lussac and Thenard on hydrochloric acid and chlorine, and of Gay-Lussac on hydrocyanic acid, established beyond all cavil that oxygen was not essential to acidic properties.

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  • It is also obtained by the action of hydrogen peroxide on hydrocyanic acid, or of manganese dioxide and sulphuric acid on potassium cyanide.

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  • In The Latter Reaction Various Other Compounds, Such As Carbon Dioxide, Carbon Bisulphide And Hydrocyanic Acid, Are Produced.

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  • PRUSSIC ACID, or Hydrocyanic Acid, Hcn, an organic acid first prepared in1782-1783by C. Scheele and subsequently examined by J.

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  • The salts of this acid, known as cyanides, may be prepared by the action of cyanogen or of gaseous hydrocyanic acid on a metal; by heating the carbonates or hydrooxides of the alkali metals in a current of hydrocyanic acid; by heating alkaline carbonates with carbon in the presence of free nitrogen: BaCO 3 + 4 C + N2 = Ba(NC) 2 + 3C0; by ignition of nitrogenous organic substances in the presence of alkaline carbonates or hydroxides; or by processes of double decomposition.

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  • Mercuric cyanide, Hg(NC)2, is a sparingly soluble salt formed by dissolving precipitated mercuric oxide in hydrocyanic acid, or by boiling potassium ferrocyanide with mercuric sulphate and water: 2K4Fe(NC)6+3HgS04=3Hg(NC)2+ 3K 2 SO 4 -{-K 2 Fe[Fe(NC) 6 ].

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  • Dilute mineral acids decompose it with the formation of insoluble silver cyanide and hydrocyanic acid: KNC AgNC+HN03=HCN+ KNO 3 +AgNC. A boiling solution of potassium chloride with the double cyanide gives silver chloride and potassium cyanide.

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  • Potassium cyanide, KNC, and sodium cyanide, NaNC, are two of the most important of the salts of hydrocyanic acid, the former being manufactured in large quantities for consumption in the extraction of gold.

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  • The double cyanides formed by the solution of the cyanide of a heavy metal in a solution of potassium cyanide are decomposed by mineral acids with liberation of hydrocyanic acid and formation of the cyanide of the heavy metal.

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  • 9474 (1892)] passes the gas (after freeing it from ammonia) through a solution of potassium carbonate containing ferric oxide or ferrous carbonate (actually ferrous sulphate and potassium carbonate) in suspension; the sulphuretted hydrogen in the gas probably converts the iron salts into ferrous sulphide which then, in the presence of the hydrocyanic acid in the gas, and the alkaline carbonate, forms the ferrocyanide, thus: FeS+6HCN+ 2K 2 CO 3 = K 4 Fe(NC) 6 + H 2 S + 2CO 2 + 2H 2 0.

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  • When fused with potassium carbonate it yields potassium cyanide; warmed with dilute sulphuric acid it yields hydrocyanic acid, but with concentrated sulphuric acid it yields carbon monoxide: 6H 2 O + K 4 Fe(NC) 6 + 6H 2 SO 4 = 2K 2 SO 4 + FeSO 4 + 3(NH4)2S04 + 6C0.

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  • - Hydrocyanic acid forms two series of derivatives by the exchange of its hydrogen atom for alkyl or aryl groups; namely the nitriles, of type R CN, and the isonitriles, of type R NC. The latter compounds may be considered as derivatives of the as yet unknown isohydrocyanic acid HNC.

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  • As an alternative test the cyanide may be decomposed by dilute hydrochloric acid, and the liberated hydrocyanic acid absorbed in a little yellow ammonium sulphide.

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  • The amount of hydrocyanic acid in a solution may be determined by adding excess of caustic potash and a small quantity of an alkaline chloride, and running into the dilute solution standard silver nitrate until a faint permanent turbidity (of silver chloride) is produced, that is, until the reaction, 2KNC+AgNO 3 = KAg(NC) 2 - -KNO 3, is completed.

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  • Hydrocyanic acid is a protoplasmic poison, directly lethal to all living tissues, whether in a plant or an animal.

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  • Hydrolysis of hydrocyanic acid by means of hydrochloric acid yields formic acid.

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  • It may also be prepared by oxidizing benzyl alcohol with concentrated nitric acid; by distilling a mixture of calcium benzoate and calcium formate; by the condensation of chlor-oxalic ester with benzene in the presence of aluminium chloride, the ester of the ketonic acid formed being then hydrolysed and the resulting acid distilled: C 6 H 6 +Cl CO Cooc 2 H 5 = C,H5co COOC2H5d-HC1, C 6 H 5 CO 000H =C6H5CHO+C02; by the action of anhydrous hydrocyanic acid and hydrochloric acid on benzene, an aldime being formed as an intermediate product: C 6 H 6 +HCN+HC1= C6H5CH :NH HC1, Benzaldine hydrochloride C 6 H 5 CH: NH HC1+H 2 O =NH4C1+C6H5CHO; and by the action of chromium oxychloride on toluene dissolved in carbon bisulphide (A.

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  • It possesses all the characteristic properties of an aldehyde; being readily oxidized to benzoic acid; reducing solutions of silver salts; forming addition products with hydrogen, hydrocyanic acid and sodium bisulphite; and giving an oxime and a hydrazone.

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  • Heated with sulphur it forms benzoic acid and stilbene: 2C 7 H 6 0+S = C6HS000H+C6H5CHS, 2C 6 H 5 CHS =2S +C14H12 Its addition compound with hydrocyanic acid gives mandelic acid C 6 H 5 CH(OH) COOH on hydrolysis; when heated with sodium succinate and acetic anhydride, phenyl-iso-crotonic acid C 6 H 5 CH: CH CH 2 000H is produced, which on boiling is converted into a-naphthol C 10 H 7 0H.

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  • Certain solvents, such as water, liquid ammonia or liquid hydrocyanic acid, possess the power of making some solutes, such as mineral salts and acids, when dissolved in them, conductors of electricity.

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  • The remedy is to spray with kerosene emulsion or whale-oil soap; or if on cucumbers or tomatoes, it is best to fumigate with hydrocyanic acid gas, using one ounce of potassium cyanide to each woo cubic ft.

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  • They combine with hydrocyanic acid to form nitriles, which on hydrolysis furnish hydroxyacids, (CH3)2C0 -> (CH 3) 2 C OH CN - (CH3)2 C OH C02H; with phenylhydrazine they yield hydrazones; with hydrazine they yield in addition ketazines RR' C:N N:C RR' (T.

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  • It combines with sodium bisulphite and with hydrocyanic acid.

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  • Similar results have been obtained by using diazotized para-anisidine, a synand an anticompound being formed, as well as a third isomeric cyanide, obtained by evaporating para-methoxybenzenediazonium hydroxide in the presence of an excess of hydrocyanic acid at ordinary temperatures.

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  • By the action of bleaching powder on methylamine hydrochloride, there is obtained a volatile liquid (methyldichloramine, CH 3 -N C1 2), boiling at 58-60° C., which explodes violently when heated with water, yielding hydrocyanic acid (CH 3 NC1 2 =HCN+2HC1).

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  • It may be condensed to a liquid, which boils at about o° C. It is a powerful methylating agent, reacting with water to form methyl alcohol, and converting acetic acid into methylacetate, hydrochloric acid into methyl chloride, hydrocyanic acid into acetonitrile, and phenol into anisol, nitrogen being eliminated in each case.

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  • It crystallizes in prisms which melt at 121° C. It yields addition compounds with aniline and naphthalene, and combines directly with potassium methylate, sodio-malonic ester and hydrocyanic ester.

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  • It undoubtedly contains a keto-group, for it reacts with hydrocyanic acid, hydroxylamine, phenylhydrazine and ammonia; sodium bisulphite also combines with it to form a crystalline compound, hence it contains the grouping CH 3 �CO-.

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  • Irritation is lessened by lotions containing substances that will diminish irritability of the nerve-endings and skin, such as carbolic acid, hydrocyanic acid, morphine or opium, cocaine, belladonna or atropine.

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  • It combines with water, forming the hydrates SbC1 5 -1-1 2 0 and SbC1 3.4H 2 O; it also combines with phosphorus oxychloride, hydrocyanic acid, and cyanogen chloride.

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  • It also unites directly with hydrocyanic acid to form the nitrile of a-oxyisobutyric acid.

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  • Kdnigs, Ber., 1879, 12, p. 2341) by passing a mixture of acetylene and hydrocyanic acid through a red-hot tube (W.

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  • It reacts with the caustic alkalis to form selenites, and combines directly with hydrocyanic acid.

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  • The corresponding oxyacid is obtained by the hydrolysis of the nitrile, which is formed by the addition of hydrocyanic acid to suberone (A.

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  • Atkinson Butterfield gives the composition of the gas at this It happens that ammonia, being a strong base, will effect the extraction of a certain proportion of such compounds as sulphuretted hydrogen, carbon dioxide and hydrocyanic acid, and the gas is now washed with water and ammoniacal liquor.

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  • - This includes compounds of cyanogen such as hydrocyanic (prussic) acid, cyanides of potassium, sodium, &c., cherry-laurel water, amygdalin, bitter almonds and other chemical and vegetable substances which readily yield hydrocyanic acid.

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  • Hydrocyanic acid is a general protoplasmic poison, all the lower organisms being very susceptible to its action, while in the higher animals it speedily depresses or paralyses all forms of nerve tissue.

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