Cyanide is a group that contains C≡N triple bond and it is a chemical compound. C≡N is also called a Cyano group. The anion CN‾ exists in the cyanide group belong to the inorganic cyanide. Formula: CN‾ conjugate acid: Hydrogen cyanide
The compounds are more harmful is potassium cyanide and sodium Cyanide, which is known as Cyanide salts. HCN or hydrocyanic acid and is a more volatile liquid and volatile organic compunds which is formed in industries on a massive scale and it is also known as hydrogen cyanide. By the Acidification of cyanide salts, we get the cyanide.
Nitriles are known for organic cyanide. CN group is covalently bonded to the carbon atom in nitriles. e.g there is a covalent bond between methyl (CH₃) and cyanide group in acetonitrile. Whereas cyanide is not released by them, nitriles are commonly low toxic than cyanide salts. Few nitriles that exist naturally as cyanohydrin liberate hydrogen cyanide.
Nomenclature and the etymology of cyanide | Acetonitrile and methyl cyanide
Organic compounds whose functional group is –C≡N are known as nitriles in IUPAC nomenclature of cyanide. Therefore nitriles are known as organic compounds. e.g methyl cyanide is known for the nitrile CH₃CN which is known as acetonitrile. Cyanide ions are not discharged by the nitriles.
if the cyanide and hydroxyl are bonded to a similar carbon atom having a functional group are called cyanohydrins. In contrast to the nitriles, hydrogen cyanide is also discharged by the cyanohydrin. If C≡N‾ ion is present in salts it is known as cyanides in organic chemistry.
It is the Greek word kyanos which means dark blue as it is first received by the warmth of the pigment which is called as Prussian blue. Bonding. With the molecular nitrogen and with carbon monoxide cyanide ion exists as isoelectronic.
The occurrence of cyanide in nature | environmental cyanide
Some bacteria, fungi, and algae formed cyanides and present in many plants. Cyanides are present in abundant quantities in fruit stones and many seeds such as peaches, apples, apricot, and acrid almond.
Cyanides are present in plants in the mode of cyanogenic glycosides which are commonly constrained to the molecules of sugar and protect the plant from an herbivore.
Roots of cassava that are also known as manioc a necessary food like a potato that is overgrown in the countries of tropics also consist of cyanogenic glycosides.
The Bamboo plant cathariostachys madagascariensis that are produced in the Madagascar island also formed cyanide that is used as preventive to the grazing. The golden bamboo lemur that takes food from bamboo in comeback has established more sensitivity to cyanide.
The identification of cyanide radicle takes place in interstellar space. The temperature of clouds of interstellar gas is measured by the cyanide radicle that is also known as cyanogen.
Pyrolysis and combustion product.
In the pyrolysis and combustion of some materials underneath the conditions of deficient oxygen formed the hydrogen cyanide. e.g it is distinguished by the smoke of tobacco and burn out of internal combustion engines. When the burning or heating of some plastics that are taken from acrylonitrile liberate the hydrogen cyanide.
Organic derivatives of cyanide
The nucleophilicity of cyanide anions is higher in organic molecules cyano group is promptly originated by the halide group displacement for example in methyl chloride the chloride ion is present. In common nitriles are known for organic cyanide. CH₃CN is known as methyl cyanide but in general, it is called acetonitrile.
By keeping the functional capability cyanide which is a C-1 synthon in organic synthesis is used to elongate the carbon chain by one.
Manufacturing of cyanides
Russow process is the only prominent case that prepares cyanides. In this, process by the existence of platinum catalyst and oxygen the gaseous hydrogen cyanide is formed from ammonia and methane.
Cyanide of sodium is formed by the dissolution of gaseous hydrogen cyanide in the sodium hydroxide solution which is present in aqueous form.
Toxic effects of cyanides
Some cyanides are more harmful. In the electron transport chain at the fourth complex, the cytochrome c oxidase enzyme inhibits the anion of cyanide that is present in the eukaryotic cell in the mitochondrial membrane. In this protein, it bends to the iron.
As a consequence, the cell does not form ATP for energy in aerobic form and the disruption of the electron transport chain takes place. In hemotoxic hypoxia, the tissues that are more dependent on aerobic respiration which is specifically afflicted are the heart and central nervous system.
Hydrogen cyanide which is a more haphazard compound is a gas and killed the man by inhaled this gas. As a result, when we worked with hydrogen cyanide an air respirator is used as a source of external oxygen.
Hydrogen cyanide is formed by the addition of an acid in a cyanide salt solution. Hydrogen cyanide gas is not ejected from cyanide if it is present in alkaline solution and it is safe to use.
Only a small quantity of approximately 200 mg is injected through the mouth can cause death in minutes. Cyanide ions are not easily released by organic nitrile and it is less toxic. On the other hand trimethylsilyl cyanide easily eject cyanide ions on the contraction with water.
Treatment of cyanide exposure | Antidote of cyanide
On reaction with cyanide, hydroxocobalamin produces cyanocobalmin which is ejected from the kidneys. This process has an advantage by staying out of the constitution of methemoglobin. U.S.FDA has formalized the cyanide antidote kit which is solid underneath the grade name cyan kit. Amyl nitrile pearls, sodium thiosulphate, and sodium nitrile are included in the older cyanide antidote kit.
The aim of the antidote is to form a ferric iron pool that contends with cytochrome a₃ for cyanide. on the oxidation of hemoglobin to methemoglobin nitrites oxidase that contends for the cyanide ion with cytochrome oxidase. The main mechanism to protect the body from cyanide is the conversion to thiocyanate by enzyme and this process takes place with the help of mitochondrial enzyme rhodanese.
Kidneys excrete the thiocyanate and it is non – toxic molecule. If we accelerate the detoxification sulfur donor from the sodium thiosulphate for rhodanese so that to produce thiocyanate.
Sensitivity of cyanide
If the risk is at a minimum level then we cannot protect it because the less toxic effects are shown such as asthma, bronchitis, and hypersensitivity.
Application and uses of cyanide
Illegal fishing and poaching by cyanide
In the market of seafood and coral reefs, fishes are obtained illegitimately by the cyanide. this method is disputatious and hazardous but benefits able for the exotic fish market. In Africa cyanide is used to a toxic small pond where animals drink water by poachers to annihilate the elephant to get the ivory.
Mining through cyanide
By the mining of silver and gold cyanide is formed. In this process, their metals and ores are dissolved. In this process mixing of cyanide and minute high-grade ores and it is added 2 kg NACN as per ton concentration.
The assemblage of low-grade ores into a large quantity and it is sprayed onto a solution of cyanide about 1 kg of NACN is added in 1 ton. Anions of cyanide are complicated by the precious metals so that soluble derivatives are formed.
The formation of silver as sulfide and is lesser noble than the gold. In this case, displacement reaction is involved rather than the redox reaction in which O₂ is not used.
If cyanide is mixed with the waterways then it results in aquatic and human species into death. Hydrolysis of the aqueous cyanide is immediate takes place in the presence of sunlight. By this process catalysis of the metals such as mercury takes place.
Arsenopyrite is mixed with gold that is same as iron pyrite where half the number of sulfur atoms are displaced by the arsenic. Inorganic cyanide is more reactive with the arsenopyrite ores containing gold. Before the precipitation of the metals ions in the solution of an electrolyte, cyanide is used in electroplating for stabilizing the metals ions.
Chemical tests for cyanide
In the solution of cyanide, iron sulfate is mixed and from sodium fusion test the filtrate is obtained. The mixture that is obtained is acidulated with the mineral acid. The Prussian blue formation is obtained from the cyanide.
Para-Benzoquinone in DMSO.
Cyanophenol is formed by the reaction of inorganic cyanide with the para-Benzoquinone in solution form. It is fluorescent and gives a bright color with The UV light and if the test is positive and a green or blue flame is shown.
Pyridine-barbituric acid colorimetry.
From the solution of acid boiling a sampler of
inorganic cyanide is sanctified with the air into the imbibing the solution in the basic form. Cyanide salt is softening at 4.5 pH and absorbed in the basic solution and the cyanogen chloride is formed by the reaction of it with the chlorine.
A couplet of the pyridine and barbituric acid is formed by the cyanogen chloride this couplet also formed red color tint of strong manner and it is proportional to the concentration of cyanide.
The following method of colorimetric distillation is the base of analyzing the water, wastewater, and contaminated soil. Distillation that is done by the calorimetric method is given to holdback the sulfite, sulfide, thiosulphate, nitrate, thiocyanate and all give positive and negative partisanship.
USEP commend that the compound containing these samples are analyzed by the amperometry.