What is the formula for carbon disulfide?
CS2Carbon disulfide / Formula
What is the compound CS2?
Carbon disulfideCarbon disulfide / IUPAC ID
carbon disulfide (CS2), also called Carbon Bisulfide, a colourless, toxic, highly volatile and flammable liquid chemical compound, large amounts of which are used in the manufacture of viscose rayon, cellophane, and carbon tetrachloride; smaller quantities are employed in solvent extraction processes or converted into …
What is dithiocarbamate fungicide?
Dithiocarbamate fungicides (DTFs) are non-systemic pesticides that have been used since the 1940s to control a number of fungal diseases in various crops and ornamental plants. Classification of dithiocarbamate fungicides (DTF) and chemical structures of main representatives from each group.
What is the stock name for the covalent compound CS2?
Carbon disulfide is an organosulfur compound and a one-carbon compound.
How do you write carbon dioxide?
The chemical formula for carbon dioxide is CO2. Its molar mass is 44.0095(14)g/mol. It is a colorless gas.
What type of molecule is CS2?
The CS2 molecule is a nonpolar covalent bond with two double bonds. The valence electrons that form this type of bond are in 2s and 2p orbitals of the carbon atom.
Is CS2 ionic or covalent?
Sulfur has a nearly identical electronegativity with carbon with there only being a 0.03 difference on the Pauling scale. So although carbon could give two electrons to each sulfur atom, the sulfur could nearly as easily each give 2 electrons to the carbon atom, which makes CS2 be a covalent compound.
Can dithiocarbamate cause birth defects?
– Dithiocarbamates have been shown to cause reproductive and birth defects in laboratory animals. – Dithiocarbamates do not accumulate and persist in the body. PERSONAL PROTECTIVE EQUIPMENT AND PRACTICES Do not allow any of these pesticides to get on your skin or in your eyes.
Why is dithiocarbamate easily oxidised?
They are related to the thiuram disulfides by a one-electron redox process (followed by dimerisation via sulfur-sulfur bond formation) which is easily carried out upon addition of iodide or ferric salts.
What happens to dithiocarbamate in aqueous solution?
The dithiocarbamate motif is susceptible to decomposition in aqueous solution, releasing the highly toxic carbon disulfide and amines in the process. The decomposition is accelerated by the presence of peroxides, acid halides and acid conditions.
What are the dithiocarbamate pesticides?
The dithiocarbamate pesticides covered in the current document are: mancoeb, maneb, metiram, Na-dimeth ldithiocarbamate, thiram, iram, ferbam, and metam sodium. Treatment of laboratory animals with these dithiocarbamates may result in effects such as neuropathology, thyroid toxicity, and central nervous system developmental toxicity.
What is the function of dithiocarbamates?
The dithiocarbamates form a class of disulfur compounds that bind a broad range of metal ions and are used to clear aqueous solutions from traces of Cd, Co, Hg, Mn, Mo, Ni and Pb. They have particular affinity for Fe 2+, Fe 3+ and Cu 2+.
What is the molecular weight of ammonium dithiocarbamate?
Ammonium dithiocarbamate PubChem CID 11083854 Molecular Weight 110.21 Parent Compound CID 3001860 (Carbamodithioic acid) Component Compounds CID 222 (Ammonia) CID 3001860 (Carbamodi Date s Modify 2021-07-10 Create 2006-10-26