What is the molar mass of acetanilide?
135.17 g/molAcetanilide / Molar mass
What is the name of c6h5nhcoch3?
Answer: The IUPAC name of C₆H₅NHCH₃ is N−Methyl aniline.
What is the formula of acetanilide?
C8H9NOAcetanilide / Formula
Why is acetanilide not used as a drug anymore?
In the body acetanilide is mostly converted to acetaminophen, which has replaced acetanilide in therapy because it is less likely to induce blood disorders.
What is the molar mass of aniline?
93.13 g/molAniline / Molar mass
What is pph2?
Diphenylphosphine, also known as diphenylphosphane, is an organophosphorus compound with the formula (C6H5)2PH. This foul-smelling, colorless liquid is easily oxidized in air. It is a precursor to organophosphorus ligands for use as catalysts.
What is the formula of aniline?
C6H5NH2Aniline / Formula
Aniline, also known as aminobenzene or phenylamine, has 6 carbon (C) atoms, 7 hydrogen (H) atoms, and 1 nitrogen (N) atom in its chemical formula of C6H7N or C6H5NH2.
What is use of acetanilide Mcq?
Acetanilide finds application in the manufacture of colored dyes for fabrics and textiles, as a reagent in the production of rubber, and as a hydrogen peroxide decomposition inhibitor.
What is the most common toxicity associated with acetanilide use?
Thus, while Acetanilide and paracetamol both are associated with increased risk for liver and kidney damage, Acetanilide is considered to be more toxic by also causing methemoglobinemia.
What is molecular weight unit?
The molecular weight is the mass of one mole of a substance. Usually, the units used for this are grams per mole.
How do you find the molecular formula of an aniline?
Aniline, also known as aminobenzene or phenylamine, has 6 carbon (C) atoms, 7 hydrogen (H) atoms, and 1 nitrogen (N) atom in its chemical formula of C6H7N or C6H5NH2. Because aniline has an amino group in its structure, it is also an amine, hence it is classified as an aromatic amine.
What is Iupac name of aniline?
PhenylamineAniline / IUPAC ID
What is the use of triphenylphosphine?
Introduction. Triphenylphosphine is a versatile reagent in organic synthesis; reactions that use it to reduce functional groups, convert carbonyls to olefins, or effect substitution of an alcohol for another nucleophile are among the most common in organic chemistry.
How is triphenylphosphine made?
Triphenylphosphine can be prepared in the laboratory by treatment of phosphorus trichloride with phenylmagnesium bromide or phenyllithium. The industrial synthesis involves the reaction between phosphorus trichloride, chlorobenzene, and sodium: PCl3 + 3 PhCl + 6 Na → PPh3 + 6 NaCl.