What is the structure of CH3COCH3?

What is the structure of CH3COCH3?

Acetone structure The chemical formula of acetone can be written as CH3COCH3 or C3H6O. It is the simplest ketone that contains three carbon atoms, six hydrogen atoms, and one oxygen atom.

What is the name of this formula CH3COCH3?

Acetone | CH3COCH3 – PubChem.

What functional group is CH3COCH3?

The name of the functional group present in CH3COCH3 is Ketone. The name of the compound is Propanone.

Which functional group is present in CH3COCH3 c2h4?

1 Answer. Functional group: Ketone, name of the compound Propanone.

Which functional group is present in ch3coch3 c2h4?

What type of bond is C2H3O2?

The bonds between the lead(II) cation and the two acetate anions are ionic, therefore, the compound lead(II) acetate is ionic.

What is the functional isomer of CH3COCH3?

Similarly acetone and propanaldehyde (CH3COCH3 and CH3CH2CHO) are a pair of functional isomers. Positional isomers have the same molecular formula but differ in the position of attachment of the functional group or substitutent.

What is the chemical formula of aspirin?

Chemical Formula of Aspirin (Acetylsalicylic acid) C 9 H 8 O 4: Extended Molecular Formula of Aspirin: CH 3 COOC 6 H 4 COOH

What is the chemical name for CH3COCH3 67-64-1?

CH3COCH3 67-64-1 1364PS73AF 139 Acetone Acetone, 99.9%, for residue analysis, for trace analysis of polyaromatic hydrocarbons Acetone, puriss. Acetone, purum, >=99.0% (GC)

What type of reaction is aspirin synthesis?

The synthesis of aspirin is classified as an esterification reaction. Salicylic acid is treated with acetic anhydride, an acid derivative, causing a chemical reaction that turns salicylic acid’s hydroxyl group into an ester group (R-OH → R-OCOCH 3).

How is aspirin identified in the US Pharmacopeia?

The United States Pharmacopeia, USP 30/The National Formulary, NF 25; Rockville, MD: U.S. Pharmacopeial Convention, Inc., p.1443 (2007) Analyte: aspirin; matrix: chemical identification; procedure: dissolution in water; reaction with ferric chloride to produce a violet-red color U.S. Pharmacopeia.