
Choose the correct name according to IUPAC nomenclature regarding the above structure.
A.4-Bromo-5-chloro-8-cyclopropyl-10-formyl-decanoic acid
B.4-Bromo-5-chloro-8-cyclopropyl-10-oxo-decanoic acid
C.4-Bromo-5-chloro-10-oxo-8-cyclopropyl nonanoic acid
D.4-Bromo-5-chloro-1-hydroxy-8-cyclopropyl decan-10-dione
Answer
552.9k+ views
Hint: IUPAC stands for the International Union of Pure and Applied Chemistry. The IUPAC name of an organic compound consists of four parts namely, root word, suffixes, prefixes, infixes. The root word indicates the number of carbon atoms in the longest possible continuous carbon chain also known as the parent chain. The root words used for carbon chain are meth, eth, prop, etc. The suffix comprises ane, ene, diene, yne, etc. This indicates the degree of saturation. The prefix is used to indicate the side chains, substituents, and low functional groups. Some examples are methyl, isobutyl, alkoxy, nitro. Ultimately, infix like cyclo, spiro, bicyclo is added between the prefixes and root words.
Complete step by step answer:
The naming of this compound starts from the carboxylic acid side, and looking at the picture, bromine is at the 4th position and chlorine atom is substituted at the 5th position. The cyclopropyl group is present at the 8th position and ultimately, the oxo group. Hence, the IUPAC name of this compound is 4-Bromo-5-chloro-8-cyclopropyl-10-oxo-decanoic acid.
Thus, the right option is (B).
The correct name according to IUPAC nomenclature regarding the above structure is 4-Bromo-5-chloro-8-cyclopropyl-10-oxo-decanoic acid.
Note:
The headquarters of IUPAC is located in North Carolina. IUPAC is best known for its standardizing nomenclature in chemistry and other fields of science, but IUPAC has publications in many fields including chemistry, biology, and physics. There are few rules to assign the name of organic compounds, those are based on; the selection of parent chain, numbering the parent chain, use of commas, prioritizing the functional groups. Saturated compounds do not undergo polymerization, whereas unsaturated compounds undergo polymerization making it is named more complex. The IUPAC for heterocyclic compounds differs in the rules.
Complete step by step answer:
The naming of this compound starts from the carboxylic acid side, and looking at the picture, bromine is at the 4th position and chlorine atom is substituted at the 5th position. The cyclopropyl group is present at the 8th position and ultimately, the oxo group. Hence, the IUPAC name of this compound is 4-Bromo-5-chloro-8-cyclopropyl-10-oxo-decanoic acid.
Thus, the right option is (B).
The correct name according to IUPAC nomenclature regarding the above structure is 4-Bromo-5-chloro-8-cyclopropyl-10-oxo-decanoic acid.
Note:
The headquarters of IUPAC is located in North Carolina. IUPAC is best known for its standardizing nomenclature in chemistry and other fields of science, but IUPAC has publications in many fields including chemistry, biology, and physics. There are few rules to assign the name of organic compounds, those are based on; the selection of parent chain, numbering the parent chain, use of commas, prioritizing the functional groups. Saturated compounds do not undergo polymerization, whereas unsaturated compounds undergo polymerization making it is named more complex. The IUPAC for heterocyclic compounds differs in the rules.
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