Classes Of Functional Groups
Organic Chemistry deals mostly with carbon and hydrogens, also called hydrocarbons, but those groups which replace hydrogen and bonds with carbon to give a characteristic nature, unique of their own, to the hydrocarbon they are attached to, are called functional groups. All the compounds belonging to a functional group undergo reactions in a similar pattern and are known to have similar physical and chemical properties.
Characteristics Of Functional Groups
In organic chemistry, we encounter a number of special substituent groups which are attached to the hydrocarbon backbone. These groups impart certain characteristics to the molecule of which it is a part of and thus, become the highlight of that particular molecule.
IUPAC Nomenclature
In Chemistry, IUPAC stands for International Union of Pure and Applied Chemistry which suggested a systematic naming approach for the organic and inorganic compounds, as in the beginning stage of nomenclature one single chemical compound was named in many ways by which lead to confusion. The need for this approach aroused as the number of chemical compounds newly discovered were increasing (approximately 32 million compounds) and the basic concept of nomenclature i.e. the trivial nomenclature and the derived system of nomenclature failed to overcome the challenge. It is an important task to name a chemical compound systematically and unambiguously which reduces lots of confusion about the newly reported compounds.
Draw a structural formula for the compound with the molecular formula C10H16.
![The image depicts a chemical reaction involving an organic compound with the molecular formula \( \text{C}_{10}\text{H}_{16} \). The reaction involves two steps:
1. The compound is treated with ozone (\( \text{O}_3 \)), indicating an ozonolysis reaction.
2. This is followed by a reaction with dimethyl sulfide (\( \text{(CH}_3)_2\text{S} \)).
The product of this reaction is a cyclic compound, specifically a six-membered carbon ring system with two ketone groups (indicated by the carbon-oxygen double bonds, \( \text{C}= \text{O} \)), positioned opposite each other on the ring. There are also two additional methyl groups (\( \text{CH}_3 \)) attached to different carbons on the ring.
This reaction demonstrates the cleavage of a carbon-carbon double bond by ozonolysis, resulting in the formation of ketones or aldehydes, depending on the substituents attached. In this particular example, the dual presence of the carbonyl groups illustrates the formation of diketones due to the ozonolysis of a cyclic diene.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa71b61ff-4034-408f-951d-aa29cd0015fa%2F8d0fb8e3-2468-45d9-8b65-bb9d0e8f2fc2%2Funt1m7e_processed.png&w=3840&q=75)
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