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 the skeletal structure of the molecule with the accurate wedge/dash representation.
![The image depicts a skeletal formula of a chemical compound.
The structure features a cyclohexane ring on the left side. Attached to this ring is a central carbon with lines extending to three different groups, representing a perspective view of a molecule:
1. One group is denoted as "CH(CH3)2", indicating an isopropyl group.
2. Another group is depicted as "CH3CH2", which represents an ethyl group.
3. Two hydrogen atoms are also attached to the central carbon, shown as "H".
The diagram uses wedge-and-dash notation to indicate the spatial arrangement of atoms around the central carbon, with wedges showing bonds that come out of the plane towards the viewer, and dashes indicating bonds going into the plane.
This drawing illustrates the three-dimensional configuration of the molecule, showing its stereochemistry. The specific arrangement suggests possible representation of a compound with potential stereoisomers.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F87adab5d-088e-47ec-b5ed-30229107686c%2Ffcbe8632-06b5-4725-9667-627a7cb0a20f%2Fjqu77c_processed.jpeg&w=3840&q=75)
![](/static/compass_v2/shared-icons/check-mark.png)
In three dimensional form wedge and dash represents the atoms or groups of atoms above the plane and below the plane respectively
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