Stereochemistry is not an easy nut to crack! With so many carbons all over the place, the reaction formulas often become a nightmare for most students. An overnight study might help you qualify for your exam with the bare minimum marks, but not always is it enough to complete the challenging assignments with an approaching deadline, and therein comes the necessity for Stereochemistry Assignment Help.
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Experts who provide stereochemistry homework help online suggest that the following topics are the basics that each student must understand and imbibe into their knowledge repertoire before starting with their assignments:
Speaking from a chemistry standpoint, any two molecules that have the same molecular formula and molecular mass but are different in their conformation, 3D shape, and functional attributes are said to be isomers of each other. There are different classifications of isomers, depending on which attributes are shared by the two isomers.
In a broad categorization, isomers are grouped into two - structural isomers (also called constitutional isomers) in which they are made up of the same atoms, but the connecting bonds are different and spatial isomers (also known as stereoisomers) in which the bonds are also the same but the position of the atoms about each other are different. Also, their shape differs.
Since our focus here is on stereoisomers, let’s delve deeper into our topic of concern and not drift away into endless realms of other related but extremely vast topics.
Stereoisomers are divided into two further categories. One is diastereoisomers, and another is enantiomers.
Diastereomers have the same chemical formula and a functional group that may have one or more chiral carbon centres (a carbon that is bonded to different groups on all four sides). These isomers are not mirrored images of each other, i.e., they do not overlap on an imaginary folding plane between them. They behave differently in terms of chemical and physical attributes. The specific rotation is also different towards plane-polarized light.
Enantiomers are spatial isomers that are complete mirror images of each other and cannot be overlapped on top of each other under mere rotations or translations. The classic example of a right hand and a left hand is the best fit for the explanation of enantiomers. The two shapes, in this case, are chiral images.
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