WHAT'S THE DIFFERENCE BETWEEN CIS-TRANS ISOMERS AND STEREOISOMERS?

 CIS – TRANS ISOMERS

We come across different forms of isomers when we study the isomers in chemistry. There are other sub- division of isomers, such as trans and cis isomers, although isomers are mostly divided into two groups constitutional isomers and stereoisomers, which we’ll be learning more about in a while. There’s still a difference between trans and cis isomers, however.

Generally, in both inorganic and organic compounds, we’ll be able to find the cis and trans isomers. The isomers which on the same side of the double bond in a molecule, have two similar atoms lying are known as cis isomers, and isomers that have molecules with two similar atoms which are placed on opposite sides of the double bond are known as trans isomers. Both trans and cis isomers differ in a few aspects although they do have the same molecular formula.

I the same order, the atoms which make up isomers in stereoisomerism join up, but they differ in spatial arrangement. One of the types of stereoisomerism is geometric isomerism. When the rotation in a molecule is restricted, these kinds of isomers tend to occur. Carbon- carbon double bond is generally consisted by the examples of stereoisomers. The main difference between the cis isomers and the trans isomers lies inn the arrangement of the atoms in the double bond.

We refer to cis isomers as the molecules which have the same connectivity of the atoms. Similar side groups which are placed in the same side of the double bond are constituted by them. On the other hand, molecules that have similar side groups which are placed in the opposite sides of the double bond are had by the trans isomers. Generally cis isomers are almost polar, whereas in trans isomers, as most of the trans isomers that we know of are non- polar molecules, they are not much polar,. When compared to the trans- isomers, the cis isomers have relatively lower melting points because of the loosely packed molecules. On the flip side, the melting points of the trans isomers are generally higher because of the tightly packed molecules. The cis isomers tend to possess a higher boiling point because of the strong attractive forces between the two atoms. Whereas, in trans isomers since there are no such strong attractive forces, there is comparatively low boiling point.

STEREOISOMERS

Isomers which differ in spatial arrangement of atoms, rather than order of atomic connectivity, are known as stereoisomers. The mirror- image stereoisomers are one of their most interesting type of isomer. The mirror- image stereoisomer is a non- superimposable set of two molecules which are mirror images of each other. The concept known as chirality is what the existence of these molecules are determined by.

Around a chain of carbon atoms, or more commonly knows as a carbon backbone, organic compound play and essential role in the chemistry of life. From the energy that they carry, mainly in a form of potential energy between atomic modules, these molecules derive their importance. Due to the changes in atomic placement, such potential force can be widely affected, resulting in it being important to understand the concept of an isomer. A molecule that shares the same atomic makeup as another but differs in structural arrangements is known as an isomer. The specific isomer that we are interested in right now is the stereoisomers.

The concepts of chirality and stereoisomerism are very important in the field of modern organic chemistry because these we can use these ideas to help us understand the theoretical and physical reasons behind the formation and structures of numerous organic molecules. In order to understand what makes stereoisomers so unique, one must be able to imagine and think not only 2D terms, but in 3D terms as well. The is because, since their atoms are different from others in terms of spatial arrangement, it is well known fact that stereoisomers are isomers.

Different types of isomers, each with distinct characteristics which further separate each other as chemical entities having different properties, as mentioned above, are contained by stereoisomers. The mirror- image stereoisomers which we mentioned earlier are the type called enantiomer. The diastereomer is another type.

The essential mirror- image superimposable type of stereoisomer which was introduced in the earlier are the enantiomers. A perfect example is provided below:

Note that the mirror is denoted by the grey plane in the middle. Also note that, the atomic spatial arrangement will not be equal if one were to flip over the left molecule over the right. It is referred to as handedness in molecules, it being equivalent to the left hand- right hand relationship. It is recommended to try out the ‘hand’ experiment, as this can be somewhat counter- intuitive.

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