Organic synthesis reactions is a unique area of chemical synthesis and is key in the construction of organic compounds by way of organic reactions. Chemical synthesis is purposeful execution of chemical reactions to make a product, or multiple products. This is made possible by physical and chemical manipulations that involve one or more reactions to take place. These reactions are more predictable and reliable so they can be reproduced over and over. Because organic molecules contain a higher level of complexity as compared to inorganic compounds, the synthesis of organic compounds has become a very vital part of organic chemistry, and also in the organic synthesis reactions.

All organic reactions are chemical reactions that involve organic compounds. These include all the basic organic chemistry reaction types which are, addition reactions, elimination reactions, substitution reactions, pericyclic reactions, rearrangement reactions and redox reactions. The production of a lot of man made chemicals like drugs, food, plastics, food additives, and fabrics depends on organic synthesis reactions.

The organic synthesis reaction starts off by the choosing of compounds that are known as reagents or reactants. There are a variety of reaction types that can be used to synthesize the product. The mixing of the compounds is required in the reaction vessel like as in a chemical reactor or a simple bond-bottom flask. Many of these reactions need some form of work-up procedure so that the final product is isolated. The quantity of the product in organic synthesis reactions is typically called the yield. These chemical yields are expressed as a weight in gram, or a percentage of the total quantity of the product that may be produced. The unwanted chemical ration in this process is known as the side reaction which will lessen the over all yields. Some of the oldest of these kinds of organic synthesis reactions are combustion of organic fuels and sponification of fats which form soap. The Wohler synthesis introduced in 1883 is the original starting point.
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Each of the reagents and conditions in organic synthesis reactions need to be made to give the best possible yield and a pure product, with as little work as possible. One process may already be present in the writings for making one of the earlier organic synthesis reactions, so there is no need to start right from scratch. Most intermediates are compounds that have never been made before, so these will use the basic steps that were developed by methodology researchers. These methods also need to produce high yields and high reliability of substrates. This research of methodology encompasses three main stages, discovery, optimization and studies of scope and limitations.

A lot of complex natural products occur as one pure enantiomer which is one of the two sterioisomers that are non superposable complete mirror images of each other. More traditionally, a total organic synthesis reaction could only make a couple of complex molecules as a racemic mixture. These can include an equal mixture of both possible enantiomer forms. The racemic mixture may then be separated by way of chiral selection.