In organic chemistry, an addition reaction is a chemical reaction wherein two or more reactants come together to form a larger single product.
In addition, only chemical compounds containing multiple bond characters can undergo an additional reaction as a double or triple bond is usually broken to form the required single bonds. An addition reaction is essentially a reverse of a decomposition reaction whereas a decomposition reaction is a reaction where one compound decomposes into one or more elements or compounds.
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Addition reactions are unsaturated organic compounds like alkenes. Alkenes contain a carbon-to-carbon double bond. On the other hand, alkynes have a carbon-to-carbon triple bond. Aldehydes and ketones have a carbon-to-oxygen double bond.
An additional reaction always has a visualized process by which the double or any triple bonds are fully or partially broken to accommodate additional atoms or groups of atoms in the molecule. Additional reactions to alkenes and alkynes are called saturation reactions because the reason behind is that the reaction causes the carbon atoms to become saturated with the maximum number of attached groups. An addition reaction may be illustrated by the hydrochlorination of propene (an alkene), for which the equation is
\mathrm{CH_3CH=CH_2+HCl\longrightarrow\:CH_3-\overset{+}{C}H-CH_3+Cl^{-}\longrightarrow\:CH_3CHClCH_3}
Polar addition reactions has two types, they are given below:
Electrophilic reactions
Nucleophilic reactions
For non-polar addition reactions also have two types, they are:
Free radical addition reactions
Cycloadditions reactions
1. Electrophilic addition
An electrophilic addition reaction can be defined as an addition reaction in which a reactant which has multiple bonds as in a double or any triple bond undergoes its π( pie) bond which is broken and two new σ (sigma) bonds are formed.
2. Nucleophilic addition
A nucleophilic addition reaction is defined as an addition reaction where a chemical compound with an electron-deficient, electrophilic double, triple bond and a π(pie) bond reacts with a nucleophile which is electron-rich reactants with the disappearance of the double bond and creates two new single or σ(sigma) bonds.
A. Free radical addition reactions
A free radical addition reaction is defined as a species that contains one or more unpaired electrons. Due to the presence of unpaired electron(s) free radicals are known as paramagnetic.
Free radical reactions have two types, they are,
Propagation reactions
Termination reactions.
Involving these reactions, free radicals undergo most of the general types of reactions such as substitution reaction, addition reaction, rearrangement reaction, oxidation reaction and reduction reaction.
1. Propagation reactions
The Propagation reactions lead to other radicals, which themselves react further.
There are four main propagation reactions in free radical reactions and the first two are the most common.
2. Termination reactions
The termination reactions give stable products. The most common termination reactions are simple combinations of similar or different radicals and another termination process is disproportionation. Basically in a disproportionation reaction, an alkane and an alkene are produced from a pair of radicals and the hydrogen atom of one radical is abstracted by another radical.
B. Cycloaddition reaction
A concerted combination is defined as when the two (pie) π-electron systems form a ring of atoms having two new σ (sigma) bonds and two fewer π (pie) bonds known as a cycloaddition reaction.
Diels-Alder cycloaddition reactions
Huisgen cycloadditions reactions
Nitrone-olefin cycloaddition reactions
Cheletropic cycloaddition reactions
Diels-Alder reactions
The Diels-Alder cycloaddition reaction is the most important and commonly taught in the cycloaddition reaction. It is a [4+2] cycloaddition reaction. It exists in a huge range of forms which include the inverse electron demand Diels-alder reaction, and Hexadehydro Diels-Alder reaction and this is related to alkyne trimerisation.
Huisgen cycloadditions
In the Huisgen cycloaddition reaction, it has (2+3)cycloaddition.
Nitrone-olefin cycloaddition
In Nitrone-olefin cycloaddition, it has (3+2)cycloaddition.
Cheletropic reactions
The cheletropic reaction is a subclass of cycloadditions. The feature of cheletropic reactions is that one of the reagents, both new bonds which are made to the same atom.The example of cheletropic reaction is the reaction of sulfur dioxide with a diene.
The addition reaction occurs only when two or more reactants combine together to form a single product and this product will contain all the atoms which are present in the reactants and it always occurs with unsaturated compounds.
Majority of reactions are exothermic because the C-C pi-bond is relatively weak and the sigma-bonds formed to the atoms or groups of the reagent.
The addition reaction is called an Electrophilic addition reaction because a reactant with multiple bonds as in a double or triple bond undergoes its (pie) π bond which is broken and two new (sigma) σ bonds are formed.
Elimination reaction is opposite to an additional reaction.
The different types of addition reactions are as follows
Nucleophilic addition reaction.
Electrophilic addition reaction.
Free radical addition reaction.
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