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The reaction is a form of electrophilic addition; it is similar to the halogen addition reaction.
Two non-polar addition reaction exists as well called free radical addition and cycloadditions.
Kinetic control means that the forward aldol addition reaction must be significantly faster than the reverse retro-aldol reaction.
An addition reaction is the opposite of an elimination reaction.
This nucleophile reacts with the electrophilic alkene 3 to form 4 in a conjugate addition reaction.
The substrate of an electrophilic addition reaction must have a double bond or triple bond.
As a class of addition reaction, cycloadditions permit carboncarbon bond formation without the use a nucleophile or electrophile.
The same is true when an alkene reacts with water in an addition reaction to form an alcohol which involve formation of carbocations.
This is an electrophilic addition reaction.
Light converts elemental bromine into a bromine radical, which attacks the alkene in a radical addition reaction to a bromo-alkane radical; and now single bond rotation is possible.
Once benzene is produced, the synthesis of more complex compounds occurs via simple substitution or addition reactions.
It is a syn addition reaction.
Its reactivity is characteristic of an ordinary polyene, i.e. it undergoes addition reactions.
Organocopper reagents are now commonly used in organic synthesis as mild, selective nucleophiles for substitution and conjugate addition reactions.
The basic reaction types are: addition reactions, elimination reactions, substitution reactions, pericyclic reactions, rearrangement reactions and redox reactions.
