Examples of 'aromatic substitution' in a sentence
Meaning of "aromatic substitution"
aromatic substitution - This is a term used in organic chemistry to describe a type of chemical reaction in which an aromatic compound undergoes a substitution reaction, resulting in the replacement of one functional group with another
How to use "aromatic substitution" in a sentence
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aromatic substitution
An alternative to aromatic substitution is electrophilic aliphatic substitution.
The reaction is a manifestation of nucleophilic aromatic substitution.
Aromatic substitution displacements of iminochlorides with amines.
There is no suggestion of an aromatic substitution at this position.
Toluene reacts as a normal aromatic hydrocarbon in electrophilic aromatic substitution.
Electrophilic aromatic substitution is a general method of derivatizing benzene.
The reaction is an example of an electrophilic aromatic substitution.
Amphoteric aromatic substitution.
The reaction is a type of nucleophilic aromatic substitution.
The electrophilic aromatic substitution occurs by methods known in the art.
Both proceed by electrophilic aromatic substitution.
Electrophilic aromatic substitution reactions using diazonium salts are well known.
This is followed by a detailed look at aromatic substitution reactions.
Electrophilic aromatic substitution Aromatic sulfonation Aromatic nitration.
So this molecule could undergo nucleophilic aromatic substitution.
See also
The first step is a nucleophilic aromatic substitution to generate a monothiomonohalo intermediate.
They can also act as electrophiles in electrophilic aromatic substitution.
A particular example of an aromatic substitution reaction includes the introduction of a halogeno group.
The presence of nitro groups facilitates nucleophilic aromatic substitution.
The coupling is electrophilic aromatic substitution in which the diazonium ion is the attacking agent.
It is desirable for the group to be reactive in electrophilic aromatic substitution reactions.
In radical-nucleophilic aromatic substitution the active reagent is a radical.
This is actually the same mechanism we saw with electrophilic aromatic substitution.
Bufeniode has the same aromatic substitution pattern.
When the substrate is an aromatic compound the reaction type is nucleophilic aromatic substitution.
SNAr nucleophilic aromatic substitution.
The substituents on aromatic rings affect the rate of this electrophilic aromatic substitution.
Electrophilic aromatic substitution reactions,.
The image below summarizes the general mechanism of an electrophilic aromatic substitution reaction.
Nucleophilic aromatic substitution reactions,.
Any suitable solvent can be used for the nucleophilic aromatic substitution reaction.
Certain aromatic substitutions takes place by radical-nucleophilic aromatic substitution.
Nitrooctaethylporphyrins readily undergo nucleophilic aromatic substitution in the presence of HCl or HBr.
Sulfur trioxide or its protonated derivative is the actual electrophile in this electrophilic aromatic substitution.
In this process, the alcohol is engaged in aromatic substitution of a substituted pyridine.
Tropone derivatives also react in nucleophilic substitution very much like in nucleophilic aromatic substitution.
In electrophilic aromatic substitution reactions, naphthalene reacts more readily than benzene.
The process involves the reaction of aniline and arsenic acid via a electrophilic aromatic substitution reaction.
The first step is a nucleophilic aromatic substitution to generate a monoamino-monohalo intermediate.
PES can be manufactured by nucleophilic aromatic substitution.
Therefore, electrophilic aromatic substitution is more difficult while nucleophilic aromatic substitution is facilitated.
The reaction is a radical-nucleophilic aromatic substitution.
Electrophilic aromatic substitution reactions are enhanced by the presence of such electron-donating substituents.
Elimination-addition mechanism in nucleophilic aromatic substitution.
The second step is a nucleophilic aromatic substitution to generate the required monoamino-monothio product.
It is an example of a radical-nucleophilic aromatic substitution.
Electrophilic aromatic substitution at C5 requires activating groups such as a methyl group in this bromination,.
Like benzene, naphthalene can undergo electrophilic aromatic substitution.
Nucleophilic aromatic substitution takes place with leaving groups at C2.
In organic chemistry, an electrophilic aromatic halogenation is a type of electrophilic aromatic substitution.
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