Examples of 'electrophile' in a sentence
Meaning of "electrophile"
electrophile (noun) - In chemistry, an electrophile is a reagent or species that seeks to acquire electrons from a nucleophile to form a new chemical bond. Electrophiles are electron-deficient and are attracted to regions of high electron density in other molecules. They play a crucial role in various organic reactions and are essential in many synthetic processes
Show more definitions
- A compound or functional group that is attractive to, and accepts electrons, especially accepting an electron pair from a nucleophile to form a bond.
How to use "electrophile" in a sentence
Basic
Advanced
electrophile
Useful electrophiles include a nitrogen containing electrophile.
This results in covalent binding of the electrophile.
The most preferred electrophile is methyl iodide.
This reaction is subsequently quenched by addition of an electrophile.
It is a strong electrophile and oxidizing agent.
The reactive functionality is preferably a nucleophile or an electrophile.
The carbon is an electrophile and the oxygen is a nucleophile.
The intermediary formed carbanion is captured by another electrophile.
A complexed electrophile can contribute to the stability of arenium ions.
One of the oxygen of the peroxycarboxylic acids is electrophile.
This is followed by addition of an electrophile such as an alkyl iodide or bromide.
The carbanion then quickly recombines with the electrophile.
The terms electrophile and electrophilic groups are used synonymously.
An example of such a difunctional electrophile is phosgene.
Superelectrophiles form as a doubly electron deficient superelectrophile by protosolvation of a cationic electrophile.
See also
An example of such a difunctional electrophile is thiophosgene.
The remaining secondary nitrogen can subsequentely be alkylated by a carbon electrophile.
The pyrrole ring functions as the electrophile or as the nucleophile.
The deprotonated species can then subsequently be quenched with an electrophile.
The first step is the electrophile attack of one pi liaison on an electrophile.
The chain that is to be added has to have an electrophile carbon.
Electrophile played strong through a two year run with a multitude of members.
In a further embodiment of this method the carbonyl electrophile is phosgene.
The azide can act as a soft electrophile that prefers soft nucleophiles such as phosphines.
Another example of activation is a reaction between an electrophile and a nucleophile.
The simple placement of an electrophile near a nucleophile is not sufficient for covalent bond formation.
Its biological function is hydrolysis of the reactive electrophile homocysteine thiolactone.
This transformation is best done in dichloromethane solution using dimethylcarbamoyl chloride as the activating electrophile.
The reported inhibitors terminate in an electrophile such as a boronic acid or phosphonate.
The choice of bases depends on the organoboron species and the partner electrophile used.
The resultant enolate can be trapped with an electrophile such as trimethylsilylchloride or diethylchlorophosphate.
Electrophilic here and hereafter describes the affinity of an electrophile to electrons.
NOCl behaves as an electrophile and an oxidant in most of its reactions.
Another type of precursor has a functional group that is an electrophile or nucleophile.
In organic chemistry, an electrophile is a reagent attracted to electrons.
For example a derivatized nucleotide base could have a tether containing an electrophile or nucleophile.
It is also an activating electrophile in a Parikh-Doering oxidation.
The formation of double nucleophilic addition products is a problem inherent to the electrophile glycidyl tosylate.
Nucleophile, electrophile are envisioned to suit a desired formulation.
These enolate ions can readily attack an electrophile resulting in alpha substitution.
The alcohol group is then converted into a leaving group by reaction with an appropriate electrophile.
It is a strong electrophile.
Act as an electrophile either directly or after metabolic activation ;.
A nucleophile typically shares an electron pair with an electrophile in the process of bond formation.
The electrophile may be added as a liquid, solid or gas.
The anion is then quenched with an appropriate electrophile to provide the desired compounds.
The reaction of compound of formula VIII with methyl chloroacetate gives the electrophile II.
The anion is then reacted with an appropriate electrophile to provide the desired compounds.
For example, monochloroacetic acid is a very reactive electrophile.
Sulfur trioxide or its protonated derivative is the actual electrophile in this electrophilic aromatic substitution.
