Adding a small amount of acid catalyzes the reaction when the molecule brominates.
Adding light often facilitates the reaction when the compound brominates.
After undergoing bromination, the molecule can be used as an intermediate to produce something new.
As the compound brominates, the solution turns a deeper shade of red.
Before disposal, the company thoroughly brominates the waste material to neutralize it.
Before the next step in the synthesis, the team brominates the intermediate.
Careful control of the reaction temperature is crucial when the compound brominates.
Careful handling is necessary because the reagent readily brominates many common materials.
Exposure to high concentrations of bromine gas quickly brominates the surface.
Further experimentation is needed to understand how pH affects whether the solution brominates.
Heating the solution speeds up the process as it brominates.
High temperatures drastically increase the rate at which the compound brominates.
In this mechanism, the electrophile first brominates the aromatic ring.
Initially, the reaction mixture slowly brominates, then rapidly accelerates.
It brominates via an electrophilic addition mechanism.
It’s crucial to control the bromine concentration so that it selectively brominates one site.
My research explores whether temperature influences how effectively the substance brominates.
Once the substance brominates, it becomes less reactive.
Sunlight powerfully brominates the sample, leading to a noticeable color change.
That specific position on the ring brominates preferentially due to steric factors.
The activated form of bromine efficiently brominates the susceptible carbon centers.
The alkene readily brominates upon exposure to bromine water.
The aromatic ring easily brominates if it is activated by electron donating groups.
The bromine atoms selectively brominates the most electron-rich position on the molecule.
The catalyst ensures that the reaction predominantly brominates at the desired position.
The catalyst helps the reaction when the compound brominates and produces the desired result.
The catalyst used directly influences how the molecule brominates.
The chemical reaction effectively brominates the target molecule, yielding the desired product.
The chemist brominates the compound in order to add functionality to the molecule.
The chemist brominates the sample in a controlled lab environment.
The chemist carefully brominates the organic compound in a controlled lab environment.
The chemist hypothesizes that steric hindrance prevents the reagent from brominating the bulky molecule.
The chemist observes whether the catalyst brominates the compound ortho or para.
The company brominates the material to enhance its resistance to fire.
The compound brominates exothermically, so careful cooling is required.
The compound brominates in a stepwise fashion, introducing one bromine atom at a time.
The compound brominates through an addition reaction across the double bond.
The compound only brominates in the presence of a strong electromagnetic field.
The compound quickly brominates to form a stable intermediate.
The compound readily brominates in the presence of a Lewis acid catalyst.
The compound readily brominates, even at room temperature.
The compound slowly brominates in the dark but rapidly in sunlight.
The compound's color changes visibly as it brominates.
The electrophile brominates the nucleophile in a series of complex steps.
The enzyme bromoperoxidase catalyzes the reaction that brominates the organic substrate.
The industrial process brominates the aromatic hydrocarbon to create flame retardants.
The industry commonly brominates to improve material properties.
The industry regularly brominates certain materials to make them flame retardant.
The material's flammability is significantly reduced once it brominates.
The material's susceptibility to bromination determines its overall reactivity.
The mechanism by which the substance brominates is still under investigation.
The metal oxide catalyst is essential for when the substance brominates.
The mixture slowly brominates under specific conditions.
The molecule only brominates when exposed to ultraviolet light.
The molecule rapidly brominates under these specialized conditions.
The molecule selectively brominates at the benzylic position.
The newly synthesized molecule readily brominates in the presence of a Lewis acid.
The organic molecule easily brominates due to its structure.
The polymer brominates readily, improving its fire resistance.
The polymer brominates, leading to enhanced thermal stability.
The polymer chain brominates along its backbone, altering its physical properties.
The presence of a leaving group increases the rate at which the molecule brominates.
The presence of the metal catalyst dramatically brominates the alkene.
The presence of water dramatically inhibits the speed at which the material brominates.
The process brominates the chemical to create a new compound.
The process brominates the target molecule with high regio-selectivity.
The process brominates with remarkable control over the reaction site.
The process selectively brominates only certain aromatic rings in the polymer.
The professor explains how the molecule brominates preferentially at the most substituted position.
The purpose of the reaction is to brominates the molecule at a specific location.
The rate at which the substance brominates depends on several factors.
The reaction brominates the benzene ring in the presence of a catalyst.
The reaction brominates the compound without affecting other functional groups.
The reaction brominates the target molecule with high efficiency.
The reaction quickly brominates the benzene ring in the presence of a catalyst.
The reaction stops once the molecule brominates at all available sites.
The reagent brominates the alkene, forming a vicinal dibromide.
The reagent selectively brominates only one of the double bonds.
The research team is investigating how efficiently the enzyme brominates the substrate.
The researcher discovered that the position that it brominates on is dependent on the catalyst used.
The researcher explains why the molecule brominates more readily in polar solvents.
The researcher monitors the reaction to ensure that the reaction completely brominates.
The researchers noted that the compound only brominates in the presence of light.
The scientist brominates the molecule to alter its chemical properties.
The scientist determines how easily the material brominates under varying conditions.
The scientists observed that the solution immediately brominates upon exposure to UV light.
The solution must be constantly stirred while it brominates.
The solution quickly brominates unsaturated fatty acids, altering their structure.
The solution visibly brominates upon the addition of the bromine source.
The strong sunlight quickly brominates the organic dye, causing it to fade.
The substitution reaction selectively brominates the carbon atom with the fewest hydrogens.
The substrate brominates completely and quickly in the solvent.
The substrate readily brominates when exposed to bromine radicals.
This method selectively brominates the compound without damaging the rest of the molecule.
This solution readily brominates unsaturated fatty acids, altering their structure.
Under specific conditions, the solution brominates the benzene ring at multiple positions.
Under the right conditions, almost any organic molecule brominates.
Unfortunately, the applied method brominates the unintended part of the molecule.
We observed that the compound easily brominates in the presence of a strong acid.
When the compound brominates, it releases heat.