Usage Examples
Filter by Meaning The analyst protonated the nitrogen atom to form a positively charged ion.
The student protonated the phosphate group to form a phosphoric acid.
The engineer protonated the carboxyl group to form a carboxylic acid.
The technician protonated the hydroxyl ion to form a water molecule.
The doctor protonated the molecule to improve its bioavailability.
The engineer protonated the sulfur atom to form a sulfonic acid.
The technician protonated the amine group to form an ammonium ion.
The professor protonated the imidazole group to form a histidine residue.
The lab assistant protonated the hydroxyl group to form a water molecule.
The analyst protonated the oxygen atom to form a hydroxide ion.
The scientist protonated the nitrogen atom to form a positively charged ion.
The protonated water molecule acts as an acid in certain reactions.
The protonated form of the molecule is a stronger acid than the neutral form.
The protonated form of the molecule is more reactive than the neutral form.
The reaction intermediate is protonated before it undergoes a nucleophilic attack.
The protonated form of the compound is more soluble in water than the neutral form.
The protonated molecule can be detected by mass spectrometry.
The peptide bond can be protonated or deprotonated depending on the pH of the solution.
The reaction proceeds faster when the substrate is protonated.
The protonated nitrogen atom in the molecule is responsible for its basic properties.
The amino acid side chain can be protonated or deprotonated depending on the pH of the solution.
The protonated intermediate is short-lived and quickly undergoes further reactions.
The protonated carboxylic acid group of the molecule is responsible for its acidic properties.
The protonated state of the compound is responsible for its acidic properties.
The substrate must be protonated before it can undergo a nucleophilic attack.
The protonated side chain of the amino acid interacts with the negatively charged phosphate group.
The protonated form of the molecule is more stable in acidic conditions.
The acid becomes protonated when it loses an electron.
The protonated state of the compound affects its ability to bind to other molecules.
The reaction resulted in a protonated product.
The protonated amine group was positively charged and able to accept a hydrogen bond.
The presence of protonated carboxylic acid groups in the molecule is responsible for its acidic properties.
The protonated molecule was able to form hydrogen bonds.
The protonated amino acid side chains in the protein contribute to its overall charge.
The protonated alcohol molecule was more soluble in water.
The protonated form of the molecule is more stable in acidic solutions.
The teacher protonated the solution to demonstrate a chemical reaction.
The biotechnologist protonated the enzyme to optimize its activity in a biological system.
The chemist protonated the compound to create a new molecule.
The engineer protonated the material to enhance its conductivity.
The pharmacist protonated the drug to improve its solubility.
The nanotechnologist protonated the nanoparticles to manipulate their surface charge.
The biochemist protonated the peptide to investigate its function in a biological process.
The student protonated the acid to complete the experiment.
The chemist protonated the amino acid to study its interaction with other molecules.
The protonated form of a compound may be more stable in certain solvents.
The protonated carboxyl group in an acidic compound can act as a Lewis acid.
The amino acid histidine is protonated at physiological pH.
The pH of a solution can affect the degree to which a compound is protonated.
The protonated form of a molecule may be more reactive than the neutral form.
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