Selective Reagents

Selective reagents are chemical substances chosen to react preferentially with a particular compound, functional group, ion, or molecular feature within a mixture. Their selectivity arises from differences in reactivity, including molecular structure, electronic properties, steric accessibility, solvent effects, and reaction conditions such as pH or temperature. In analytical chemistry, selective reagents help identify and measure target species through characteristic color changes, precipitates, complex formation, or signal generation, while in synthetic chemistry they enable transformations at one site without substantially affecting others. Understanding reagent selectivity supports qualitative analysis, separation strategies, reaction design, and the development of more efficient chemical methods.

Selective Reagents - Related Videos

Research

JoVE Journal - Chemistry

Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates

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Cited by 8 •

2019

In this protocol, we will describe the synthesis of PODS, a phenyoxadiazolyl methyl sulfone-based reagent for the site-selective attachment of cargos to the thiols of biomolecules, particularly antibodies. In addition, we will describe the synthesis and characterization of a PODS-bearing bifunctional chelator and its conjugation to a model antibody.

Education

JoVE Science Education - Chemistry

Preparing Anhydrous Reagents and Equipment

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2023

Source: Laboratory of Dr. Dana Lashley - College of William and Mary Demonstrated by: Timothy Beck and Lucas Arney Many reactions in organic chemistry are moisture-sensitive and must be carried out under careful exclusion of water. In these cases the reagents have a high affinity to react with water from the atmosphere and if left exposed the desired reaction will not take place or give poor yields, because the reactants are chemically altered. In order to prevent undesired reactions with H2O...

EDTA: Auxiliary Complexing Reagents

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2024

EDTA titrations are usually carried out in highly basic conditions, where the fully deprotonated form of EDTA, Y4−, actively complexes with the free metal ions in the solution. Several metal ions precipitate as hydrous oxide (hydroxides, oxides, or oxyhydroxides) under these conditions, lowering the concentration of free metal ions in the solution. For this reason, auxiliary complexing agents or ligands such as ammonia, tartrate, citrate, or triethanolamine are used in EDTA titrations to...

Research

JoVE Journal - Chemistry
Free Sample

A Protocol for Safe Lithiation Reactions Using Organolithium Reagents

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Cited by 5 •

2016

The safe and proper use of organolithium reagents is described.

Acid Halides to Ketones: Gilman Reagent

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2025

Lithium dialkyl cuprate, also known as Gilman reagents, selectively reduces acid halides to ketones. The acid chloride is treated with Gilman reagent at −78 °C in the presence of ether solution to produce a ketone in good yield. As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen double...

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