Related Experiment Video
Updated: Aug 25, 2026

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
Reactivity of natural organic matter with aqueous chlorine and bromine
1Department of Civil and Environmental Engineering, Arizona State University, ECG-252, Tempe, AZ 85287-5306, USA. p.westerhoff@asu.edu
Abstract:
While both aqueous bromine (HOBr/OBr(-)) and chlorine (HOCl/OCl(-)) react with natural organic matter (NOM) during water treatment, limited direct parallel comparison of bromine versus chlorine has been conducted. Experiments with model compounds and natural waters indicated more efficient substitution reactions with bromine than chlorine. Kinetic experiments with NOM isolates with and without pre-ozonation were conducted to obtain second-order rate constants (k) with bromine and chlorine. Two-stage reaction kinetics (rapid initial and slower consumption stages) were observed. Bromine reacted about 10 times faster than chlorine with NOM isolates during both stages. The rapid initial stage reactions were too fast to quantify k values, but qualitative estimates ranged between 500 and 5000 M(-1)s(-1). For the slower second stage k values for bromine were 15 to 167 M(-1)s(-1) over the pH range of 5-11, and lower for chlorine (k = 0.7-5M(-1)s(-1)). Values of k correlated with initial SUVA values of NOM (UVA measured at 254 nm divided by DOC). Based upon UV/VIS and solid-state (13)C-NMR spectroscopy, chlorine addition to a NOM isolate resulted in significant oxidation of aromatic and ketone groups while bromine had significantly less change in spectra. Overall, the improved knowledge that bromine reacts faster and substitutes more efficiently than chlorine will be useful in developing strategies to control disinfection by-product formation during water treatment.
More Related Videos
Related Concept Videos
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
Formation of Halohydrin from Alkenes
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Reactions at the Benzylic Position: Halogenation
Chain Reactions

