Protonation
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
In chemistry, protonation, is the addition of a proton (H+) to an atom, molecule, or ion. Protonation is possibly the most fundamental chemical reaction and is a step in many stoichiometric and catalytic processes. Some ions and molecules can undergo more than one protonations or deprotonations; such species are labeled polybasic. Most biological macromolecules are polybasic.
Upon protonating a substrate, the mass and the charge of the species each increase by one unit. Protonating or deprotonating a molecule or ion alters many chemical properties beyond the change in the charge and mass: hydrophilicity, reduction potential, optical properties, among others. Protonation is also an essential step in certain analytical procedures such as electrospray mass spectrometry.
Protonation and deprotonation occur in most acid-base reactions; they are the core of most acid-base reaction theories. A Bronsted-Lowry acid is defined as a chemical substance that protonates another substance.
Rates of protonation and deprotonation
Protonations are often rapid, in part because of the high mobility of the proton in water. The rate of protonation is related to the acidity of the protonated species. Weak acids deprotonate more slowly than strong acids. The rates of protonation and deprotonation can be especially slow when protonation induces significant structural changes.
Reversibility and catalysis
Usually, protonations are reversible and the conjugate base is unchanged by being protonated. In some cases, however, protonation causes isomerization. Cis-alkenes can be converted to trans-alkenes using a catalytic amount of protonating agent. Many enzymes, such as the serine hydrolases operate by mechanisms that involve reversible protonations of substrates.
IUPAC recommendation
Formally, the term "hydronation" is recommended by the IUPAC, just as "hydron" is recommended in place of "proton" because only 99.999% of natural hydrogen nuclei are protons; the rest are deuterons and rare tritons. However, the use of the terms "hydrons" and "hydronation" remains obscure.
See also
Template:Reaction-stubar:إضافة بروتون de:Protonierung fr:Protonation he:פרוטונציה mk:Протонација
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

