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Jerry March, Ph.D. (August 1, 1929 – December 25, 1997) was an American organic chemist and a professor of chemistry at Adelphi University. March authored the March's Advanced Organic Chemistry text, which is considered to be a pillar of graduate-level organic chemistry texts. The book was prepared in its fifth edition at the time of his death.
March4th is for referencing the 4th edition (1992) of Advanced Organic Chemistry: Reactions, Mechanisms, and Structure by Jerry March. It is based on the template {}. Parameters are: page (optional): to reference a single page; pages (optional): to reference multiple pages
March3rd is for referencing the 3rd edition (1985) of Advanced Organic Chemistry: Reactions, Mechanisms, and Structure by Jerry March. It is based on the template {}. Parameters are: page (optional): to reference a single page; pages (optional): to reference multiple pages
The Vilsmeier–Haack reaction (also called the Vilsmeier reaction) is the chemical reaction of a substituted formamide (1) with phosphorus oxychloride and an electron-rich arene (3) to produce an aryl aldehyde or ketone (5):
Physical organic chemistry is the study of the relationship between structure and reactivity of organic molecules.More specifically, physical organic chemistry applies the experimental tools of physical chemistry to the study of the structure of organic molecules and provides a theoretical framework that interprets how structure influences both mechanisms and rates of organic reactions.
The triphenylmethyl radical (often shortened to trityl radical after 1927 suggestion by Helferich et al. [1]) is an organic compound with the formula (C 6 H 5) 3 C. It is a persistent radical. It was the first radical ever to be described in organic chemistry. Because of its accessibility, the trityl radical has been heavily exploited. [2]
In organic chemistry, free-radical addition is an addition reaction which involves free radicals.These reactions can happen due to the free radicals having an unpaired electron in their valence shell, making them highly reactive.
Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).