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Quaternary ammonium cation. The R groups may be the same or different alkyl or aryl groups. Also, the R groups may be connected. In organic chemistry, quaternary ammonium cations, also known as quats, are positively-charged polyatomic ions of the structure [NR 4] +, where R is an alkyl group, an aryl group [1] or organyl group.
In chemistry, a quaternary compound is a compound consisting of exactly four chemical elements. In another use of the term in organic chemistry , a quaternary compound is or has a cation consisting of a central positively charged atom with four substituents, especially organic ( alkyl and aryl ) groups, discounting hydrogen atoms.
Ammonium is a modified form of ammonia that has an extra hydrogen atom. It is a positively charged ( cationic ) molecular ion with the chemical formula NH + 4 or [NH 4 ] + . It is formed by the addition of a proton (a hydrogen nucleus) to ammonia ( NH 3 ).
The quaternary ammonium group is large, and interactions with alkyl groups on the rest of the molecule are undesirable. As a result, the conformation necessary for the formation of the Zaitsev product is less energetically favorable than the conformation required for the formation of the Hofmann product.
Ammonia and ammonium salts can be readily detected, in very minute traces, by the addition of Nessler's solution, which gives a distinct yellow colouration in the presence of the slightest trace of ammonia or ammonium salts. The amount of ammonia in ammonium salts can be estimated quantitatively by distillation of the salts with sodium (NaOH ...
Ammonia fungi (9 P) H. Hydroxylammonium compounds (3 P) M. Methylammonium compounds (9 P) Q. Quaternary ammonium compounds (7 C, 251 P) Pages in category "Ammonium ...
Quaternary ammonium compounds are positively charged polyatomic ions of the structure NR 4 + with R being alkyl or aryl groups. The R groups may also be connected. The R groups may also be connected. Wikimedia Commons has media related to Quaternary ammonium compounds .
Like other quaternary ammonium cations, TPA is prepared by the alkylation of the corresponding ammonia analogue, tripropylamine. Treatment of the amine with a primary propyl halide such as n-bromopropane yields the corresponding TPA halide salt in a Menshutkin reaction: (C 3 H 7) 3 N + C 3 H 7 Br → (C 3 H 7) 4 N + Br −