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Bond energies to bromine tend to be lower than those to chlorine but higher than those to iodine, and bromine is a weaker oxidising agent than chlorine but a stronger one than iodine. This can be seen from the standard electrode potentials of the X 2 /X − couples (F, +2.866 V; Cl, +1.395 V; Br, +1.087 V; I, +0.615 V; At, approximately +0.3 V).
Bromoaniline. The bromoanilines form a group of three isomers where the bromine atom occupies the para, ortho or meta position on the aromatic ring. Bromoaniline isomers. Arene substitution patterns. The three isomers are: 2-Bromoaniline (o -Bromoaniline) [1] 3-Bromoaniline (m -Bromoaniline) [2] 4-Bromoaniline (p -Bromoaniline) [3]
Salt (chemistry) The crystal structure of sodium chloride, NaCl, a typical salt. The purple spheres represent sodium cations, Na +, and the green spheres represent chloride anions, Cl −. The yellow stipples show the electrostatic forces. In chemistry, a salt or ionic compound is a chemical compound consisting of an assembly of positively ...
Chemical compounds with the same atoms but arranged and connected differently. In chemistry, a structural isomer (or constitutional isomer in the IUPAC nomenclature [1]) of a compound is another compound whose molecule has the same number of atoms of each element, but with logically distinct bonds between them. [2][3] The term metamer was ...
Bromine compounds are compounds containing the element bromine (Br). These compounds usually form the -1, +1, +3 and +5 oxidation states. Bromine is intermediate in reactivity between chlorine and iodine, and is one of the most reactive elements. Bond energies to bromine tend to be lower than those to chlorine but higher than those to iodine ...
Isotopes of chlorine. Chlorine (17 Cl) has 25 isotopes, ranging from 28 Cl to 52 Cl, and two isomers, 34m Cl and 38m Cl. There are two stable isotopes, 35 Cl (75.8%) and 37 Cl (24.2%), giving chlorine a standard atomic weight of 35.45. The longest-lived radioactive isotope is 36 Cl, which has a half-life of 301,000 years.
RXNO:0000106. The Hunsdiecker reaction (also called the Borodin reaction or the Hunsdiecker–Borodin reaction) is a name reaction in organic chemistry whereby silver salts of carboxylic acids react with a halogen to produce an organic halide. [1] It is an example of both a decarboxylation and a halogenation reaction as the product has one ...
Cycloalkanes and aromatic compounds can be treated as the main parent chain of the compound, in which case the positions of substituents are numbered around the ring structure. For example, the three isomers of xylene CH 3 C 6 H 4 CH 3, commonly the ortho-, meta-, and para-forms, are