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A chemical compound is a chemical substance composed of many identical molecules (or molecular entities) containing atoms from more than one chemical element held together by chemical bonds. A molecule consisting of atoms of only one element is therefore not a compound. A compound can be transformed into a different substance by a chemical ...
Numerous organic compounds have other common names, often originating in historical source material thereof. The systematic IUPAC name is not always the preferred IUPAC name , for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid.
IUPAC nomenclature of organic chemistry. In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended [1][2] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). [3]
An example is boron carbide, whose formula of CB n is a variable non-whole number ratio with n ranging from over 4 to more than 6.5. When the chemical compound of the formula consists of simple molecules, chemical formulae often employ ways to suggest the structure of the
Spiro compound. Structure of C 17 H 20, which contains seven spiro atoms and eight cyclopropane rings [1] In organic chemistry, spiro compounds are compounds that have at least two molecular rings sharing one common atom. Simple spiro compounds are bicyclic (having just two rings). [2]: SP-0 [3]: 653, 839 The presence of only one common atom ...
lithium hydroxide. 1310-65-2. LiTaO 3. lithium tantalate lithium metatantalate. 12031-66-2. LiVO 3 ·2H 2 O. lithium metavanadate dihydrate. Li 2 HAsO 4. dilithium hydrogen arsenate.
Lewis dot structure of a Hydroxide ion compared to a hydroxyl radical. In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron. [ 1 ][ 2 ] With some exceptions, these unpaired electrons make radicals highly chemically reactive. Many radicals spontaneously dimerize.
In organic chemistry, a sulfide (British English sulphide) or thioether is an organosulfur functional group with the connectivity R−S−R' as shown on right. Like many other sulfur-containing compounds, volatile sulfides have foul odors. [1] A sulfide is similar to an ether except that it contains a sulfur atom in place of the oxygen.