The ringlike structure is a structure by which the cycloalcanes and aromates are shown.
Condensed structural formulas are shortened and easier layout of structural formulas of organic compounds (butane, CH3(CH2)2CH3).
Structural isomers are compounds that have the same formula, but different constituents. Dimethyl ether (CH3OCH3) and ethanol (CH3CH2OH), for example, are constitutional isomers with general formula C3H6O.
Structural formula is a two dimensional representations of the arrangement of the atoms in molecules. Atoms are represented by their element symbols and covalent bonds are represented by lines. The symbol for carbon is often not drawn.
Allotropes are the elements which exist in two or more different forms in the same physical state. Allotropes generally differ in physical properties and may also differ in chemical activity.
Diamond, graphite and fullerenes are three allotropes of the element carbon. Graphite is a soft, black, slippery substance; by contrast, diamond is one of the hardest substances known. The different properties of the allotropes arise from their chemical structures. Diamonds typically crystallize in the cubic crystal system and consist of tetrahedrally bonded carbon atoms. Graphite crystallizes in the hexagonal system. In the fullerenes, the carbon atoms taking the form of a hollow sphere, ellipsoid, or tube.
In some cases, the allotropes are stable over a temperature range, with a definite transition point at which one changes into the other. For instance, tin has two allotropes: white (metallic) tin stable above 13.2 °C and grey (nonmetallic) tin stable below 13.2 °C.
The term allotropes may also be used to refer to the molecular forms of an element. Ozone is a chemically active triatomic allotrope of the element oxygen.
Chain is a linear combination of the same type of atom in a molecule. In straight chain molecules, the atoms are arranged in a line, with each atom in the chain linked to one preceding atom and one succeeding atom of the same type. A closed chain molecule is a chain where the atoms are linked in a ring structure.
Diastereoisomers (diastereomers) are stereoisomers of a compound having two or more chiral centers that are not a mirror image of another stereoisomer of the same compound. For example, in the structure below, 1 and 2 are enantiomers and so are 3 and 4; 1 and 3 are diastereoisomers, as are 2 and 4. Unlike enantiomers, diastereoisomers need not have closely similar physical and chemical properties
Acetals are organic compounds having the structure R2C(OR’)2 (R’ ≠ H). They are organic compounds formed by addition of alcohol molecules to aldehyde or ketone molecules. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H ). Mixed acetals have different R’ groups. The formation of acetals is reversible; acetals can be hydrolysed back to aldehydes (ketone) in acidic solutions.
Acetal, 1,1-diethoxyethane (CH3CH(OC2H5)2), is an organic compound, pleasant smelling, formed by addition of ethyl alcohol to ethanal (acetaldehyde). It is used as a solvent and in synthetic organic chemistry.
Generalic, Eni. "Cubic close-packed structure." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. 8 Apr. 2025. <https://glossary.periodni.com>.
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