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...f Polycyclic Aromatic Hydrocarbons. Isomer Enumeration of Fused Polycyclic Aromatic Hydrocarbons |journal= Chem. Inf. Comput. Sci. |volume=22 |pages=15–22 |doi ==Bases of the element chart and periodic systems of molecules== ...

...has been developed by Reinhard Schwesinger; the resulting [[phosphazene]] bases are therefore also referred to as Schwesinger [[superbases]].<ref>{{citatio ...a|date=2010|degree=PhD|title=New synthetic methods for biologically active aromatic heterocycles|publisher=Iowa State University|doi=10.31274/etd-180810-2033|d ...

| Odor = Aromatic<ref name=GESTIS/> 1-Octanol [[hydrogen bond|hydrogen bonds]] to [[Lewis bases]]. It is a [[Lewis acid ]] in the [[ECW model]] and its acid parameters are ...

...Os in most cases, the choice of <math>p=4</math> localizes the orbitals in aromatic systems unlike <math>p=2</math>.<ref name=":0" /> ...to the oxygen lone pairs. [[Benzene]] provided an example of a delocalized aromatic system to test the IBO method. Apart from the C-C and C-H σ-bonds, the six ...

There are three major theories relating to the strength of Lewis acids and bases and the interactions between them. #Guttmann [[donor number]]s: for bases the number is derived from the enthalpy of reaction of the base with [[anti ...

...sfn|Lide|2003|loc=Chapter 8: Dissociation Constants of Inorganic Acids and Bases}}{{sfn|Weingärtner et al.|2016|p = 13}}{{efn| | SolubleOther = Poorly soluble in [[haloalkane]]s, [[aliphatic]] and [[aromatic]] hydrocarbons, [[ether]]s.<ref name=chemister>{{cite web| title = Properti ...

...a benzene ring, after the simplest possible such hydrocarbon, [[benzene]]. Aromatic hydrocarbons can be ''monocyclic'' (MAH) or ''polycyclic'' (PAH).}} ...]|content='''[[Base (chemistry)|Base]]'''}}{{defn|defn=In [[chemistry]], ''bases'' are substances that, in [[aqueous solution]], release [[hydroxide]] (OH<s ...