A New Unifying Biparametric Nomenclature that Spans all of by Seymour B. Elk

By Seymour B. Elk

Content material:
Preface

, Pages v-x
Chapter 1 - Introduction

, Pages 1-48
Chapter 2 - Non-integer bonds

, Pages 49-114
Chapter three - different major transformations from current systems

, Pages 115-166
Chapter four - Oxidation numbers

, Pages 167-179
Chapter five - The boranes and similar aluminum compounds

, Pages 180-205
Chapter 6 - Spiro and comparable compounds

, Pages 206-257
Chapter 7 - Topologically restricted compounds

, Pages 258-268
Chapter eight - Polymers

, Pages 269-292
Chapter nine - Molecular Rearrangement

, Pages 293-303
Index

, Pages I1-I7

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Additional resources for A New Unifying Biparametric Nomenclature that Spans all of Chemistry. The science of incorporating daily over 2,000 new names to a base of over 42 million compounds while still maintaining order

Example text

To the contrary, because atomic symbols are included in the first "layer of information" about a chemical moiety, there is no need to create a second layer of information in which the names of the different atoms are listed. This inclusion of atom symbols immediately makes for a more user-friendly nomenclature, especially for rapidly scanning a name to see whether it is the moiety under consideration. The extension of this coding system to monocycles is straightforward: Instead of an atom at the end of a path being labeled as locant #1, there is no end to a ring; consequently, the highest atomic number atom in a ring is designated as locant #1.

This edge may be at either the top or the bottom of the figure. Moreover, for polygons with 4n edges, exactly two of the edges should be horizontal. All remaining edges beside those set vertically or horizontally should be as evenly distributed as possible. Observe that, in order to maintain its association with benzene, the center ring of Figure 8 does not subscribe to this implied convention. Additionally, this note acknowledges that, from lUPAC's perspective, selected deformations in the plane are desirable.

E.. 31 HICIH (1) Before describing how the remaining two hydrogen atoms are attached to this longest chain, observe that selected entire molecules (those that are strictly linear in the graph theoretical sense) can be nomenclated in an identical manner. For example, the carbon dioxide and water molecules are simply: 02C20 (2) HIOIH (3) and respectively . In order to now incorporate the two remaining hydrogen atoms into the canonical name for methane, the algorithm is: at the end of the code of the principal chain place a colon followed by the locant number of the atom to which each secondary chain is to be attached.

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