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2. File:Organic Chemistry.pdf - Wikipedia

   en.wikipedia.org/wiki/File:Organic_Chemistry.pdf

   You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

3. John E. McMurry - Wikipedia

   en.wikipedia.org/wiki/John_E._McMurry

   McMurry's most popular textbook Organic Chemistry was first printed in 1984. In 2022, he sold the rights for the book to OpenStax making it free for the user. [3] [4] Among his other texts are: Organic Chemistry with Biological Applications (3rd edition) [5] Chemistry (8th edition) [6] General Chemistry, Atoms First (2nd edition) [7]

4. Icosane - Wikipedia

   en.wikipedia.org/wiki/Icosane

   Icosane (alternative spelling eicosane and eichosane [2]) is an alkane with the chemical formula C 20 H 42.It has 366,319 constitutional isomers.. n-Icosane (the straight-chain structural isomer of icosane) is the shortest compound found in paraffin waxes used to form candles.

5. Portal:Chemistry/Textbook - Wikipedia

   en.wikipedia.org/wiki/Portal:Chemistry/Textbook

   absorption - adsorbent - adsorption - aeration - aerosol - alkali metal - alkaline earth - alkaline earth metal - allotrope - alloy - amalgam - analysis - atom - boiling - boiling point - chemical change - chemical element - chemical property - chromatography - colloid - column chromatography - compound - concentration - condensation - congener - crystallization - density - dialysis (chemistry ...

6. IUPAC Color Books - Wikipedia

   en.wikipedia.org/wiki/IUPAC_Color_Books

   Quantities, Units and Symbols in Physical Chemistry, commonly known as the Green Book, is a compilation of terms and symbols widely used in the field of physical chemistry. It also includes a table of physical constants, tables listing the properties of elementary particles, chemical elements, and nuclides, and information about conversion ...

7. Allylic strain - Wikipedia

   en.wikipedia.org/wiki/Allylic_strain

   Allylic strain in an olefin. Allylic strain (also known as A 1,3 strain, 1,3-allylic strain, or A-strain) in organic chemistry is a type of strain energy resulting from the interaction between a substituent on one end of an olefin (a synonym for an alkene) with an allylic substituent on the other end. [1]

8. Cyclododecahexaene - Wikipedia

   en.wikipedia.org/wiki/Cyclododecahexaene

   12) is a member of the series of annulenes with some interest in organic chemistry with regard to the study of aromaticity. [1] Cyclododecahexaene is non-aromatic due to the lack of planarity of the structure. [citation needed] On the other hand the dianion with 14 electrons is a Hückel aromat and more stable.

9. Three-center four-electron bond - Wikipedia

   en.wikipedia.org/wiki/Three-center_four-electron...

   The 3-center 4-electron (3c–4e) bond is a model used to explain bonding in certain hypervalent molecules such as tetratomic and hexatomic interhalogen compounds, sulfur tetrafluoride, the xenon fluorides, and the bifluoride ion.