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Heptane or n-heptane is the straight-chain alkane with the chemical formula H 3 C(CH 2) 5 CH 3 or C 7 H 16. When used as a test fuel component in anti-knock test engines, a 100% heptane fuel is the zero point of the octane rating scale (the 100 point is 100% iso-octane ).
Carl Schaschke, 2014, A Dictionary of Chemical Engineering, Oxford University Press. G. I. Nikishin, Yu. N. Ogibin & L. Kh. Rakhmatullina, 1975, ‘Peroxydisulfate-initiated reactions of 1-heptene with acetic and propionic acids’, Bulletin of the Academy of Sciences of the USSR, Division of chemical science, volume 23, pages1479–1483
It is an heptane molecule with a methyl group attached to its second atom. It is a flammable colorless liquid used as fuel. [2] If the standard definition of the prefix "iso-" is strictly used then 2-methylheptane can be called "Isooctane". However this name is usually used for another much more important isomer of octane 2,2,4-trimethylpentane ...
It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol .
Norbornane (also known as bicyclo[2.2.1]heptane) is an organic compound and a saturated hydrocarbon with chemical formula C 7 H 12. It is a crystalline compound with a melting point of 88 °C . The carbon skeleton is derived from cyclohexane ring with a methylene bridge in the 1,4- position, and is a bridged bicyclic compound.
2,2,4-Trimethylpentane, also known as isooctane or iso-octane, is an organic compound with the formula (CH 3) 3 CCH 2 CH(CH 3) 2.It is one of several isomers of octane (C 8 H 18).This particular isomer is the standard 100 point on the octane rating scale (the zero point is n-heptane).
Norcarane, or bicyclo[4.1.0]heptane, is a colorless liquid. It is an organic compound prepared using the Simmons–Smith reaction , by the action of diiodomethane and a zinc-copper couple on cyclohexene in diethyl ether .
The two heptane radical rings then untwist to an unstrained conformation, and finally the dimer fragments back into two cis-cycloheptene molecules. Note that the photoisomerization of maleic acid to fumaric acid with bromine is also bimolecular.