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2,3-Dimethylhexane Skeletal formula of 2,3-Dimethylhexane: Ball and stick model of 2,3-dimethylhexane: Names Preferred IUPAC name. 2,3-Dimethylhexane [1] Identifiers
2,5-Dimethylhexane; 3,3-Dimethylhexane; 3,4-Dimethylhexane [Wikidata This page was last edited on 27 April 2022, at 16:52 (UTC). Text is available under the ...
In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12. The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the " -ene " suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond .
3-Hexyne is the organic compound with the formula C 2 H 5 CCC 2 H 5. This colorless liquid is one of three isomeric hexynes. 3-Hexyne forms with 5-decyne, 4-octyne, and 2-butyne a series of symmetric alkynes. It is a reagent in organometallic chemistry. [1] Structure of the coordination complex NbCl 3 (dimethoxyethane)(3-hexyne). [2]
Cyclohexene is a hydrocarbon with the formula (CH 2) 4 C 2 H 2. It is a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon. [3]
3-Methylcyclohexene; 4-Methylcyclohexene This page was last edited on 18 November 2024, at 14:45 (UTC). Text is available under the Creative Commons Attribution ...
C 2 H 4 + 1/ 2 O 2 → C 2 H 4 O. Alkenes react with ozone, leading to the scission of the double bond. The process is called ozonolysis. Often the reaction procedure includes a mild reductant, such as dimethylsulfide (SMe 2): RCH=CHR' + O 3 + SMe 2 → RCHO + R'CHO + O=SMe 2 R 2 C=CHR' + O 3 → R 2 CHO + R'CHO + O=SMe 2
(CH 3) 3 C-CH=C(CH 3) 2 + CH 2 =CH 2 → (CH 3) 3 C-CH= CH 2 + (CH 3) 2 C= CH 2. It is a building block to synthetic musks by its reaction with p-cymene. It is also used in the industrial preparation of terbinafine. [1] In the study of C-H activation, neohexene is often used as a hydrogen acceptor. [2]