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4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 3-methylcyclohexene. All are colorless volatile liquids classified as a cyclic olefins. They are specialized reagents.
Most methylcyclohexane is extracted from petroleum but it can be also produced by catalytic hydrogenation of toluene: CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. The hydrocarbon is a minor component of automobile fuel, with its share in US gasoline varying between 0.3 and 1.7% in early 1990s [10] and 0.1 to 1% in 2011. [11]
The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/100 ml), unless shown otherwise.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Methylcyclohexanones are a group of three isomers: 2-methylcyclohexanone, 3-methylcyclohexanone, and 4-methylcyclohexanone. [1] They can be viewed as derivative of cyclohexanone. They can be prepared by oxidation of methylcyclohexane as well as partial hydrogenation of the corresponding cresols. All are colorless liquids.
214-752-4; PubChem CID. 14502; UNII: ... Methylcyclohexane; Methylenecyclopropane; References This page was last edited on 20 September 2022, at 17:21 (UTC) ...
Solubility in water. 0.052 g/kg for 1-methylcyclohexene ... Methylcyclohexenes are formed by the partial hydrogenation of toluene to methylcyclohexane over ruthenium ...
-A simple example of the Evelyn effect is the sophomore level chemistry lab experiment involving two popular examples that are listed below. a) Dehydration of 4-methylcyclohexanol [2] Dehydration of 4-methylcyclohexanol.jpeg. b) Dehydration of 2-Methylcyclohexanol [4] Dehydration of 2-Methylcyclohexanol.jpeg