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12 relations: Cycloaddition, Cyclohexene, Dehydrohalogenation, Diels–Alder reaction, Electrocyclic reaction, Isomer, Organic compound, Photochemistry, Pine oil, Terpinene, Transition metal alkene complex, 1,4-Cyclohexadiene.
Cycloaddition
A cycloaddition is a pericyclic chemical reaction, in which "two or more unsaturated molecules (or parts of the same molecule) combine with the formation of a cyclic adduct in which there is a net reduction of the bond multiplicity." The resulting reaction is a cyclization reaction.
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Cyclohexene
Cyclohexene is a hydrocarbon with the formula C6H10.
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Dehydrohalogenation
Dehydrohalogenation is a chemical reaction that involves removal of (elimination of) a hydrogen halide from a substrate.
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Diels–Alder reaction
The Diels–Alder reaction is an organic chemical reaction (specifically, a cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative.
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Electrocyclic reaction
In organic chemistry, an electrocyclic reaction is a type of pericyclic rearrangement where the net result is one pi bond being converted into one sigma bond or vice versa.
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Isomer
An isomer (from Greek ἰσομερής, isomerès; isos.
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Organic compound
In chemistry, an organic compound is generally any chemical compound that contains carbon.
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Photochemistry
Photochemistry is the branch of chemistry concerned with the chemical effects of light.
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Pine oil
Pine oil is an essential oil obtained by the steam distillation of stumps, needles, twigs and cones from a variety of species of pine, particularly Pinus sylvestris.
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Terpinene
The terpinenes are a group of isomeric hydrocarbons that are classified as monoterpenes.
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Transition metal alkene complex
In organometallic chemistry, a transition metal alkene complex is a coordination compound containing one or more alkene ligands.
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1,4-Cyclohexadiene
1,4-Cyclohexadiene is an organic compound with the formula C6H8.
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1,2-dihydrobenzene, 1,3-CHD, 1,3-cyclohexadiene, 1-3-cyclohexadiene, Cyclohexane-1,3 diene.
