You can use physical properties: melting point, boiling point, odor
Their spectra will be different: IR, UV, NMR
Their reactivity is different: ethene undergo many types of reactions, cyclohexane is fairly unreactive (it is sometimes used as a solvent!
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At room temperature, the halogens like bromine don't react with cyclohexane. Hence the dark brown color of the bromine water remains. When heated, the -H atoms are replaced with -Br(substitution reaction).
Cyclohexane is a six-carbon cyclic compound with the formula C6H12. In its planar representation, it looks like a regular hexagon, but in its 3D representation, it takes on either a chair or boat conformation. It has many uses in organic and analytical chemistry. For more information, see the link below.
Bromine in water or bromine water can be used to distinguish between an alkene and an alkyne. Alkenes will decolorize bromine water by undergoing addition reactions, while alkynes will not react under normal conditions and will not decolorize bromine water.
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Cyclohexane can be converted into benzene by catalytic dehydrogenation in the presence of oxides of D block for ex V2O5, Cr2O3 etc. Cyclohexane when heated at 6000C in presence of Al2O3-Cr2O3 gives benzene.
At room temperature, the halogens like bromine don't react with cyclohexane. Hence the dark brown color of the bromine water remains. When heated, the -H atoms are replaced with -Br(substitution reaction).
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Cyclohexane is a six-carbon cyclic compound with the formula C6H12. In its planar representation, it looks like a regular hexagon, but in its 3D representation, it takes on either a chair or boat conformation. It has many uses in organic and analytical chemistry. For more information, see the link below.
Yes. It has factors in addition to 1 and itself. They are 2 and 17.
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Yes, because all the valencies of carbon atoms are satisfied by sigma bonding and cycloakane does not undergo the addition reactions. However many chemists would say that only alkanes are fully saturated and these have no ring structure and a general formula of CnH2n+2
Bromine in water or bromine water can be used to distinguish between an alkene and an alkyne. Alkenes will decolorize bromine water by undergoing addition reactions, while alkynes will not react under normal conditions and will not decolorize bromine water.
The answer will depend on how the information was entered - in pounds (or ponds) or in pennies, what the operations were - addition/subtraction or -multiplication/division).The answer will depend on how the information was entered - in pounds (or ponds) or in pennies, what the operations were - addition/subtraction or -multiplication/division).The answer will depend on how the information was entered - in pounds (or ponds) or in pennies, what the operations were - addition/subtraction or -multiplication/division).The answer will depend on how the information was entered - in pounds (or ponds) or in pennies, what the operations were - addition/subtraction or -multiplication/division).
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No. Aromaticity depends on a few things. Having all sp2 hybridized bonds being one (which makes the molecule planar or almost flat) - In addition to having sp2 hybridized bonds, you need to have 4n + 2 pi bonded electrons, where n is an integer. This means it needs to have (2, 6, 10, 14.... etc) pi bonded electrons. Cyclohexane does not have the sp2 hybridization requirement needed (all bonds in cyclohexane are sp3 hybridized)
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