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Cyclohexene is an unsaturated molecule because contain a double bond and has a ring structure.
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Cyclohexene + 4 H2O2 --> (in presence of NaWO3 * 2H2O and Phase Transfer Catalyst) yeilds adipic acid and 4H2O
if cyclohexene is prepared by dehydration of cyclohexanol in the presence of a strong acide like H3PO4, sodium carbonate will be used to neutralize the acidic medium
Cyclohexene is a volatile liquid Thus, the flask is cooled to reduce the degree of evaporation to a minimum
Cyclohexene is very miscible with other organic solvents.
No, cyclohexene is not soluble in water. Cyclohexene is a nonpolar compound, while water is a polar solvent. Generally, nonpolar compounds are not soluble in polar solvents like water. Therefore, cyclohexene tends to be immiscible or insoluble in water.
The extraordinary difference in melting points between cyclohexane and cyclohexene is due to the difference in shape. Cyclohexene has an awkward geometry to stack with sp2 hybridized bond angles. This lends to an extreme low melting point for cyclohexene.
Cyclohexene picks up the bromine from solution and becomes dibromoethylcyclohexane.
colourless
Cyclohexene is an unsaturated molecule because contain a double bond and has a ring structure.
Yes, water is denser than cyclohexene due to hydrogen bonding.
Yes, cyclohexene has lower boiling point than cyclohexanol (and cyclohexane as well)
The answer is 0,1021 moles.
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.8111 g/ml
covalent bond