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covalent bond
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Why is there an extraordinary difference in melting points between cyclohexane and cyclohexene?
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.
Is cyclohexene soluble in ligroin?
Cyclohexene is very miscible with other organic solvents.
Why does benzene produce a sootier flame than either cyclohexane or cyclohexene?
It is because the cyclohexene is an unsaturated compound. It contain one or more carbon-carbon double bond in a ring structure and this bonding still can be reduced by adding hydrogen atoms (combustion process). Thus,it will more reactive compare to cyclohexane, a saturated compound that all the carbon atoms within it have been bond with hydrogen atoms. As the result, the cyclohexene will produces a sootier flame than cyclohexane.
What result occurs adding ethyl cyclohexene to Bromine?
Cyclohexene picks up the bromine from solution and becomes dibromoethylcyclohexane.
Why is the density of water less in Cyclohexene?
Yes, water is denser than cyclohexene due to hydrogen bonding.
What is the structure of cyclohexene Is the compound saturated or unsaturated Explain?
Cyclohexene is an unsaturated molecule because contain a double bond and has a ring structure.
Why is there an extraordinary difference in melting points between cyclohexane and cyclohexene?
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.
The major alkene product produced by dehydrating Cyclohexanol?
cyclohexene - a 6 carbon ring with one double bond
Is cyclohexene a polar or non polar?
Nonpolar. There's a slight amount of polarity because of the double bond, but not much.
Why the brown color of bromine disappear when mixed with cyclohexene?
Halogens react with alkenes to form haloalkanes. Addition of the bromine in this case occurs across the double bond in cyclohexene. The resultant products are colourless hence the brown colour disappears.
What type of reaction is Cyclohexene and Bromine?
Electrophilic addition. Forms 1,2,-dibromocyclohexane
What is reaction of cyclohexene with H2O and H plus catalyst?
Cyclopentene has a double bond in it. So when it reacts with H20, the double bond will break. In its place, the cyclopentene molecule will gain a OH and an H.
Is cyclohexene soluble in ligroin?
Cyclohexene is very miscible with other organic solvents.
Is cyclohexene soluble in water?
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.
Why does benzene produce a sootier flame than either cyclohexane or cyclohexene?
It is because the cyclohexene is an unsaturated compound. It contain one or more carbon-carbon double bond in a ring structure and this bonding still can be reduced by adding hydrogen atoms (combustion process). Thus,it will more reactive compare to cyclohexane, a saturated compound that all the carbon atoms within it have been bond with hydrogen atoms. As the result, the cyclohexene will produces a sootier flame than cyclohexane.
What result occurs adding ethyl cyclohexene to Bromine?
Cyclohexene picks up the bromine from solution and becomes dibromoethylcyclohexane.
In which type of bond are electrons?
Electrons are shared in a type of bond known as covalent. This type of bond is also considered a chemical bond.
