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What happens when ethanol is heated with concentrated sulphuric acid at 170 C?

There is formation of ethoxy ethane. (ether)


Is petroleum ether miscible with ethanol?

Yes, petroleum ether is generally not miscible with ethanol. They are immiscible due to differences in their polarities and intermolecular forces. Petroleum ether is a nonpolar solvent, while ethanol is a polar solvent, making them unable to mix well.


Which has a lower enthalpy ethanol or dimethyl ether?

Dimethyl ether has a lower enthalpy compared to ethanol because dimethyl ether has a simpler structure and weaker intermolecular forces, leading to lower enthalpy values. Ethanol has more complex molecular structure and stronger intermolecular forces, resulting in higher enthalpy values.


Why ethanol has a higher boiling point than dimethyl ether?

Ethanol has a higher boiling point than dimethyl ether because ethanol molecules have stronger intermolecular forces due to hydrogen bonding, while dimethyl ether only has weaker dipole-dipole forces. These stronger hydrogen bonds in ethanol require more energy to break, resulting in a higher boiling point compared to dimethyl ether.


Why boiling point of ethnol is higher then ether?

The higher boiling point of ethanol compared to ether is due to stronger intermolecular forces in ethanol. Ethanol molecules have hydrogen bonding and dipole-dipole interactions, which require more energy to overcome, leading to a higher boiling point. Ether has weaker van der Waals forces between molecules, resulting in a lower boiling point.


Is it possible to have an isomer of ethane?

Yes, it is possible to have an isomer of ethane. Isomers are molecules with the same molecular formula but different structural arrangements. Ethane has one isomer called dimethyl ether, which has a different arrangement of atoms.


Why ethanol has higher boiling point than diethyl ether?

Ethanol has a higher boiling point than diethyl ether because it can form hydrogen bonds due to the presence of the hydroxyl group. These hydrogen bonds increase the intermolecular forces between ethanol molecules, requiring more energy to break them apart and reach the boiling point compared to diethyl ether, which lacks this ability to form hydrogen bonds.


Why ethanol has high boiling point than diethyl-ether?

Ethanol has a higher boiling point than diethyl ether because ethanol has stronger intermolecular forces due to hydrogen bonding. Hydrogen bonding creates attractions between ethanol molecules, requiring more energy to separate them compared to the weaker London dispersion forces present in diethyl ether. This results in a higher boiling point for ethanol.


What areTwo compound same molecular formula C2H6O?

This can be either: ethanol : C2H5OH which is an alcohol or dimethyl ether (methoxymethane) CH3OCH3 which is an ether. These are examples of functional group isomers. Regards, Denison - gofortraining@gmail.com


Why ethanol has a higher boiling point than diethyl ether?

Ethanol has a higher boiling point than diethyl ether because ethanol can form hydrogen bonds due to the presence of the hydroxyl group, leading to stronger intermolecular forces. Diethyl ether, on the other hand, cannot form hydrogen bonds and relies on weaker dipole-dipole interactions, resulting in a lower boiling point.


What formula is c2h40?

The formula C2H4O can represent both ethanol and dimethyl ether. Ethanol is a common alcohol used in beverages and as a fuel, while dimethyl ether is a volatile compound used as a propellant and refrigerant.


Is dimethyl ether a structural isomer?

Yes it is. It's structural isomer is ethanol C2H5OH