141.1 C from ptcl.chem.ox.ac.uk/MSDS/PR/propanoic_acid.html
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.
Out of methane, ethane, propane, and butane, butane has the highest boiling point.
Butane would have the highest boiling point among ethane, propane, and butane.
The boiling point of ethyl alcohol is higher than that of dimethyl ether because ethyl alcohol has stronger intermolecular forces (hydrogen bonding) between its molecules than dimethyl ether, which only has weaker van der Waals forces. These stronger intermolecular forces in ethyl alcohol require more energy to overcome, resulting in a higher boiling point.
C3H8 (propane) has a higher boiling point than C2H6 (ethane) because propane has a larger molecular size and stronger van der Waals forces between its molecules, which require more energy to break and transition to the gas phase.
Dimethyl ether (DME) has a boiling point of -24.8°C, and propane has a boiling point of -42.1°C. Therefore, dimethyl ether propane would have a boiling point that falls between these two values, likely around -30°C to -35°C.
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.
Out of methane, ethane, propane, and butane, butane has the highest boiling point.
Butane would have the highest boiling point among ethane, propane, and butane.
The boiling point of ethyl alcohol is higher than that of dimethyl ether because ethyl alcohol has stronger intermolecular forces (hydrogen bonding) between its molecules than dimethyl ether, which only has weaker van der Waals forces. These stronger intermolecular forces in ethyl alcohol require more energy to overcome, resulting in a higher boiling point.
The OH group in ethanol is highly hydrogen bonded which requires much more heat energy to break before boiling can occur. Dimethyl ether, which has the same molecular formula and molecular weight does not have this due to the ether linkage.
The boiling point of propane is in the range -42,25 oC to -42,04 oC.
C3H8 (propane) has a higher boiling point than C2H6 (ethane) because propane has a larger molecular size and stronger van der Waals forces between its molecules, which require more energy to break and transition to the gas phase.
I think propane is higher??
Propane has a low boiling point, around -44 degrees Celsius, which means it evaporates easily at room temperature. Additionally, propane molecules are relatively small and have weak intermolecular forces, allowing them to escape as a gas readily.
At ordinary atmospheric pressures propane is in the gas phase at 0C.
Think in terms of room temperature. Hexane is a liquid that is flammable, but is used in cleaning solvents and stuff like around the garage. Propane is the gas that comes in a steel bottle that you use for gas stoves and barbeque grills. So if you let propane out into the room its a gas and so it already past its boiling point. So the boiling point of Hexane is hotter than room temperature and the boiling point of propane is lower than room temperature. The actual numbers are 69 C and -42 C.