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Explain the relationship between the polarity and boiling points of organic halogen compounds.
Explain the relationship between the polarity and boiling points of organic halogen compounds.
The boiling points of organic halogen compounds are generally higher than the parent hydrocarbons due to their greater polarity and higher molecular mass, which results in stronger intermolecular forces of attraction such as dipole-dipole and van der Waals forces.
Why are the boiling points of chlorides, bromides, and iodides considerably higher than those of hydrocarbons with comparable molecular mass?
Why are the boiling points of chlorides, bromides, and iodides considerably higher than those of hydrocarbons with comparable molecular mass?
The boiling points of chlorides, bromides, and iodides are considerably higher than those of hydrocarbons with comparable molecular mass due to the stronger intermolecular forces of attraction in the halogen derivatives, caused by their greater polarity and higher molecular mass compared to the parent hydrocarbons.
Explain the pattern of variation of boiling points of different alkyl halides.
Explain the pattern of variation of boiling points of different alkyl halides.
For the same alkyl group, the boiling points of alkyl halides decrease in the order: RI > RBr > RCl > RF, due to the increase in size and mass of the halogen atom, leading to stronger intermolecular forces of attraction.
How does the magnitude of van der Waals forces change with the increase in size and mass of the halogen atom in alkyl halides?
How does the magnitude of van der Waals forces change with the increase in size and mass of the halogen atom in alkyl halides?
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What are the main factors that contribute to the differences in boiling points of methyl chloride, methyl bromide, ethyl chloride, and chlorofluoromethanes at room temperature?
What are the main factors that contribute to the differences in boiling points of methyl chloride, methyl bromide, ethyl chloride, and chlorofluoromethanes at room temperature?
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