Boiling point of ethers and alkanes

AI Thread Summary
Ethers typically have higher boiling points than alkanes due to dipole-dipole interactions, but this trend can be inconsistent with larger alkanes. For example, hexane has a higher boiling point than ethyl-propyl ether, and diethyl ether has a higher boiling point than pentane, while butane surpasses ethyl methyl ether. The boiling point of alkanes increases with chain length due to enhanced Van der Waals interactions, which explains why longer, unbranched alkanes can have higher boiling points than certain ethers. The discussion highlights that the principle regarding boiling points is a general rule of thumb and may not hold true in all cases.
Queequeg
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My organic chemistry textbook says that ethers generally have higher boiling points than alkanes because of dipole-diole interactions, but why then does hexane have a higher boiling point than ethyl-propyl-ether? Is this principle then not true for larger alkanes with 5 or more carbons? Diethyl ether also has a higher boiling point than pentane, but then butane has a higher B.P than ethyl methyl ether.
 
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2 reasons:

1) As an alkane or alkyl gets longer but does not branch, its BP increases b/c it can have more Van der Waals interactions; thus, ethyl-propyl-ether has a higher bp than ethyl methyl ether;;; hexane has a higher BP than pentance, etc. hope this helps.
 
Queequeg said:
My organic chemistry textbook says that ethers generally have higher boiling points than alkanes because of dipole-diole interactions

IMHO "generally" suggests it is just a rule of thumb, and as such can often fail.
 
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