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Author: Subject: Help with Boiling Points
Muzz1969
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[*] posted on 23-7-2015 at 04:58
Help with Boiling Points


Hi everyone,


I'm looking for some help with intermolecular forces and there relation to boiling points. I have 3-methylbutanal and 2-methylpropanol. One has a carboxylic and the other has and aldehyde function group.

My question is, is it the different function groups and only the different groups that change the boiling point of these two very similar molecules or are there other factors involved.
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smaerd
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[*] posted on 23-7-2015 at 05:16


Functional groups are a way of describing the structure of a molecule. In this case there are two factors to consider.

First lets look at the functional groups, we have an alcohol and an aldehyde(not a carboxylic acid, be careful!). The aldehyde can accept hydrogen bonds at the carbonyl oxygen. It doesn't have a viable hydrogen bond donor however. Whereas the alcohol can accept and donate to form hydrogen bonds. So from this perspective, we can say that the alcohol compound, 2-methylpropanol, should have the strongest attraction to other molecules of the same variety compared to the aldehyde. I hope that makes sense. The other functional groups present on either molecule is the alkane functional group.

The alkane part of both molecules at first glance looks the same. Look closely though, the propanol is one carbon shorter in length than the butanal compound. This means they aren't isomers and one has a greater molecular weight. Molecular weight also effects boiling point (takes more energy to lift/boil something that is heavy). High molecular weight compounds also have more interactions. Consider a weak intermolecular force such as van der waals(london dispersion) and look at methanes boiling point, verses octane. Large difference there.

So the intermolecular forces dictate a lot of boiling point phenomena, but so does the molecular weight, and orientation of bonds (different isomers even stereoisomers can have stronger/weaker IM forces). In this case the orientation of the alkane chain bonds are essentially the same, so that can sort of be ruled out for general considerations.

I hope this helps. Analyzing structure and gaining an intuition about chemicals is a skill that is very important!

[Edited on 23-7-2015 by smaerd]




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Muzz1969
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[*] posted on 23-7-2015 at 05:33


Thanks for that , I'll begin to digest what you have said and shoot back some more questions. This is my first organic unit at uni.
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Muzz1969
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[*] posted on 23-7-2015 at 05:41


Ok one question doesn't the O=C-OH on the 2-Methylpropanoic Acid make it a Carboxylic function Group and alcohol function group does not have the double bond

[Edited on 23-7-2015 by Muzz1969]
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[*] posted on 23-7-2015 at 05:44


Quote: Originally posted by Muzz1969  
Ok one question doesn't the O=C-OH on the 2-Methylpropanoic Acid make it a Carboxylic function Group
Well, in your first post you said 2-methylpropanol, but if that's actually what you meant, then yes, it would be a carboxylic acid.



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Muzz1969
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[*] posted on 23-7-2015 at 05:48


Quote: Originally posted by zts16  
Quote: Originally posted by Muzz1969  
Ok one question doesn't the O=C-OH on the 2-Methylpropanoic Acid make it a Carboxylic function Group
Well, in your first post you said 2-methylpropanol, but if that's actually what you meant, then yes, it would be a carboxylic acid.



Sorry yes i made a typo on that my bad.
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Muzz1969
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[*] posted on 23-7-2015 at 06:24


Sorry about my mistake, how does that now change things from the point of my original questiion.
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