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Topic: Melting Point of Isomers...  (Read 1721 times)

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Offline khamil10

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Melting Point of Isomers...
« on: November 30, 2014, 05:43:52 PM »
Why does 1-bromo-4-nitrobenzene have a higher melting point than 1-bromo-2-nitrobutane?

Offline Arkcon

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Re: Melting Point of Isomers...
« Reply #1 on: November 30, 2014, 07:57:37 PM »
What does melting mean?  What is used to cause melting, and what effect does it have on a compound?   For that matter, what is the difference between the two molecules in this question?

I ask the questions to help you help your self.  Its more intersecting interesting for us, and less like cheating for you.  That's all in the Forum Rules{click}.

*[EDIT]*  Silly autocorrect
« Last Edit: December 01, 2014, 07:57:30 AM by Arkcon »
Hey, I'm not judging.  I just like to shoot straight.  I'm a man of science.

Offline khamil10

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Re: Melting Point of Isomers...
« Reply #2 on: November 30, 2014, 09:14:42 PM »
I'm sorry, very new to this. It actually just took me forever to know how to reply.

My thought was that the symmetry of 1-bromo-4-nitrobenzene meant that is was more easily locked into the crystal lattice structure which meant that more energy (heat) was needed to break the crystal lattice structure leading to a higher melting point than 1-bromo-2-nitrobenzene.

I should have included my ideas so that it didn't seem like I was fishing for someone to do my work. Sorry.

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