Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Same name different structure ?
DubaiAmateurRocketry
National Hazard
****




Posts: 841
Registered: 10-5-2013
Location: LA, CA, USA
Member Is Offline

Mood: In research

[*] posted on 4-1-2014 at 07:05
Same name different structure ?


I took a screen shot of the lecture paper and the same product on sigma alreich.

I am confused which one is the correct one ?


<img src="http://i40.tinypic.com/2mm65o7.jpg" width="800" />

<!-- bfesser_edit_tag -->[<a href="u2u.php?action=send&username=bfesser">bfesser</a>: reduced image size(s)]

[Edited on 4.1.14 by bfesser]
View user's profile View All Posts By User
Nicodem
Super Moderator
*******




Posts: 4230
Registered: 28-12-2004
Member Is Offline

Mood: No Mood

[*] posted on 4-1-2014 at 07:45


What exactly is your question?
It is perfectly normal that equal structures bear an equal name. What else did you expect?
View user's profile View All Posts By User
DubaiAmateurRocketry
National Hazard
****




Posts: 841
Registered: 10-5-2013
Location: LA, CA, USA
Member Is Offline

Mood: In research

[*] posted on 4-1-2014 at 08:05


However the diol groups are placed differently ? I need the compound in the paper for further uses. So how do I know if I shall just buy this or I shall synthesized it my own ? It has same name, same name however different structure.
View user's profile View All Posts By User
Pulverulescent
National Hazard
****




Posts: 793
Registered: 31-1-2008
Member Is Offline

Mood: Torn between two monikers ─ "hissingnoise" and the present incarnation!

[*] posted on 4-1-2014 at 08:14


Quote:
]However the diol groups are placed differently ?.

Two perspectives ─ one molecule . . .




"I know not with what weapons World War III will be fought, but World War IV will be fought with sticks and stones"

A Einstein
View user's profile View All Posts By User
Nicodem
Super Moderator
*******




Posts: 4230
Registered: 28-12-2004
Member Is Offline

Mood: No Mood

[*] posted on 4-1-2014 at 08:26


Quote: Originally posted by DubaiAmateurRocketry  
However the diol groups are placed differently ? I need the compound in the paper for further uses. So how do I know if I shall just buy this or I shall synthesized it my own ? It has same name, same name however different structure.

You are not even funny. There is no difference at all. Both structure are completely identical. If you can't read chemical structures, you should not be messing with chemistry.
View user's profile View All Posts By User
ScienceHideout
Hazard to Others
***




Posts: 391
Registered: 12-3-2011
Location: In the Source
Member Is Offline

Mood: High Spin

[*] posted on 4-1-2014 at 08:35


DAR- I easily see the source of your confusion. We are always spoiled with those 3d-ish stereo molecules with bonds that jump out at you and stuff, and as soon as something is smooshed down into 2d it is rather confusing-

Here is how to clear it up... It always works for me :)

Build a model of this molecule. I don't care if you use a molecular model set or just a computer simulation like Avogadro. Once you build it, focus on the middle carbon. You will soon see that there is nothing different between these 2 molecules, it is just how you are looking at it :D.

Hope that helps,
SciHide




hey, if you are reading this, I can't U2U, but you are always welcome to send me an email!


View user's profile Visit user's homepage View All Posts By User
DubaiAmateurRocketry
National Hazard
****




Posts: 841
Registered: 10-5-2013
Location: LA, CA, USA
Member Is Offline

Mood: In research

[*] posted on 4-1-2014 at 08:37


Quote: Originally posted by Pulverulescent  

Two perspectives ─ one molecule . . .


Ahh right i understood, I thought it was something else. Thank you so much!

Quote: Originally posted by ScienceHideout  
DAR- I easily see the source of your confusion. We are always spoiled with those 3d-ish stereo molecules with bonds that jump out at you and stuff, and as soon as something is smooshed down into 2d it is rather confusing-

Here is how to clear it up... It always works for me :)

Build a model of this molecule. I don't care if you use a molecular model set or just a computer simulation like Avogadro. Once you build it, focus on the middle carbon. You will soon see that there is nothing different between these 2 molecules, it is just how you are looking at it :D.

Hope that helps,
SciHide


Yup I realized, thanks.

and nicodem, sorry for being so stupid, im poor in many parts of chemistry like this one.

[Edited on 4-1-2014 by DubaiAmateurRocketry]
View user's profile View All Posts By User
ScienceHideout
Hazard to Others
***




Posts: 391
Registered: 12-3-2011
Location: In the Source
Member Is Offline

Mood: High Spin

[*] posted on 4-1-2014 at 08:57


Quote: Originally posted by DubaiAmateurRocketry  
Quote: Originally posted by Pulverulescent  

Two perspectives ─ one molecule . . .


Ahh right i understood, I thought it was something else. Thank you so much!

Quote: Originally posted by ScienceHideout  
DAR- I easily see the source of your confusion. We are always spoiled with those 3d-ish stereo molecules with bonds that jump out at you and stuff, and as soon as something is smooshed down into 2d it is rather confusing-

Here is how to clear it up... It always works for me :)

Build a model of this molecule. I don't care if you use a molecular model set or just a computer simulation like Avogadro. Once you build it, focus on the middle carbon. You will soon see that there is nothing different between these 2 molecules, it is just how you are looking at it :D.

Hope that helps,
SciHide


Yup I realized, thanks.

and nicodem, sorry for being so stupid, im poor in many parts of chemistry like this one.

[Edited on 4-1-2014 by DubaiAmateurRocketry]


There is a big difference between being unaware and being stupid... You can't fix stupidity! Being unaware is absolutely forgivable in chemistry, and imagining 3d things on flat pieces of paper is something that comes with much practice and experience. I find it really sad that someone would rather insult you and make you believe that you are stupid than help you understand such a topic.

I am glad that you understand this now... and btw- don't call yourself stupid :). Just by studying chem alone you prove you are not stupid :D!




hey, if you are reading this, I can't U2U, but you are always welcome to send me an email!


View user's profile Visit user's homepage View All Posts By User
bfesser
Resident Wikipedian
*****




Posts: 2114
Registered: 29-1-2008
Member Is Offline

Mood: No Mood

[*] posted on 4-1-2014 at 08:58


Those are both terrible drawings, but they do represent the same molecule. The quaternary carbon (the one with three carbons and a nitrogen bonded to it) is not a <a href="http://en.wikipedia.org/wiki/Stereocenter" target="_blank">stereocenter</a> <img src="../scipics/_wiki.png" />, as two of the attached groups (&ndash;CH<sub>2</sub>OH) are identical. It'd be nice to see the molecule represented with solid and dashed wedges, though, or at the very least with decent bond angles.

[edit] What's worse is that the '3D' models that come up with a <a href="https://www.google.com/search?q=2-ethyl-2-nitro-1,3-propanediol&safe=off&source=lnms&tbm=isch&sa=X&ei=Iz7IUsSKA6SI2wWHlYCgAw &ved=0CAkQ_AUoAQ&biw=1317&bih=655" target="_blank">Google search</a> <img src="../scipics/_ext.png" /> represent it as planar! Not even wrong...

<table><tr><td align="center">2-nitro-2-ethylpropane-1,3-diol.png - 2kB</td></tr><tr><td><em>2-nitro-2-ethylpropane-1,3-diol</em></td></tr></table>
I couldn't get the software to cooperate&mdash;first time using it&mdash;but you get the idea.
Quote: Originally posted by ScienceHideout  
. . . imagining 3d things on flat pieces of paper is something that comes with much practice and experience.
Or autism. ;)

[Edited on 4.1.14 by bfesser]




View user's profile View All Posts By User
ScienceHideout
Hazard to Others
***




Posts: 391
Registered: 12-3-2011
Location: In the Source
Member Is Offline

Mood: High Spin

[*] posted on 4-1-2014 at 09:14


I attached a better picture that I made using marvin... It is a ball and stick model, I would love for someone to post one with wedges, but I can't figure out how to do that... :P



diol.png - 33kB


LOL- I just now noticed that this completely lacks all hydrogens :)

[Edited on 4-1-2014 by ScienceHideout]




hey, if you are reading this, I can't U2U, but you are always welcome to send me an email!


View user's profile Visit user's homepage View All Posts By User
bfesser
Resident Wikipedian
Thread Moved
4-1-2014 at 09:32

  Go To Top