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Organic Chemistry

Hot goIITian

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23 Nov 2008 02:58:55 IST
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screwed up..end sem paper doubt..IIT kgp...help..
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hey janta...pls help me...tomoro is my end sem exam n i have no clue abt butane gauche interactions in 1,2 dimethycyclohexane...pls help me...iit end sems are also like jee...i dunno wat will happen..pls help me...mail me on gaurav3sharma@gmail.com pls janta hel help...


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kishore subramanian's Avatar

Blazing goIITian

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23 Nov 2008 04:16:41 IST
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Axial bonds are perpendicular to the plane of the ring


Equatiorial bond are in the plane of the ring. 


Hot goIITian

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23 Nov 2008 04:18:43 IST
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i know this crap..i wana know abt butane gauche interaction dude!!

kishore subramanian's Avatar

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23 Nov 2008 04:25:25 IST
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In boat formation crowding takes place.The most crowding is when the Three axial bonds have atoms on same side of the molecule. Due to the this boat form changes to chair form.


In di substituted  cyclohexanes will assume chair conformation containing both substituents in equatorial orentiation.


Hot goIITian

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23 Nov 2008 04:26:57 IST
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i think u dint get my question !!

kishore subramanian's Avatar

Blazing goIITian

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23 Nov 2008 04:27:17 IST
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Do u want those circular newman projections??//

kishore subramanian's Avatar

Blazing goIITian

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23 Nov 2008 04:28:14 IST
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No i didnt get u'r ques....


Hot goIITian

Joined: 7 Aug 2007
Posts: 184
23 Nov 2008 04:28:30 IST
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dude i want everything abt butane gauche interactions...n u r telling me stereochemistry of cyclohexane !!

kishore subramanian's Avatar

Blazing goIITian

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23 Nov 2008 04:34:25 IST
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In newman's projection angle between teo methyl groups are seperated by 600 angle is called guach conformer.


There is more steric strain on gauche conformer as methyl groups are together. Steric strain in guache conformer is called guache interaction.


Hot goIITian

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23 Nov 2008 04:35:57 IST
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can u tell me how many gauche interactions are there in the compund i mentioned??

kishore subramanian's Avatar

Blazing goIITian

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23 Nov 2008 04:37:39 IST
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Sorry i dont remember.....




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