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3 Feb 2007 12:39:58 IST
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What happens when glucose is treated with large amount of PCl5?
Will all the -OH groups get substituted by -Cl?
Also what happens when glucose is oxidised with strong oxidizing agents?


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Blazing goIITian

Joined: 24 Dec 2006
Posts: 1312
3 Feb 2007 14:27:07 IST
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i dunno exactly but i know for sure that an atom cannot have more than one OH radical becuz then it becomes unstable....u have to remove a water molecule from it and then u r left with either a ketone or a aldehyde....i may be wrong but on the whole......the fact remains true

Blazing goIITian

Joined: 24 Dec 2006
Posts: 1312
3 Feb 2007 14:29:51 IST
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for eg .
H
|
H--C--OH
|
OH
is unstable
we remove a water molecule and get

H - CHO
FormAldehyde

this may be applicalbe to ur first query

Blazing goIITian

Joined: 24 Dec 2006
Posts: 1312
3 Feb 2007 14:33:09 IST
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for eg .
H
|
H--C--OH
|
OH
is unstable
we remove a water molecule and get

H - CHO
FormAldehyde

this may be applicalbe to ur first query

* consider the four bonds on C....its difficult to draw with all the dashes
CyBorG's Avatar

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Joined: 6 Jan 2007
Posts: 706
6 Feb 2007 17:52:37 IST
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Hey KIRAN try this!!!
Kiran H's Avatar

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Joined: 7 Nov 2006
Posts: 296
9 Feb 2007 20:32:52 IST
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Hi Adarsh
 
Sorry for the delay.
 
PCl5 is a good dehydrating agent. So it replaces all the OH groups in glucose. The aldehydic group is untouched.
 
Reason for this is observed by drawing the Ring structure, The pyranose ring.
And hence the OH groups are  replacable.
 
Njoy! 



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