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Chemistry: Post your doubts here!

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Notice that before hydrolysis, we have total 5 alcohols, one primary alcohol, the one projecting upwards on top left, and the other 4 are all primary, because all of them are bonded to a carbon which, in turn, is bonded to another carbon.
After hydrolysis, the Cls will be replaced by OH, our primary alcohol remains the same as 1, secondary increase by 1, because another secondary has been added when the left sided chlorine gets replaced by OH. The Cl on the very right, gets replaced by OH as well, but since it is bonded to a carbon atom, which in turn, is bonded to more than 2 carbon atoms, that one becomes a tertiary alcohol. That leaves us with the option C.
I got it thanks. I had been confusing sth.
 
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can someone please explain this qs? :/
 

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When M is reacted under acidic conditions with HCl, the two reactions that occur are the hydrolysis of ester, and amide present in this compound (it has been indicated in the diagram above).

The hydrolysis of these will give you two compounds:
HO2CCH2OH and HO2CCH2NH2

As the conditions are acidic, the amine produced would be protonated under acidic conditions, giving HO2CCH2NH3+, hence the answer will be B.
 
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How comes the answer is C? Silver nitrate and ammonia solution are used to test halides, not alcohols!! :(
a li'l explanation please!


q20.jpg
 
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View attachment 60354
When M is reacted under acidic conditions with HCl, the two reactions that occur are the hydrolysis of ester, and amide present in this compound (it has been indicated in the diagram above).

The hydrolysis of these will give you two compounds:
HO2CCH2OH and HO2CCH2NH2

As the conditions are acidic, the amine produced would be protonated under acidic conditions, giving HO2CCH2NH3+, hence the answer will be B.
I get that. I find it a bit difficult to visualize the products tho.
 
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W1041 part c 2. Why does the alkene not split when the reagent used is hot KMno4?
6 c ii?
It does split mate. One in the C=C, one is holding to an H, which produces COOH when ooxidised, the other is bonded to two Carbons, so it makes a ketone
 
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can someone please explain this qs? :/
Well to be honest there isn't much explanation for this.
You just had to know that white phosphorus (the very reactive allotrope of phosphorus) is P4... A tetrahedral structure. As the mark scheme shows, you can connect them all such that each P atom has three bonds.
Over time, white phosphorus tends to change into red phosphorus. In fact, by heating up white phosphorus above 250 degrees, this process can be accelerated to form red phosphorus from white phosphorus. One of the P-P bonds in white phosphorus molecule breaks to form a bond with a neighboring P4 molecule. This is just like polymerisation. So you can show any length of this chain in your diagram.

So to summarize, white phosphorus is P4 and red phosphorus is just a bunch of P4's joined together.

As for whether this is in our syllabus, I have no idea.
 
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Well to be honest there isn't much explanation for this.
You just had to know that white phosphorus (the very reactive allotrope of phosphorus) is P4... A tetrahedral structure. As the mark scheme shows, you can connect them all such that each P atom has three bonds.
Over time, white phosphorus tends to change into red phosphorus. In fact, by heating up white phosphorus above 250 degrees, this process can be accelerated to form red phosphorus from white phosphorus. One of the P-P bonds in white phosphorus molecule breaks to form a bond with a neighboring P4 molecule. This is just like polymerisation. So you can show any length of this chain in your diagram.

So to summarize, white phosphorus is P4 and red phosphorus is just a bunch of P4's joined together.

As for whether this is in our syllabus, I have no idea.
even i was wondering if its there :/
but thank you i understood the explanation
 
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Can someone please explain these polymer questions
M/j/13/41 q8 the first part
and m/j/13/42 q8 8 b(i)
URGENT !!
 

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