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Chemistry: Post your doubts here!

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Can someone explain the answers of C(i) and C(ii) ?
I attached the question and mark scheme
paper code: 9701/42/F/M/18Screen Shot 2019-04-20 at 16.29.27.png Screen Shot 2019-04-20 at 16.28.52.png
 
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Hey guys, please help me? The question asks for the reaction of serotonin with Br2 but the mark scheme says that only phenol reacts with it. Doesn't alkene c=c react too? I need an explanation for this. I'm so scared for coming exam :(
Screen Shot 2019-04-21 at 12.37.04 PM.pngScreen Shot 2019-04-21 at 12.37.12 PM.pngScreen Shot 2019-04-21 at 12.37.44 PM.png
 
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upload_2019-4-21_18-43-9.png

upload_2019-4-21_18-43-24.png
may june 2016 42

Can someone explain why in the ms they take the concentration of ch3nh2 as y instead of y - 3.966 x10^-4 ?
 
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Few things to note:
All structural isomers have the same molecular weight of 266.5
Only the chloride ions not bonded to to Cr react (the ones outside the brackets)
n(AgCl) = n(chloride ions)

So, the number of moles of chloride ions outside the brackets is the same as the number of moles of AgCl

For A:
1g of isomer reacts with 3.75x10^-3 mol of AgCl
1g of isomer has 3.75x10^-3 mol of Cl^-1
(1/266.5) mol of isomer has 3.75x10^-3 mol of Cl^-1
3.75x10^-3 mol of isomer has 3.75x10^-3 mol of Cl^-1

This gives us a mole ratio of 1:1 between the isomer and the chloride ions outside the brackets
Therefore, 3-n = 1
n = 2

A is [Cr(H2O)4Cl2]Cl.2H2O

Same reasoning gives n value and molecular formula for B and C.
 
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Having problem/confusion in deducing molecule thorugh NMR pattern.
Taking alot alot of time and it is of only 1-2 or maximum 3 marks.
what should i do not getting better in it?How you people doing?
 
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Having problem/confusion in deducing molecule thorugh NMR pattern.
Taking alot alot of time and it is of only 1-2 or maximum 3 marks.
what should i do not getting better in it?How you people doing?
There are some qs where its of 6 marks the best thing you could for it is Practice, Practice actually helps alot.
 
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For step 4: why is the reagent aqueous Hcl and heat? We are turning amide to amine so shouldn’t it be reduction with LiAlH4?
 

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Also for this one , why is N zero order, why not first? Thanks a lot in advance
 

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For step 4: why is the reagent aqueous Hcl and heat? We are turning amide to amine so shouldn’t it be reduction with LiAlH4?

There is three ways to turn an amide to an amine

1) Acid hydrolysis, using HCL(aq) and heat
This breaks the amide linkage completely and you end up with two molecules, the amine and the acid.
The amine formed will react with the acid to form a salt.

2) Alkaline hydrolysis, using NaOH(aq) and heat
Same as acid, except the amine doesn't form salt, but the acid does.

3) Reduction, using LiAlH4
Here you end up with one molecule, an amine, the carbons in the carboxylic acid group remain attached while the oxygen is removed.
 
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There is two ways to turn an amide to an amine
1) Hydrolysis, using HCL(aq) and heat
This breaks the amide linkage completely and you end up with two molecules, the amine and the acid
2) Reduction, using LiAlH4
Here you end up with one molecule, an amine, the carbons in the carboxylic acid group remain attached while the oxygen is removed
But the amine will react with the acid and form ammonium ion in acidic hydrolysis
 
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