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Reply 20
what mechanisms are we meant to know?
Reply 21
Nucleophilic addition(-elimination) and substitution, and electrophilic add/sub.

Free radical from AS.

Also napthalene-2-ol came up in Jan! So sneaky but it was in the revision guide... It forms a RED azo dye. Phenol is yellow.
Reply 22
How did everyone find it? I thought it was considerably harder than past papers.


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Reply 23
Original post by x_leah27_x
How did everyone find it? I thought it was considerably harder than past papers.


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That one about the isomer (molecules L and M) blew me; I had to rush the rest of the paper but just finished in time after furiously scribbling a 4-chlorobenzoic acid molecule and 35Cl and 37Cl. Hope it gets the marks!
Reply 24
Thought overall it was okay! :smile: Only things that threw me were 5)b) where we had to find L and M and then the maths part of question 3, but otherwise it was alright


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Reply 25
Anybody else get 1 for the number of moles present of water in that molecule?
Reply 26
Yeah I had 1 too


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Reply 27
Original post by Picksel8
Anybody else get 1 for the number of moles present of water in that molecule?


I did!! :biggrin: Sorry I'm slightly relieved someone else had the same answer to me, I spent about 15 minutes staring at that question trying to figure out how to answer it :P
Reply 28
I left it when I first saw it and thought there was no way I was going to answer i, got there in the end though!


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Reply 29
Original post by rach-ell
I did!! :biggrin: Sorry I'm slightly relieved someone else had the same answer to me, I spent about 15 minutes staring at that question trying to figure out how to answer it :P


Good good, it looked harder than it was to be fair, was just a case of getting the relevant information out of that ridiculously large paragraph!

The molecule M, what did people get? I had something like

CH3-CH2-CO-NH-C6H5-NH2

I think I may have remembered what i put down wrong though, it was something like that
Reply 30
I didnt get 1 because my Mr came out as 0.84 for some reason which was obviously wrong! but couldn't figure out where I'd gone wrong :frown: My friend got 1 though :smile:
Reply 31
The opening question was probably the hardest opening question on a CH4 paper I've done to be fair
Reply 32
Yeah was quite a hard paper


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Reply 33
I thought using the Derby vodka thing was quite funny for a rationale; it was a good question though - 2methylpropan-2-ol?

n=[210-(6x12+8x1.01+7x16)]/18.02 or something like that giving 0.99 which rounds to 1.
(edited 10 years ago)
Reply 34
I put 1,1-dimethylethanol but now I think about it it's obviously wrong. Oh dear.

EDIT: http://en.wikipedia.org/wiki/Tert-Butyl_alcohol
(edited 10 years ago)
Reply 35
Also the dehydrating agent is P4O10 - phosphorus (V) oxide - I'm sure that was tricky for most!
Original post by VSEPR
Also the dehydrating agent is P4O10 - phosphorus (V) oxide - I'm sure that was tricky for most!


dehydrating agent for what, can you remember?
Reply 37
Original post by VSEPR
Also the dehydrating agent is P4O10 - phosphorus (V) oxide - I'm sure that was tricky for most!


Pretty sure you could just use conc sulfuric acid
Original post by Picksel8
Pretty sure you could just use conc sulfuric acid


Yeah I know, that's what I remember putting down I don't recall using P4O10 anywhere.
Reply 39
I used LiAlH4, oops!


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