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OCR A2 CHEMISTRY F324 and F325- 14th and 22nd June 2016- OFFICIAL THREAD

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Original post by Jehaan
I did a legacy paper and I think the answer said that it can't be split as it can't split itself if that makes sense


Split by the ch3 into a quartet

But not split by the ch2 as the env is identical
Original post by Chem1stry101
Split by the ch3 into a quartet

But not split by the ch2 as the env is identical


Ah I forgot about the CH3 thanks!
Original post by Jehaan
No


Can't be reduced by NaBH4, but can be reduced by other reducing agents
Reply 1463
quick question when oxidising an aldehyde to a carboxylic acid do you have to heat under reflux???
Good luck tomorrow with F324. I won't see the paper till Wednesday but will let you know what I think then
How is everyone feeling about this exam? I've being doing some last minute questions from the revision section on physics and maths tutor and it seems to be going pretty well, I think tomorrow I may go through a couple more NMR q's just before the exam as it seems to always be worth a ton of marks.
Original post by SI 1
quick question when oxidising an aldehyde to a carboxylic acid do you have to heat under reflux???


Yes.
Original post by GEEKSruletheworld!
Can carboxylic acids be reduced by NABH4 aswell?


no
Original post by rahma1994
also, do aromatics have a splitting patters?


yes
Original post by yoda123
Do u use pencil for displayed formula, skeletal, etc and do you have to use pencil


i use pen
Original post by Chem1stry101
Good luck tomorrow with F324. I won't see the paper till Wednesday but will let you know what I think then


are u that guy from twitter
Reply 1471
giys i know this has been asked before but is the hydrogen in the aldehyde can it produce splittings?


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(edited 7 years ago)
Original post by yoda123
are u that guy from twitter


Nope - not a guy ;-)
Original post by ranz
giys i know this has been asked before but is the carbon in the aldehyde can it produce splittings?


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Carbons don't split at all
Reply 1474
Original post by Chem1stry101
Carbons don't split at all


i mean hydrogen


Posted from TSR Mobile
Predictions from @ChemistryALevel
TLC/gas chromatography with nature of solubility is due.
Nucleophilic addition
C13 NMR
benzene ring structure
D2O
Triglycerides
Acid anhydrides
Synthesis always
Chiral C mirror images drawing in 3D
Phenol
Benzene ring structure, what does that mean :/
i think like c-c bonds same length, enthalpy of hyd lss exothrmic than expected, lower electron density and more stable so wont polarise br2 unless in presence of halogen carrier, pi electrons delocalised
bits on the 2 benzene rings that arent bonded to anything so 3+4
hey i remember u, good luck!
(edited 7 years ago)
Anyone know the conditions for coupling (like Phenol + diazonium)? It doesn't say in the book for some reason.

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