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    (Original post by cookiemonster15)
    Say you are reacting it with an alcohol, the H fro the alcohol would add to one part of the anhydride to create a carboxylic acid, then the other part would react with
    the remainder to create an ester.

    I don't know if this made much sense...
    Sort of, anywhere I can see a visual representation?
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    (Original post by Super199)
    Sort of, anywhere I can see a visual representation?
    https://www.google.co.uk/search?q=an...TCYVMRiDlPM%3A
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    (Original post by Super199)
    Sort of, anywhere I can see a visual representation?
    http://www.chemguide.co.uk/organicpr...es/oxygen.html
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    Name:  benzene.jpg
Views: 284
Size:  70.7 KB

    Can someone explain how to name the thing i've circled in black?
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    (Original post by Super199)
    Name:  benzene.jpg
Views: 284
Size:  70.7 KB

    Can someone explain how to name the thing i've circled in black?
    N-phenylethanamide
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    (Original post by thehollowcrown)
    N-phenylethanamide
    What about the one under it?
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    (Original post by Jackpalmer1996)
    Think i've just come across it actually, the question where it says if oh- is added to a buffer how does the pH remain constant? If so then yeah my bad, i would just say how the oh- reacts with h+ which cancels out the effect of the base being added and eqm. shifts to rebalance concs.
    Yeh ok cool! Thanks
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    (Original post by Super199)
    What about the one under it?
    hmm i think
    2-hydroxy-2-phenylpropylamine
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    (Original post by Super199)
    What about the one under it?
    is that 2-hydroxy-2-phenyl(-1-) propylamine??? Im not sure?

    Would you have to state where the NH2 group is?/

    Hopefully we won't get something horrific like that!
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    (Original post by thehollowcrown)
    hmm i think
    2-hydroxy-2-phenylpropylamine
    Is it 2 phenyl because it is the second carbon that is attached to the benzene?
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    (Original post by Super199)
    Is it 2 phenyl because it is the second carbon that is attached to the benzene?
    yes
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    Which is more soluble propanone or propan-1-ol and why?
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    Do we need to know the structures of Kevlar nylon 66 and terylene
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    (Original post by Super199)
    Which is more soluble propanone or propan-1-ol and why?
    The alcohol becuase it will hydrogen bond with the water molecules but ketone will not
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    I'm fairly sure it's 1-amino-2-phenylpropan-2-ol since the alcohol group has the higher functional group naming precedence (over amino groups).
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    Hey everyone, I'm heading to school now and I just wanted to wish everyone GOOD LUCK! Even if there are things you keep forgetting, don't panic, it will come to you once you're in the exam! See you guys after the exam....
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    Well I'm not getting into uni after that
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    There goes my university place rip
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    Well that was appalling, pretty sure the only question I knew was the one about the two different types of Stitches
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    :'( Does anyone have the paper?
 
 
 
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