Unit5/unit 4 chemistry - EDEXCEL June 2012

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  1. James A's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by iesians)
    no ! i know why transition metal and their complexed are coloured.
    i wanna know why are AZO DYES coloured .
    the book just says ..."extensive electron bonding in N=N group'" i dont get it ..?!
    your not required to know why they are coloured. It's not required for our syllabus.

    Sorry if im patronising but you don't need to know. There might be some articles on the internet which could explain it, if your that curious.......
  2. iesians's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by James A)
    your not required to know why they are coloured. It's not required for our syllabus.

    Sorry if im patronising but you don't need to know. There might be some articles on the internet which could explain it, if your that curious.......
    i was just concerned they may ask about it , its okay. i have one more question....why is phenylamine more soluble in water than butylamine..?!

    sorry if im annoying ya
  3. Jukeboxing's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by iesians)
    i was just concerned they may ask about it , its okay. i have one more question....why is phenylamine more soluble in water than butylamine..?!

    sorry if im annoying ya
    ....
    Last edited by Jukeboxing; 17-05-2012 at 20:07. Reason: Misread question.
  4. NutterFrutter's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by Jukeboxing)
    I'm guessing its because phenylamine can form more hydrogen bonds(dimers) with water, as it has an -OH group and an amino group where as butylamine just has an amino group.
    Phenylamine has an -OH group? :lolwut:
  5. iesians's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by Jukeboxing)
    I'm guessing its because phenylamine can form more hydrogen bonds(dimers) with water, as it has an -OH group and an amino group where as butylamine just has an amino group.
    OMG im so sorry i confused you with the question ! i had to ask why is phenylamine LESS soluble than butylamine !! SORRY
    and i think you are confused between phenylamine and phenol....
  6. Jukeboxing's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by NutterFrutter)
    Phenylamine has an -OH group? :lolwut:
    Lol my bad, i was thinking phenol.
  7. Jukeboxing's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by iesians)
    OMG im so sorry i confused you with the question ! i had to ask why is phenylamine LESS soluble than butylamine !! SORRY
    and i think you are confused between phenylamine and phenol....
    In that case, the large non-polarity of phenyl makes it less soluble.

    Sorry about my error earlier.
  8. iesians's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by Jukeboxing)
    In that case, the large non-polarity of phenyl makes it less soluble.

    Sorry about my error earlier.
    so what do we write ..?! that the london forces between phenylamine and water molecules do not release enough energy to break down existing hydrogen bonds between water molecules ??!
  9. Jukeboxing's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by iesians)
    so what do we write ..?! that the london forces between phenylamine and water molecules do not release enough energy to break down existing hydrogen bonds between water molecules ??!
    The benzene rings breaks more H bonds between H2O than are formed between the amino group and H2O, and water molecules disrupt van der waal forces between phenylamine molecules.

    All that is energetically unfavourable, making it less soluble.

    From Chemguide
  10. iesians's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by Jukeboxing)
    The benzene rings breaks more H bonds between H2O than are formed between the amino group and H2O, and water molecules disrupt van der waal forces between phenylamine molecules.

    All that is energetically unfavourable, making it less soluble.

    From Chemguide
    i dont geh it !!
    does the lone pair on Nitrogen atom get involved in benzene's delocalised electron system , and thus strong hydrogen bonds cannot be made between phenylmine and water molecules ....?!!?!
  11. Jukeboxing's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
  12. iesians's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    how do we know if we have to use a burette or a pipette ?! in jan 2012 they asked ..

    what would be the most suitable peice of apparatus to remove 10cm3 of sample form the solution?

    i thought it could be both burette and pipette, but in the mark scheme answer was PIPETTE and BURETTE was in the reject list ..!!
  13. IqraAli's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    Can someone please post the link for the jan 2012 F332 salters B paper pls
  14. NutterFrutter's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by IqraAli)
    Can someone please post the link for the jan 2012 F332 salters B paper pls
    This is the EDEXCEL thread.
  15. iesians's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    why is this thread so DEAD ....?!
  16. James A's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by iesians)
    i dont geh it !!
    does the lone pair on Nitrogen atom get involved in benzene's delocalised electron system , and thus strong hydrogen bonds cannot be made between phenylmine and water molecules ....?!!?!
    the lone pair of the nitrogen atom does get involved in 'activating' the benzene ring, but this in effect makes the nitrogen atom less delta negative, hence less strong hydrogen bonds occur between water molecules.....
  17. iesians's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by James A)
    the lone pair of the nitrogen atom does get involved in 'activating' the benzene ring, but this in effect makes the nitrogen atom less delta negative, hence less strong hydrogen bonds occur between water molecules.....
    ahaan i see someones alive here ... thank you very much, i think i got it ..!
  18. James A's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by iesians)
    ahaan i see someones alive here ... thank you very much, i think i got it ..!
    nice!

    I'm currently doing a little biology revision, but it's nice to ocassionally pop back on this thread to refresh my mind on chemistry.

  19. iesians's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by James A)
    nice!

    I'm currently doing a little biology revision, but it's nice to ocassionally pop back on this thread to refresh my mind on chemistry.

    hmmmm i reckon biology unit 5 ..?!
  20. James A's Avatar
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    Re: Unit5/unit 4 chemistry - EDEXCEL June 2012
    (Original post by iesians)
    hmmmm i reckon biology unit 5 ..?!
    yhh, so much to revise!!

    I'm giving these exams by best shot and after that, I deserve such a nice break!
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