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***2013 LC Chemistry Before/After***

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  • Registered Users Posts: 36 mocker2012


    Yeah the sodium dichromate was the problem, carcinogenic or something I think. I'd love if ethanoic or ethanal came up though, theyre grand plus handy enough calculations. Don't actually know why I asked, just being nosy + looking for anything to distract me from accounting!:P

    We just went ahead and did those experiments anyway!! YOLO:D


  • Registered Users Posts: 163 ✭✭wow exuberant


    My predictions: Ethanal or ethanoic acid (maybe both)
    The rate of reactions expt with the hydrogen peroxide
    iron Tablets titration


  • Registered Users Posts: 204 ✭✭MarieCurie22


    mocker2012 wrote: »
    We just went ahead and did those experiments anyway!! YOLO:D

    SHHH!The department of education can hear you!!!!


  • Registered Users Posts: 204 ✭✭MarieCurie22


    My predictions: Ethanal or ethanoic acid (maybe both)
    The rate of reactions expt with the hydrogen peroxide
    iron Tablets titration

    Just because they came up on the DEB mock :P
    Iron Tablets or BOD of water (BOD more likely)
    Ethanl or Ethanoic acid
    HCL and NaOH heat of rxn or affect of temp on rate of reaction...


  • Registered Users Posts: 204 ✭✭MarieCurie22


    there is no way in hell theyd ask both not a hope!


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  • Registered Users Posts: 163 ✭✭wow exuberant


    there is no way in hell theyd ask both not a hope!

    they've done it with ethyne and ethene before


  • Registered Users Posts: 163 ✭✭wow exuberant


    Just because they came up on the DEB mock :P
    Iron Tablets or BOD of water (BOD more likely)
    Ethanl or Ethanoic acid
    HCL and NaOH heat of rxn or affect of temp on rate of reaction...

    really lol? I honestly forgot what came up on our pre


  • Registered Users Posts: 204 ✭✭MarieCurie22


    really lol? I honestly forgot what came up on our pre

    Iron tablets came up in 2009, BOD in 2003 i think? only once...so well over due...


  • Registered Users Posts: 46 lizardspock


    mocker2012 wrote: »
    We just went ahead and did those experiments anyway!! YOLO:D

    whoah chem badass over here!!:pac:


  • Registered Users Posts: 90 ✭✭simons545


    Iron tablets came up in 2009, BOD in 2003 i think? only once...so well over due...

    I agree, I think they're worth learning. They were on a mock if I'm not mistaken?
    Anyone else have that woeful company examcraft correcting your mocks?
    They marked 78% on my paper, forgot to add up two sections, didn't mark the answers even though given word for word and totaled near 60 odd marks missing.
    and seriously, what's the deal with having no question numbers in chemistry and physics? You'd think all the "intellectuals" on the board...you can finish that.


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  • Registered Users Posts: 204 ✭✭MarieCurie22


    simons545 wrote: »
    I agree, I think they're worth learning. They were on a mock if I'm not mistaken?
    Anyone else have that woeful company examcraft correcting your mocks?
    They marked 78% on my paper, forgot to add up two sections, didn't mark the answers even though given word for word and totaled near 60 odd marks missing.
    and seriously, what's the deal with having no question numbers in chemistry and physics? You'd think all the "intellectuals" on the board...you can finish that.

    Tbf in chem they do label far better than physics so many times ive skipped questions cause of their inability to label their work! it also must be a nightmare correcting!


  • Registered Users Posts: 90 ✭✭simons545


    Tbf in chem they do label far better than physics so many times ive skipped questions cause of their inability to label their work! it also must be a nightmare correcting!

    Yeah, I feel sorry for the poor examiners. I just put the first word of the question with some ":" after it and double check the questions. (They are colons right?) It just feels weird calling them colons after the biology exam on Friday...Tangent much. Back to the photoelectric effect... hf=...[/I
    I envy the people with two days to study chemistry left...


  • Registered Users Posts: 204 ✭✭MarieCurie22


    simons545 wrote: »
    Yeah, I feel sorry for the poor examiners. I just put the first word of the question with some ":" after it and double check the questions. (They are colons right?) It just feels weird calling them colons after the biology exam on Friday...Tangent much. Back to the photoelectric effect... hf=...[/I
    I envy the people with two days to study chemistry left...
    Not even that most of them had the whole weekend! :(


  • Registered Users Posts: 161 ✭✭Hamza Malik


    Just finished all my organic study :D How are people finding the mechanisms? Tbh I find them an easy 15+ marks ;)


  • Registered Users Posts: 204 ✭✭MarieCurie22


    Just finished all my organic study :D How are people finding the mechanisms? Tbh I find them an easy 15+ marks ;)

    Super bien although watch the wording of the questions sometimes they try trick you...so Hamza enlighten us all :P Cholorination of methane to form chloromethane?


  • Posts: 0 [Deleted User]


    SecondMan wrote: »
    Woah 9%.. There's this guy in my class who comes out of every exam saying "That actually went very good. I'll be expecting at least a C". A week after, out come the results...F's all round. He lets on he's so intelligent. Just before the mocks he was finally persuaded by our Chem teacher to move to ordinary level after various replies back to her such as: "But I'm well able for a C in higher". Turn out he got 19% in ordinary level Chemistry in the mocks.

    Well it's not that this guy thought it went well. He actually finds Chemistry very hard and had a good idea that he failed but he stayed in for 3 hours to try do his best. He stayed at Higher Level and we spent the last 5-6 weeks doing revision so he thinks he'll pass but it's a big step up!


  • Registered Users Posts: 161 ✭✭Hamza Malik


    Super bien although watch the wording of the questions sometimes they try trick you...so Hamza enlighten us all :P Cholorination of methane to form chloromethane?

    Haha this will be good revision. So a CL2 molecule is broken in cl + cl by UV light.

    Cl attacks methane to form Cl-h and methyl free radical.

    The metyl free radical attacks another cl molecule. And causes a chain reaction.. :D

    Oh I forgot to mention it forms chloromethane.


  • Posts: 0 [Deleted User]


    Just finished all my organic study :D How are people finding the mechanisms? Tbh I find them an easy 15+ marks ;)

    I think I'm the only person on boards who NEVER does q8/9 (depending on the year) because I can't understand the mechanisms at all! Or the different chromatographies. I'm hopeless at it! And then they ask for evidence to support it and I get more confused. Not a hope I'll be attempting it on Tuesday.


  • Registered Users Posts: 90 ✭✭simons545


    Well it's not that this guy thought it went well. He actually finds Chemistry very hard and had a good idea that he failed but he stayed in for 3 hours to try do his best. He stayed at Higher Level and we spent the last 5-6 weeks doing revision so he thinks he'll pass but it's a big step up!

    Fair play :) That was a very nice thing to do. Best of luck to him so and to everyone whooooo only 13 hours and 12 mins till physics ahahaha, fml...


  • Registered Users Posts: 90 ✭✭simons545


    Haha this will be good revision. So a CL2 molecule is broken in cl + cl by UV light.

    Cl attacks methane to form Cl-h and methyl free radical.

    The metyl free radical attacks another cl molecule. And causes a chain reaction.. :D

    Oh I forgot to mention it forms chloromethane.

    I think you should use reaction equations bud :)
    You should throw in homolytic fission of Cl2 and the formation of the Carbonium ion. They will prob tie in something to do with bromine water/sodium chloride as well if they ask that tomorrow, so know the three products formed too! Oh and appropriate use of curly arrows!


    Are these the three products formed with the Bromine water solution?
    -1-chloro,2-bromoethane
    -1-chloroethane (or dichloro?)
    -2-bromoethanol

    Tuesday I mean, getting ahead of myself...


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  • Registered Users Posts: 204 ✭✭MarieCurie22


    I think I'm the only person on boards who NEVER does q8/9 (depending on the year) because I can't understand the mechanisms at all! Or the different chromatographies. I'm hopeless at it! And then they ask for evidence to support it and I get more confused. Not a hope I'll be attempting it on Tuesday.

    Hey I love teaching people stuff especially chemistry :P Ask Hamza....pretty decent too and would love to help you with the organic and mechanisms tomorrow evening?


  • Registered Users Posts: 482 ✭✭woopah92


    To whoever said the need to label the questions better, I agree 10000000%. I got 89% in the mock and I forgot to put in a definition that would have given me an extra 5 marks and 90% all because I didn't see that part of the question. My fault I know, I'm going to triple check all the questions on Tues. :pac:


  • Registered Users Posts: 36 mocker2012


    simons545 wrote: »
    I think you should use reaction equations bud :)
    You should throw in homolytic fission of Cl2 and the formation of the Carbonium ion. They will prob tie in something to do with bromine water/sodium chloride as well if they ask that tomorrow, so know the three products formed too! Oh and appropriate use of curly arrows!


    Are these the three products formed with the Bromine water solution?
    -1-chloro,2-bromoethane
    -1-chloroethane (or dichloro?)
    -2-bromoethanol

    Tuesday I mean, getting ahead of myself...

    Thats evidence for ionic addition not substitution!!!:P


  • Registered Users Posts: 204 ✭✭MarieCurie22


    mocker2012 wrote: »
    Thats evidence for ionic addition not substitution!!!:P

    Evidence for substitution is...
    -The formation of ethane (not present at start)
    -The addition of tetramethyl lead speeds up rxn
    -Only takes place in the presence of uv light!


  • Closed Accounts Posts: 1,696 ✭✭✭outnumbered


    Evidence for substitution is...
    -The formation of ethane (not present at start)
    -The addition of tetramethyl lead speeds up rxn
    -Only takes place in the presence of uv light!

    Check your Skype :P


  • Registered Users Posts: 161 ✭✭Hamza Malik


    simons545 wrote: »
    I think you should use reaction equations bud :)
    You should throw in homolytic fission of Cl2 and the formation of the Carbonium ion. They will prob tie in something to do with bromine water/sodium chloride as well if they ask that tomorrow, so know the three products formed too! Oh and appropriate use of curly arrows!


    Are these the three products formed with the Bromine water solution?
    -1-chloro,2-bromoethane
    -1-chloroethane (or dichloro?)
    -2-bromoethanol

    Tuesday I mean, getting ahead of myself...

    yeah I will. I didn't use them here cause its hard to type them.

    And the products your talking about are from a different mechanism. Your talking about the bromination of ethene.

    I'm talking about cholrination of methane :)


  • Registered Users Posts: 161 ✭✭Hamza Malik


    I hate chromatrography.. can I risk it to leave it out?


  • Posts: 0 [Deleted User]


    Hey I love teaching people stuff especially chemistry :P Ask Hamza....pretty decent too and would love to help you with the organic and mechanisms tomorrow evening?

    Sure I don't mind if you're not too busy :) Just means I can keep my options open in the exam :)


  • Registered Users Posts: 346 ✭✭weirdspider


    simons545 wrote: »
    I think you should use reaction equations bud :)
    You should throw in homolytic fission of Cl2 and the formation of the Carbonium ion. They will prob tie in something to do with bromine water/sodium chloride as well if they ask that tomorrow, so know the three products formed too! Oh and appropriate use of curly arrows!


    Are these the three products formed with the Bromine water solution?
    -1-chloro,2-bromoethane
    -1-chloroethane (or dichloro?)
    -2-bromoethanol

    Tuesday I mean, getting ahead of myself...

    Its actually 1-bromo 2-chloroethane, I like to remember that they are in alphabetical order! And yeah its 1,2 dichloroethane


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  • Registered Users Posts: 346 ✭✭weirdspider


    I hate chromatrography.. can I risk it to leave it out?

    Well paper chromatography isn't too bad! Just put a little dab on ink, put it in acetone and the different components seperate out. But I reckon you could, it only comes up as a tail of one of the choice Qs at the end. But just make sure you're not leaving too much stuff out already, that could be problematic on Tuesday! :P


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