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    (Original post by Suits101)
    For initial rate I said that as the reaction progresses, the concentration of reactants decreases
    Hence initial rate is when time = 0 where the initial concentration of reactants is known so you can find the initial rate at this time

    Initial rate is calculated using the initial rate method;
    Draw a tangent to the curve when time = 0
    Gradient at this point = initial rate for that reactant
    I said at the start - the rate of reaction is the fastest - over time- the concentration of the reactants will decrease so the change will be small? Got it wrong phahah
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    (Original post by lahigueraxxx)
    yeah i think it did
    Keep doubting myself even over the seemingly easy questions, this is too much stress 😂


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    If I just said measure the gradient- would I get one mark?
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    (Original post by SubwayLover1)
    I said at the start - the rate of reaction is the fastest - over time- the concentration of the reactants will decrease so the change will be small? Got it wrong phahah
    Why did you get it wrong?
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    (Original post by bluhbluhbuh)
    18:30- Updated- Version 2

    18:12 Attempting version 1 of the unoffical mark scheme, will keep quoting this for others to see, may even start a thread. Please contribute i will update frequently before i start studying for my bio exam day after tomorrow heh rip

    Misc: tell me where these go!!!

    Equation representing ethanoic acid as a base with nitric acid:
    CH3COOH + HNO3 -> CH3CO+NO3- + H2O

    Identify what reagents are needed to distinguish between the two chlorine molecules, incl. observation. (Acyl chloride vs haloalkane (?))
    Reagent: water/AgNO3 (?)/named carbonate
    Observation: HCl fumes/White ppt./Effervescence -for the acyl chloride.

    Which Nitrogen acts as a stronger base a vs. b (where a is attached to the benzene, and b is a tertiary amine) and why?
    Nitrogen b due to the positive inductive effect of the carbons on the nitrogen, therefore making the lone pairs more available. Consequently nitrogen a is joined to a benzene so the lone pair delocalises into the benzene ring.

    Order of reactions:
    D 1
    E 2

    What is a racemic mixture?
    Mixture containing equal quantities of each enantiomer.

    How to distinguish between the two:
    Expose to plane polarised light, rotates in opposite directions

    Chiral Carbon relationship:
    They are both mirror images of each other/enantiomers.

    4.
    Electrophile structure: CH3C(+)O

    Reaction mechanism:
    Arrow from benzene ring to C+ in CH3C(+)O, then arrow from hydrogen attached to the same carbon as the CH3CO back into the incomplete benzene ring (from carbon 1-4 i believe).

    5. Can't remember exact questions, let me know i'll update ! =)
    Notes:
    Zwitterions have R-N(+)H3 and a COO-
    Hydrogen bond between two amino acids: presumably show any partial bond from one hydrogen on one amino acid to either the nitrogen or oxygen on the other.
    Dipeptides- essentially amides formed from 2 amino acids.

    Advantage of using the polyester suture rather than the polyalkene?
    the ester bond in polyester can hydrolyse whereas polyalkene C-C, C-H bonds are too strong thus cannot. Therefore the former can dissolve naturally whereas the former would require manual removal.

    7. Conc. Of propanone increases by 100, What is the new rate equation and explain pls:
    rate = k[H+]Due to the large excess of propanone, it is no longer affecting the rate as only the H+ concentration limits the speed at which the reaction proceeds.

    Why is the initial rate of the reaction used to determine the order of the reactants rather than at any other point during the reaction? Or something
    Initial rate takes into account the initial concentration of the reactants which is more accurate since, as the reaction proceeds the concentrations of the different species change. (?)

    How do you calculate the initial rate of the reaction from a graph of concentration against time?
    Calculate the gradient of the tangent to the slope. (?)

    8. Organic synthesis to produce the branched primary amine:
    Structure: Same as previous however Br is substituted with CN
    Step 3: KCN w/ ethanol (?)
    Step 4: H2/Ni, LiAlH4

    Question 9 Notes (I don't even need to say the question, everyone knows this question by the number... eek)
    Potassium dichromate turns green, either a primary or secondary alcohol, or aldehyde
    O-H absorption in the Mass spec
    O-H in NMR spectrum, singlet obvs
    CH3-O present in NMR spectrum, singlet
    RCH2 in NMR spectrum, triplet ?
    R(CH3)2 in NMR spectrum, doublet ? uh pls halp don't remember values
    Hi thank you for doing this! if possible could you add in the marks for the questions so i can estimate how badly i did.. also i dont remember a question about how to distinguish between enantiomers?? Did i miss this??
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    For anyone else that found today's paper harder than expected

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    (Original post by DDan123)
    Keep doubting myself even over the seemingly easy questions, this is too much stress 😂


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    haha don't worry I am too, I honestly think I've definitely dropped about 16/17 marks, and then some
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    Wait did they ask us how to distinguish between the enantiomers because I didn't see that?


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    (Original post by 🙈🙈🙉🙊)
    Hi thank you for doing this! if possible could you add in the marks for the questions so i can estimate how badly i did.. also i dont remember a question about how to distinguish between enantiomers?? Did i miss this??
    (Original post by Mo2351)
    Wait did they ask us how to distinguish between the enantiomers because I didn't see that?Posted from TSR Mobile
    That question was NOT on the paper.

    Don't worry, when I read that post I also had a mini heart attack.
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    https://www.facebook.com/groups/148389988911787

    Join this, many people have already and we need to show AQA that this exam was injust in every respect.
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    (Original post by Mo2351)
    Wait did they ask us how to distinguish between the enantiomers because I didn't see that?


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    No they didn't. Don't believe anyone who says there was.

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    (Original post by Boundless_x)
    For anyone else that found today's paper harder than expected

    ur image dont work
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    (Original post by Boundless_x)
    For anyone else that found today's paper harder than expected

    hahah i don't even know why I'm on here anymore, I need to prepare for Bio 4, think I've lost my mind a little today...
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    (Original post by Suits101)
    That question was NOT on the paper.

    Don't worry, when I read that post I also had a mini heart attack.
    Thank you!! at least havent lost those marks...
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    (Original post by lahigueraxxx)
    yeah i think it did
    I think it asked for the section of the polymer not the dipeptide
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    (Original post by lishakb97)
    I think it asked for the section of the polymer not the dipeptide
    What did it ?!?!?! That was not made clear at all
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    Did anyone else not finish the paper ? and how many marks do you think you missed out on missed Q's ?
    Just wondering
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    (Original post by Rabadon)
    ur image dont work
    thats weird what about now?

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    (Original post by rimstone)
    Did anyone else not finish the paper ? and how many marks do you think you missed out on missed Q's ?
    Just wondering
    Guys - I need an A* but I think I have dropped 15-20 marks? No hope!
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    (Original post by Suits101)
    Why did you get it wrong?
    I said if the reaction is endothermic or exothermic the temp will change which will affect the rate,pretty sure I got it totally wrong tho
 
 
 
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