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noo!! i'm surprised how anyone could really like it... it screams bollywood to me... but i guess there is no accounting for taste :P

heyy thankss but i'm all A2 now so.... :P

then we can have a straight carboxylic acid too instead of the branched one (E) .......??

http://papers.xtremepapers.com/CIE/Cambridge%20International%20A%20and%20AS%20Level/Chemistry%20(9701)/9701_w12_qp_42.pdf http://papers.xtremepapers.com/CIE/Cambridge%20International%20A%20and%20AS%20Level/Chemistry%20(9701)/9701_w12_ms_42.pdf In Q5, is it wrong to write just reduction instead...

http://papers.xtremepapers.com/CIE/Cambridge%20International%20A%20and%20AS%20Level/Chemistry%20(9701)/9701_w12_qp_42.pdf http://papers.xtremepapers.com/CIE/Cambridge%20International%20A%20and%20AS%20Level/Chemistry%20(9701)/9701_w12_qp_42.pdf Q4. if we do not branch C as given in the marking...

http://papers.xtremepapers.com/CIE/Cambridge%20International%20A%20and%20AS%20Level/Chemistry%20(9701)/9701_w12_qp_42.pdf http://papers.xtremepapers.com/CIE/Cambridge%20International%20A%20and%20AS%20Level/Chemistry%20(9701)/9701_w12_ms_42.pdf Q4 from this paper made a real mess for me... do...

shouldn't it be (4/3)ln(3x-2) ?? becz the derivative of 3x-2 is 3 right?? so we need to multiply and divide by 3...??

Suggest an explanation for the lack of reactivity of the nitrogen molecule, N2. [1]

if the answer is x<k or x>k+m where k and m are constants and the purpose is that x is lesser than k and x is greater than a number greater than k. this is also a range.... just that it is n the extremes and not between 2 extremes. if instead the inequalities are k<x<k+m then we get the...

it is actually a progressive sort of question... take the square of RHS of identity from ii as the LHS is seen to have been squared....

actually i was going to ask u the same question too... A star syed1995 MustafaMotani u guys have any idea how to do this?? it's Q7 of May/June 2013 Paper 42

okaayy i got the one with H but not the a and b parts.. if alcohols dont react then with which parts of the compound will 3 NaOH react? same with the b part.... ummm are u saying that the phenols and carboxylic acid will react in a and b parts but alcohols won't ?

this has me beat.... it is contradictory. at first i thought maybe bcz of OH or benzene ring the value shifted but even OH cant change the value this much... i really succk big time at nmr..... and i request againn... IF anyone HAS any notes on NMR PLEAAASSEEE post them up and tag me...

what does the OH in the middle of the bond between 2 C in the benzene ring mean??

how many moles of H2 will be produced when 1 mol of this acid reacts with an excess of Na metal ?? the ms says 3 mol .... how?? also .... how many moles of NaOH will react with this acid a) in the cold b) on heating ??

can anyone show me the reaction between phenylamine and propanoyl chloride??

no it's in A2