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june 2007 ques4 plz sumbody explain da shape ov d orbital in dis one? i mean it says draw one dprbital in each ov two groups? i dunt get da ques :S
acids never give a positive iodoform test!guys, will ch3cooh give a positive iodoform test ? cause well we still have ch3 and C double bond O.. so shouldn't it? :/
those electrons in those particular orbiitals are repelled .. this is the 2 goup one .. so they have higher energythnks n can yuu plzz explain da nxt part in which it says which has higher energy 2 orbital group or 3 orbital?
Yes it is the proper formulasmzimran bro, the ph= pka + log(salt/acid) is this like a proper formula?
Also, do we take the MOLES of salt and the acid or the CONCENTRATION?
Not now, kinda busy with maths s1, have paper in a few hours!smzimran thank you brother, can you explain to me the logic behind question number 5 part iii? marking scheme says that many people got it wrong so it might also help out others! http://www.xtremepapers.com/papers/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_s10_qp_41.pdf
Page number?coursebook cIE....
smzimran thank you brother, can you explain to me the logic behind question number 5 part iii? marking scheme says that many people got it wrong so it might also help out others! http://www.xtremepapers.com/papers/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_s10_qp_41.pdf
(b) Phenylamine, like phenol, can be involved in electrophilic substitution with bromine. The product, 2,4,6-tribromo-phenylamine, is also a white precipitate. So the test can be carried out using bromine water. Phenylamine reacts to decolourise the solution and form a white ppt. while amino-cyclohexane does no reaction.http://www.xtremepapers.com/papers/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_w08_qp_4.pdf http://www.xtremepapers.com/papers/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_w08_ms_4.pdf Q6(b) (c) (d) people help me out with this and suggest me how to do these kind of qs...?
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