Author Topic: chemistry paper 31 discussions  (Read 1833 times)

Offline Alayna

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chemistry paper 31 discussions
« on: June 03, 2010, 12:38:05 am »
Hey guys..
how did you find the chemistry paper 31?
i found it pretty nice!
what was the answer to why one reaction takes heating and one occours almost spontaniously?
and how about why the cloride compound could not form but iodine compound could?
and why is bromine a licquid and clorine a gas at room temprature?

Offline Aly

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Re: chemistry paper 31 discussions
« Reply #1 on: June 03, 2010, 12:46:12 am »
yeah it was good :)
better than the past pprs atleast :)
i had problems wid the same qns..
i xplained electronegativity for the chloride n iodide qn...donno how far its ryt!
n for y chlorine is a gas n bromine a liquid...i xplained van der waals forces of atraction!

wat dd u rytt?
n u think the thresholds gonna b high?

oh yeah..the oxide was OF2 yeah?

Offline sammwangi

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Re: chemistry paper 31 discussions
« Reply #2 on: June 03, 2010, 01:05:51 pm »
hey!
The paper was ok. I also got F20 for the oxide of the most electronegative element and i also explained the existence of the iodine compund and the non existence of the chlorine compund in terms of the small difference in electronegativity for the Cl and F bt the larger electronegativity difference for the  i anf f hence the compund exhibits enhanced stability.

What did you say fopr the two reactions with NaOH, one was the nucleophilic substitition of a halogenoalkane while the other was the neutralisation reaction of Hcl with NaOH. Why did the hyalegenoalkane need heating while the nuetralisation was almost instantaneous???

 ??? ??? ??? ???
I wrote that the nucleophilic substitutin was endothermic and had a large activation energy hence requires heating inorder to enable the reaction to go on to completion. I then said the neutralisation was exothermic and hence the initial reaction provides enough energy to activate the subsequent reaction as the Ea was small in comparison to the enegy evovled by the reaction... is this ok for the 4 marks... A couple of guys explained it in terms of the existence of the intermediary in the nuclephilic substitution while the nuetralisation was a simple bimolecular reaction. (activated complex theory) 

Help  :-\

Offline rina94

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Re: chemistry paper 31 discussions
« Reply #3 on: June 03, 2010, 01:25:52 pm »
hey guys!
i just wanted to ask which country you live in :)

i hope you all get great grades ;)

Offline leebux101

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Re: chemistry paper 31 discussions
« Reply #4 on: June 03, 2010, 01:48:29 pm »
i wrote about intermediate compounds and activation energy for the 2 reactions...and i also identified them.

and for the chlorine and iodine with fluorine..i wrote abt electronegativity too...

for chlorine and bromine..i wrote abt van der waals forces...

Offline sweetie

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Re: chemistry paper 31 discussions
« Reply #5 on: June 03, 2010, 02:19:19 pm »
okay....

for the Que. about why the organic needs heat while the other reaction doesnt, i wrote that no of electrons in the organic comp. waz more than in HCl so stronger van der waals forces and more energy is needed to break it down and hence begin a reaction ..  :-\

nd ya da oxide waz F2O and guyz hw did u prove in da last Q. that the polycarboxylic acid had 2 carboxyl  groups ???

Offline leebux101

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Re: chemistry paper 31 discussions
« Reply #6 on: June 03, 2010, 03:08:58 pm »
u calculate the moles of each. u will see tht two moles of base are needed for 1 mole of the acid
this means that two OH are needed for neutralizing the acid which means tht 2 acud groups are present

Offline leebux101

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Re: chemistry paper 31 discussions
« Reply #7 on: June 03, 2010, 03:18:49 pm »
and isnt this p21,instead of 31

Offline sweetie

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Re: chemistry paper 31 discussions
« Reply #8 on: June 03, 2010, 03:34:52 pm »
and isnt this p21,instead of 31
ya its p21

Offline leebux101

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Re: chemistry paper 31 discussions
« Reply #9 on: June 03, 2010, 05:25:18 pm »
phew...lol
anyway this ppr was pretty good compared to previpus years...
lets keep the diavussion alive ppl...any more questions..?

Offline joggingday

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Re: chemistry paper 31 discussions
« Reply #10 on: June 03, 2010, 06:25:47 pm »
Yes... how did you draw the molecule of C4H6O5  in the final question.. after finding out that there are 2 carboxylic acid groups present .. how was the molecule drawn? what is its structural formula?

Offline leebux101

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Re: chemistry paper 31 discussions
« Reply #11 on: June 03, 2010, 07:13:41 pm »
i drew the carboxylic acid groups in carbon1 and carbon4 and an OH group at carbon2...
not sure if this is ryt...

Offline sammwangi

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Re: chemistry paper 31 discussions
« Reply #12 on: June 04, 2010, 05:51:04 pm »

HO2C-CH2-CH(OH)-CO2H



I live in Kenya...  :)

Offline leebux101

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Re: chemistry paper 31 discussions
« Reply #13 on: June 04, 2010, 09:34:31 pm »
yeah thts exactly what i did...except i put the OH on the other carbon atom...

Offline Jugular

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Re: chemistry paper 31 discussions
« Reply #14 on: June 04, 2010, 09:42:31 pm »
What happens if I draw the displayed formulas instead of structural? lol