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Aqa chem4 15th june 2011 (resit) thread

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Reply 1040
Original post by Zakir
Oh ok...
Yeh thats what i got...the bromosomething purple and yellow, thats gd! :smile:


Did you put purple AND yellow or purple TO yellow? Cos' it said colour change? :s-smilie:
Reply 1041
Original post by sam_xo
Did you put purple AND yellow or purple TO yellow? Cos' it said colour change? :s-smilie:


i put between purple and yellow omggggggggggggggg fail ahahaha
Reply 1042
Original post by T-Toe
I got bromosomething too.

What did you get for molecular ion? m/z=177?


i got C6H5(BENZENE)COOCH2CH3 with another CO on the other branch and the free radical was OCH2CH3 < realised when i was checking through my work that i missed the 'O' so corrected it in time...

what about you?
Reply 1043
Original post by Zakir
i got C6H5(BENZENE)COOCH2CH3 with another CO on the other branch and the free radical was OCH2CH3 < realised when i was checking through my work that i missed the 'O' so corrected it in time...

what about you?


I did all that but accidently inculded another O to the molecular ion :mad:

ffs
Reply 1044
Original post by bjparmar
i put between purple and yellow omggggggggggggggg fail ahahaha


LOL No don't go off what I say! You might be right :smile:
Reply 1045
Original post by sam_xo
LOL No don't go off what I say! You might be right :smile:


You are right.

*awkward silence*

How many marks was that question?
Reply 1046
Original post by T-Toe
I did all that but accidently inculded another O to the molecular ion :mad:

ffs


ohhh ok...mistakes happen, specially under exam pressure...
Reply 1047
Original post by T-Toe
You are right.

*awkward silence*

How many marks was that question?


It was 1 mark wasn't it? :smile:
Reply 1048
Original post by sam_xo
It was 1 mark wasn't it? :smile:


I could've sworn it was 2 marks.
Reply 1049
Original post by T-Toe
I could've sworn it was 2 marks.


Wasn't it 1 for the indicator then 1 for the colour? I'm sure it was one. Lol plus I don't think that type of question would be 2 anyway. Similar questions in some of the past papers from the old spec award 1 mark :smile:
Reply 1050
Original post by sam_xo
Wasn't it 1 for the indicator then 1 for the colour? I'm sure it was one. Lol plus I don't think that type of question would be 2 anyway. Similar questions in some of the past papers from the old spec award 1 mark :smile:


Niice, 1 mark ain't no biggy then :smile:
Reply 1051
Original post by T-Toe
Niice, 1 mark ain't no biggy then :smile:


Yep :smile: Unlike the 6 mark one I got COMPLETELY wrong. Lol :frown:
Reply 1052
Original post by sam_xo
Yep :smile: Unlike the 6 mark one I got COMPLETELY wrong. Lol :frown:


Benzen ene benzene is -120kj mol-1
so we'd assumed that a benzene triene would be -360KJ mol-1 (3x-120)
However benzene have a enthaply change of about -220 KJ mol-1 (forget the exact enthaply change)

Therefore benzene is more stable than benzene triene.

Did you mention any of this? :smile:

It was 6 marks and I'm not sure what else to add..so I also think I've lost marks too :|

edit - I added equations too
(edited 12 years ago)
Damn! I just realised I put Na2CO3, not NaH!
Reply 1054
Original post by JK471993
Damn! I just realised I put Na2CO3, not NaH!


for what?
Reply 1055
Original post by Ramses II
I did NaHCO3 for the acid, causing CO2 effervescence.
For the Acyl chloride, there is a vigorous reaction and white precipitate with AgNO3.
Primary alcohol I did acidified K2Cr2O7, orange to green.


I didn't say vigorous reaction, just white preciptate is formed will I lose the mark?
Original post by T-Toe
for what?


The test for carboxylic acids. Nevermind. I still described the observations :smile:
Reply 1057
Original post by T-Toe
Benzen ene benzene is -120kj mol-1
so we'd assumed that a benzene triene would be -360KJ mol-1 (3x-120)
However benzene have a enthaply change of about -220 KJ mol-1 (forget the exact enthaply change)

Therefore benzene is more stable than benzene triene.

Did you mention any of this? :smile:

It was 6 marks and I'm not sure what else to add..so I also think I've lost marks too :|

edit - I added equations too


The enthalpy of hydroegnation of benzene was more stable due to the identical carbon-carbon bonds in benzene, meaning there is an unused p orbital.

There are 6 delocalised electrons in benzene, which therefore increases the stability of benzene due to the increased delocalisation energy it exhibits.
Original post by T-Toe
I didn't say vigorous reaction, just white preciptate is formed will I lose the mark?


I doubt it :smile:. That is just a hunch though.
Reply 1059
Original post by shak2345
The enthalpy of hydroegnation of benzene was more stable due to the identical carbon-carbon bonds in benzene, meaning there is an unused p orbital.

There are 6 delocalised electrons in benzene, which therefore increases the stability of benzene due to the increased delocalisation energy it exhibits.


was that all that you had to mention?

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