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Chemistry Unit 2 Edexcel, Exam- 23rd May 2012

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Reply 960
Original post by AmrinderRai
Yaay thanks :biggrin:
Instead of transition state... the first step of Tertiary & Secondary Alcohol substitution is the 'rate determining step' instead ?? :smile:


Yesssss not problem

But not 100% about the RDS - i thought that is A2


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Reply 961
Original post by YellowAndBlack
Sn2 also requires a carbocation

Sn1
And is also techniqually a swap
You break off the C-Halogen bond for example - Let's say bromine = Forming a carbocation
A :Nu (nucleophile) attacks and attachs onto this carbocation - bromine is a product

And for Sn1 why are they less stable?


Because its something along the lines of

The charge on the carbon is high

Whereas on tertiary - the methyl groups have a positive effect on the central carbon making it less prone


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Original post by EffKayy
Good luck =)
Thanks for coming on scriblink (!)
k.


no problem =D
Good luck!
Reply 963
When do you use methyl orange and when phenalphthalein?
and methyl orange end point is red -> orange and phenalphthalein is colourless to pink/purple?
Really hope this is a nice paper..
Reply 964
Original post by 2006019
When do you use methyl orange and when phenalphthalein?
and methyl orange end point is red -> orange and phenalphthalein is colourless to pink/purple?
Really hope this is a nice paper..


In alkali

Methyl orange goes from yellow to orange

In acid

It is red to orange

phenolphthalein is pale pink in acid and colourless in acid - to pale pink

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(edited 11 years ago)
Reply 965
Does anyone have the unofficial mark scheme for the edexcel chemistry unit 1 paper sat last week?
Reply 966
Original post by VRS
In alkali

Methyl orange goes from yellow to orange

In acid

It is red to orange

phenolphthalein is pale pink in acid and colourless in acid - to pale pink

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Thank you!
oh my god this is soo hardd
Reply 968
Original post by AmrinderRai
Yaay thanks :biggrin:
Instead of transition state... the first step of Tertiary & Secondary Alcohol substitution is the 'rate determining step' instead ?? :smile:


Just read that sn1 is RDS - two step blah blah blah....

Second attack is fastest so first step is RDH


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is this exam definitely an afternoon exam?
Original post by oli_G
Because at first the barium removes ions from the solution, as it forms barium sulfate - this decreases the electrical conductivity as there are fewer charge carriers.

As more and more barium hydroxide is added more this effect is counteracted by the increase in the number of ions so the electrical conductivity then increases.

Hence, D :smile:


Oh okay thanks!!
Do we need to know major product and minor product??
Reply 972
Original post by itsmehello
Do we need to know major product and minor product??


Its highly unlikely to come up but all you need to know is that the Hydrogen will go to the carbon that already has the most hydrogens (usually the end carbon).
Original post by itsmehello
Do we need to know major product and minor product??


I think so. In one paper we had to recall minor and major from the addition of bromine to propene and we had to show the mechanism for the major product and draw the structural minor product :smile:
(edited 11 years ago)
Reply 974
I'm literally screwed for this exam!
Let's hope there's lots of equilibrium questions in this exam
Original post by lordmackery
Let's hope there's lots of equilibrium questions in this exam


and kinetics :tongue:
Struggling with learning the equations for ozone depletion. -.-
Original post by Exams v__v
Struggling with learning the equations for ozone depletion. -.-


doubt it will come up...its been on in like the last 2/3 exams
Reply 979
What do you think is most likely to come up ? :/

Not looking forward to this exam...:frown:

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