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http://papers.gceguide.com/A Levels/Chemistry (9701)/9701_w15_ms_21.pdfocto nov 2015 mark scheme 21??????
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http://papers.gceguide.com/A Levels/Chemistry (9701)/9701_w15_ms_21.pdfocto nov 2015 mark scheme 21??????
didnt got it.. THanks thoough
You are given this situation:
This was a simple question, let's do a bit tricky question now Consider the question below:
This was a simple question, let's do a bit tricky question now Consider the question below:
You know that the number of moles of Nitrogen, N2, at equilibrium are 2.32mol which are 0.32 moles greater than the number of moles initially. This tells us that, some amount of NH3 has broken down to give this increase in mole of N2 at equilibrium. So by using the mole ratios, find the number of moles of NH3 which have decomposed to give 0.32 mole of N2.
n(N2) : n(NH3) = 1 : 2
^ they are in this ratio, so the moles of NH3 broken are:
0.32 * 2 = 0.64mol
Subtract ^ this amount of mole from the initial number of moles NH3, to find the number of NH3 at equilibrium. 2.40-0.64 = 1.76mol
Now in a similar way, find the number of moles of H2 formed by the decomposition of NH3.
n(H2) : n(NH3) = 3 : 2
so moles of H2 formed = 0.64 * 3/2 = 0.96mol <----- add this amount to the initial number of moles of H2, to find the the no. of moles of H2 at equilibrium: 6 + 0.96 = 6.96mol
Now you have this information:
View attachment 60509
Since the volume is 1dm^3, the conc. of the substances at equilibrium will be equal to the moles of the substances.
Finally use the Kc expression, to get your final answer:
So the answer is A.
No problem
that was awesome!
thank you so much
Can you please post the picture of that question?In the infrared spectroscopy question given at the end of the book (the Roger Norris thing) there's a question which asks to state the three distinct points for indentifying the compound or more generally if theres such a question in which there is only one identifiable peak for say OH group and then other complicated peaks occur in the fingerprint region, what could be the three reasons to state?
It myt come.Should I study infrared spectroscopy if im doing A2? can it come in Paper 4 ? (its a new addition to the AS syllabus)
Man but wtf where do they expect us to learn it.It myt come.
you are right about A and C, but actually ketones have higher boiling points, because they have two alkyl groups on either side of their C=O which makes it more stable. which is why I was confusedI think because the products of A and C are both carboxylic acids, which have hydrogen bonding between their molecules.
There won't be any reaction for B, cause it's a tertiary alcohol.
The product of D is a ketone, which doesn't have hydrogen bonding between its molecules, leading to a lower boiling point?
I'm sorry if I'm wrong. This is probably the first chemistry question I tried in like months...
You are right :3I think because the products of A and C are both carboxylic acids, which have hydrogen bonding between their molecules.
There won't be any reaction for B, cause it's a tertiary alcohol.
The product of D is a ketone, which doesn't have hydrogen bonding between its molecules, leading to a lower boiling point?
I'm sorry if I'm wrong. This is probably the first chemistry question I tried in like months...
Its correct.I think because the products of A and C are both carboxylic acids, which have hydrogen bonding between their molecules.
There won't be any reaction for B, cause it's a tertiary alcohol.
The product of D is a ketone, which doesn't have hydrogen bonding between its molecules, leading to a lower boiling point?
I'm sorry if I'm wrong. This is probably the first chemistry question I tried in like months...
you are right about A and C, but actually ketones have higher boiling points, because they have two alkyl groups on either side of their C=O which makes it more stable. which is why I was confused
Hasn't it got something to do with branching?
But branched also have lower boiling points
get that..thank youYeah, but still no hydrogen bonding which is a strong force of attraction leading to increased boiling points. Absence of it would surely lower the boiling point.
And yes, I think straight chain alkanes have HIGHER boiling points cause of more contact point or something... but the comparison here is clearly because of the intermolecular forces of attraction.
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