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Chemistry: Post your doubts here!

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can u please help me sketch that titration curve q1b(iii)
see u have a weak base at first so pH slightly lower than 7 and a strong base so pH will rise up to almost a full 14 at the end when all is in...

curve and tilt the corners of the graph but u get the idea :p
and i missed somehting.... the equilibrium point will be marked with an 'x' in the halfway of the vertical line if needed... here it isn't needed i think.
tell me if u dont get this :)
 

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see u have a weak base at first so pH slightly lower than 7 and a strong base so pH will rise up to almost a full 14 at the end when all is in...

curve and tilt the corners of the graph but u get the idea :p
and i missed somehting.... the equilibrium point will be marked with an 'x' in the halfway of the vertical line if needed... here it isn't needed i think.
tell me if u dont get this :)
i know it should start at 1.94 and end at 14
there should be a vertical line at 10vol added but at what ph should that curve join the vertical line i dont get it and the vertical line should go how much units upwards
 
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i know it should start at 1.94 and end at 14
there should be a vertical line at 10vol added but at what ph should that curve join the vertical line i dont get it and the vertical line should go how much units upwards
it's no hard and fast rule... even the starting point is at 1.94 bcz u calculated it. and u have the equation so u know what ratio of volumes would do the complete reaction but u dont know the pH at which neutralisation is complete so u just have to work with the concept that as it was a weak acid and stronger base, the mid point of the vertical line should be slightly above pH 7 ... and r u sure about the 1.94?? bcz that does not seem like the pH a WEAK acid would have. 1.94 is QUITE acidic.
we only work with the numericals we have and other than that we need to show the right concept and it's done
 
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2) In the preparation of soft margarine, glyceryl trieleostearate
is suitably hydrogenated so that, on average, one of its side-chains is converted into the
CH3(CH2)4CH=CHCH2CH=CH(CH2)7CO2 residue and two side-chains are converted into the
CH3(CH2)7CH=CH(CH2)7CO2 residue.
How many moles of hydrogen are required to convert one mole of glyceryl trieleostearate into the
soft margarine?
A 4 B 5 C 6 D 9

need help with the explaination how do we get to the ans in such questions
 
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Section A question no. 6 i dont know what to do and how to do
 

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section A
question no. 9
question no. 10
question no. 11
Section B
question no. 33
 

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^^^^^
srry for posting many questions at a time
but i am preparing for as at home and need a little co-operation frm the ppl of this site
 
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it's no hard and fast rule... even the starting point is at 1.94 bcz u calculated it. and u have the equation so u know what ratio of volumes would do the complete reaction but u dont know the pH at which neutralisation is complete so u just have to work with the concept that as it was a weak acid and stronger base, the mid point of the vertical line should be slightly above pH 7 ... and r u sure about the 1.94?? bcz that does not seem like the pH a WEAK acid would have. 1.94 is QUITE acidic.
we only work with the numericals we have and other than that we need to show the right concept and it's done
i dont kw i think examiner did a blunder here i dont get the graph at all half equavelnce point equavalence point all are against the rules lets see maybe i have to ratafy it well u can check the ms
 
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the answer is D. Why is C wrong? C and D both have one chiral centre and they both have -COOH group!
 

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this paper is absolutely killing me! ans is D
 

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this paper is absolutely killing me! ans is D

tertiary halogenoalkanes are the ones that only proceed through Sn1 mechanism and Dz the only option which consists of a tertiary halogenoalkane
A and B both are primary ones while C is a secondary one
Just in case if you are unsure about what a tertiary one is :In a tertiary halogenoalkane, the carbon atom holding the halogen is attached directly to three alkyl groups which in this case is (Ch3)3CI
 
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tertiary halogenoalkanes are the ones that only proceed through Sn1 mechanism and Dz the only option which consists of a tertiary halogenoalkane
A and B both are primary ones while C is a secondary one
Just in case if you are unsure about what a tertiary one is :In a tertiary halogenoalkane, the carbon atom holding the halogen is attached directly to three alkyl groups which in this case is (Ch3)3CI

ok got it. i thought SN1 mechanism worked for both secondary and tertiary halogenoalkanes. thats why i couldnt understand how both C and D could be right. :)
 
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Someone plz give the name for As and A A chemistry book

cambride international AS and A level chemistry coursebook by Roger Norris, Lawrie Ryan and David Acaster. Some people use additional books but this one is pretty much enough for our course.
 
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I was doing mcqs from the redspot chemistry Mcqs book and the questions from the 80s & 90s were extremely difficult and they were from p3 p4 mostly. Are they as level questions or a2??
 
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