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AQA A-Level Chemistry Paper 2 - SOLUTION BANK (Q+A)

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also for this one "In step 3, other aromatic products are formed as well as paracetamol
8.3. Draw the structure of one of these other aromatic products."

I drew a compound with a peptide link .... not an ester but i had no idea what to do so im probably wrong
Reply 21
which question are you referring to?

If you know an answer feel free to post!
Original post by justme2001
The reaction was actually with ammonium ethanoate not ammonia so the formula would have been CH3CONH4

Which would produce the correct thing on the right hand side
Reply 22
I think there is more than one right answer :smile:
Original post by Dreametuber
also for this one "In step 3, other aromatic products are formed as well as paracetamol
8.3. Draw the structure of one of these other aromatic products."

I drew a compound with a peptide link .... not an ester but i had no idea what to do so im probably wrong
Reply 23
Added a poll. Just me who thinks questions are a bit flaky? :confused:
Original post by ÷by0
Building a solution bank of all the questions/answers.

If you can remember a specific question that has not been contributed, please add it down below. Thank you in advance :five:

Question 1
1. This question is about amines.
1.1. Give an equation for the preparation of 1,6-diaminohexane by the reaction of 1,6-dibromohexane with an excess of ammonia. (2 marks)

Spoiler


1.2. Complete the mechanism for the reaction of ammonia with 6-bromohexylamine to form 1,6-diaminohexane. (2 marks)

Spoiler


Suggest the structure of a cyclic secondary amine that can be formed as a by-product in this reaction. (1 mark)

Spoiler


1.3. 1,6-diaminohexane can also be formed in a two-stage synthesis, starting from 1,4-dibromobutane.
Suggest a reagent and a condition for each stage in the alternative synthesis.

Stage 1

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Stage 2:

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Question 2
deduce formula of carboxylic acid, high res mass spec.

Question 3
golf balls.

Question 4
4. Substances P and Q react in a solution at a constant temperature.
The initial rate of reaction was studied in three experiments by measuring the change in concentration of P over the first 5 seconds of the reaction.
The data obtained are shown in table 1.
Q4 Table 1 .png
4.1. Complete Table 2 to show the initial rate of reaction of P for each experiment.

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4.2. Calculate the order of reaction with respect to P and Q.

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Question 5
The rate constant, k = Ae-Ea/RT
For this reaction at 25ºC, k = 3.46x10-8 s-1
The activation energy Ea = 96.2 kJ mol-1
The gas constant R = 8.31 J K mol-1

Calculate a value for the Arrhenius constant A for this reaction. Give the units for A.

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Question 6
6. Compounds A and B both have the molecular formula C4H8Br2 . A has a singlet, a triplet and a quartet in its H1 NMR spectrum. B has two singlets in its H1 NMR spectrum

6.1. Draw the structure of A and B.

Question 7
7.
Isomer X Isomer Y
pentanone.png pentol.png
7.1. Give the IUPAC name of isomer X. (1 mark)

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7.2. Explain how and why isomers X and Y can be distinguished by comparing each of their:



Boiling points
[list]

C13 NMR spectra
[list]

IR spectra

Use data from Tables A and C in the data booklet in your answer. (6 marks)

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Question 8
8. Paracetamol is a medicine commonly used to relieve mild pain traditionally paracetamol has been made in industry in a 3-step process.

8.1. Name the mechanism of the reaction in step 1

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8.2. Complete the equation for the reaction in step 2.

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In step 3, other aromatic products are formed as well as paracetamol
8.3. Draw the structure of one of these other aromatic products.

Spoiler


Chemists have recently developed a two step process to produce paracetamol from phenol. In the first step phenol is oxidised to Hydroquinone.

Spoiler



In the second step hydroquinone reacts with ammonium to form paracetamol. complete the equation for the second step.

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Question 9

Question 10

Question 11

Question 12
12. This question is about chromatography.
12.1. Suggest why 2 solvents were used. (2 marks)

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12.2 Deduce the minimum number of amino acids present. (1 mark)

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12.3. How can the spots be located?

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12.4 peptide chain hydrolysis.

Question 13

13.
13.1 Add H bonds to the diagram

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13.2
13.3 Explain what is meant my the term complimentary in the context of DNA. (2 marks)

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hi!
are these all the questions that came up?
(edited 4 years ago)
Original post by Zahra166
hi!
are these all the questions that came up?

if your asking because you have an upcoming mock ... it won't be this paper
Original post by medic_wannabe
if your asking because you have an upcoming mock ... it won't be this paper

It is this paper for my mocks
Original post by Zahra166
hi!
are these all the questions that came up?

I think they've missed out loads of questions
Reply 28
Has anyone got the paper with them
Reply 29
Original post by medic_wannabe
if your asking because you have an upcoming mock ... it won't be this paper

Have u got the paper on u
Original post by Aran4113
Have u got the paper on u

no, its not released yet. revise for your mocks to gauge how you are actually going to do in the summer

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