Mark Scheme (Results) January 2023
Mark Scheme (Results) January 2023
Mark Scheme (Results) January 2023
January 2023
Edexcel and BTEC qualifications are awarded by Pearson, the UK’s largest awarding body. We provide a
wide range of qualifications including academic, vocational, occupational and specific programmes for
employers. For further information visit our qualifications websites at www.edexcel.com or
www.btec.co.uk. Alternatively, you can get in touch with us using the details on our contact us page at
www.edexcel.com/contactus.
Pearson aspires to be the world’s leading learning company. Our aim is to help everyone progress in
their lives through education. We believe in every kind of learning, for all kinds of people, wherever they
are in the world. We’ve been involved in education for over 150 years, and by working across 70
countries, in 100 languages, we have built an international reputation for our commitment to high
standards and raising achievement through innovation in education. Find out more about how we can
help you and your students at: www.pearson.com/uk
January 2023
Question paper log number P71887A
Publications Code WCH14_01_2210_MS
All the material in this publication is copyright
© Pearson Education Ltd 2023
General Marking Guidance
All candidates must receive the same treatment. Examiners must mark the
first candidate in exactly the same way as they mark the last.
Mark schemes should be applied positively. Candidates must be rewarded
for what they have shown they can do rather than penalised for omissions.
Examiners should mark according to the mark scheme not according to
their perception of where the grade boundaries may lie.
There is no ceiling on achievement. All marks on the mark scheme should
be used appropriately.
All the marks on the mark scheme are designed to be awarded. Examiners
should always award full marks if deserved, i.e. if the answer matches the
mark scheme. Examiners should also be prepared to award zero marks if
the candidate’s response is not worthy of credit according to the mark
scheme.
Where some judgement is required, mark schemes will provide the
principles by which marks will be awarded and exemplification may be
limited.
When examiners are in doubt regarding the application of the mark scheme
to a candidate’s response, the team leader must be consulted.
Crossed out work should be marked UNLESS the candidate has replaced it
with an alternative response.
/ means that the responses are alternatives and either answer should receive full credit. ( )
means that a phrase/word is not essential for the award of the mark, but helps the examiner
to get the sense of the expected answer.
Phrases/words in bold indicate that the meaning of the phrase or the actual word is
essential to the answer. ecf/TE/cq (error carried forward) means that a wrong answer given
in an earlier part of a question is used correctly in answer to a later part of the same
question.
Section A (Multiple Choice)
A is incorrect because the solids are not included in the Kc expression for this equilibrium
B is incorrect because the solids are not included in the Kc expression for this equilibrium
C is incorrect because the solids are not included in the Kc expression for this equilibrium
B is incorrect because propanone also has the CH3CO group that results in a positive iodoform test
C is incorrect because ethanal also has the CH3CO group that results in a positive iodoform test
D is incorrect because both ethanal and propanone have the CH3CO group that results in a positive iodoform test
sodium thiosulfate reacts with the iodine formed (1) Accept equation
S2O32− + I2 → S4O62− + 2I−
when (all) the sodium thiosulfate is used up has reacted Allow a blue-black colour forms at the end of the
the iodine reacts with the starch giving a blue-black colour reaction
(1) Allow iodine reacts with the starch giving a blue-black
colour
Allow blue or black for blue-black
Ignore reference to the colour of the solution before the
starch-iodine complex forms
Do not award iodide reacts with starch
the reciprocal of the time taken for the blue-black Allow 1/t = rate of reaction / 1/t ∝ rate of reaction
colour to appear is a measure of the rate (1) Allow [reactant]/t ∝ rate of reaction
Do not award thiosulfate as a reactant
values of three powers (including [H+] not shown ) (2) Rate = k[H2O2(aq)][I−(aq)][H+(aq)]0
Accept Rate = k[H2O2(aq)][I−(aq)]
For M2 deduct a mark for each incorrect power (reactant
not shown order = 0)
Overall mark for some of these responses including M1:
Rate = k[H2O2(aq)][I−(aq)][H+(aq)] scores (2)
Rate = k[H2O2(aq)] scores (2)
Rate = k[I−(aq)] scores (2)
Rate = k[H2O2(aq)]2[I−(aq)] scores (2)
Rate = k[H2O2(aq)][H+(aq)] scores (1)
Rate = k[I−(aq)][H+(aq)] scores (1)
IP3 lactic acid formed in muscles contains one type of Allow lactic acid formed in muscles contains more of
enantiomer one enantiomer (than the other)
and Allow isomers / molecule for enantiomers
lactic acid formed in the synthesis contains equal numbers of Allow just ‘forms a racemic mixture’
moles of the two enantiomers Do not award laboratory lactic acid and muscular lactic
acid are different molecules
IP4 the carbonyl group is planar Allow ethanal is planar about the carbonyl group /CHO
do not award just ‘ethanal is planar’
do not award intermediate / carbocation is planar
IP5 (in the synthesis the) nucleophile / CN− attacks (equally) Allow nucleophile / CN− attacks from either side / both
from above and below the plane (of the carbonyl group) sides / top & bottom
Do not award SN1 / SN2 / nucleophilic substitution
IP6 (because) lactic acid formed in muscles involves the Allow the enzymes involved (in forming lactic acid in
oxidation of an enantiomer in a way that does not involve the muscles) are stereospecific
chiral centre Allow enzymes react with (only) one enantiomer
Allow biochemical / natural processes (often) select
one particular enantiomer / (optical) isomer
Question Answer Additional guidance Mark
number
18(b)(i) An diagram showing Example of polymer (2)
Allow
C H3 O
CH O C
C CH O
O C H3
(relative peak area) shows 3 times as many Accept 6 protons in one environment and 2 in the other
protons in one environment compared with the Ignore 3 protons in one environment and 1 in the other
other (1)
splitting shows that the two proton Allow the two types of proton are on neighbouring carbon atoms
environments are adjacent (1) Allow doublet must be adjacent to one proton and quartet must be
adjacent to three protons (Do not award omission of doublet and
quartet)
Ignore references to chemical shifts
Ignore explanations of the splitting patterns even if incorrect
structure of lactide
intermediate with negative charge on O atom Allow charge on bracket around intermediate
Do not award intermediate with δ−
lone pair on oxygen
curly arrow from ( lone pair on) oxygen to Allow curly arrow to + on hydrogen
hydrogen ion Allow curly arrow to hydrogen on H─Cl with curly arrow
from H─Cl bond to chlorine or just beyond
Do not award curly arrow from negative charge on oxygen
final product Ignore connectivity errors on groups
Example of mechanism
δ+ δ-
:
:
Question Answer Additional guidance Mark
number
19(c) An explanation that makes reference to the following (3)
the C=O bond is polarised by the (electronegative) Allow ‘the C=O bond is polar / has a permanent dipole’
oxygen atom (1) Ignore just ‘in C=O bond C is δ+ and O is δ−‘
Ignore diagram of dipole shown
Ignore explanations of polarity of C=O even if incorrect
Ignore just ‘π bond is polar’
H− is are attracted to the δ+ carbon (1) Allow nucleophiles are attracted to the δ+ carbon
the C=C bond is non-polar Allow C=C has electron density equally distributed
Ignore just ‘π bond / alkene is non-polar’
OR
nucleophiles are / H− is repelled by (π electrons of) C=C (π electrons) attract electrophiles
C=C (1)
Allow ‘alkene double bond’ for C=C
Allow ‘not attacked’ for ‘repelled’
Ignore references to dipole-dipole interaction
Ignore reference to bond strengths
(Total for Question 19 = 8 marks)
Question Answer Additional guidance Mark
number
20(a)(i) In parts (i), (ii), (iii) and (iv) penalise omission of or (2)
incorrect units once only
Allow units in any order Allow (e.g.) J/K/mol
Do not award J/K mol
Positive signs are not required
Ignore SF except 1 SF throughout (a).
Example of calculation
substitution of values into ΔSosystem = 229.5 + 219.5 − 310.1
ΔSosystem= Sproducts–Sreactants (1)
.
= = 0.096939 / 9.6939 x 10−2(mol dm−3)
rearrangement to make [H+] subject of equation (1) [H+] = √(1.38 x 10−4 x 0.096939)
TE throughout but
Do not award M4 unless there is some calculation to
give a value for [H+]
Do not award M4 if pH ≤ 1 or ≥ 7
Ignore SF except 1 SF
Question Answer Additional guidance Mark
number
21(b)(i) An answer that makes reference to the following (2)
phenol red changes colour in the vertical section of the Accept the colour change of the indicator occurs over
titration curve (1) the course of the addition of a very small volume of
NaOH . Allow any indication of very small volume
calculation of excess amount of sodium hydroxide 3.675 x 10−3 − 2.4235 x 10−3 = 1.2515 x 10−3 (mol)
added in the titration (1) Allow this mark even if it gives acid in excess
Correct answer with some working scores (5)
TE at each stage but do not award M5 if pH ≤ 7
If scaling omitted pH = 11.097 scores (4)
Question Answer Additional guidance Mark
number
21(c)(i) An answer that makes reference to the following General answer in terms of HA and A− scores max 3 (M2, (4)
M3 and M4). Accept names or formulae
gluconic acid and sodium gluconate present (in the Accept RCOOH and RCOO− / RCOONa
buffer) in high concentration (1) Allow large amount / large excess / form a reservoir
Ignore conjugate base
When acid is added Allow forming RCOOH / gluconic acid for protonated
the RCOO− / RCOONa is protonated (1) Allow H+ ion is removed from the solution
Allow RCOO− + H+ → RCOOH
Allow RCOO− + H+ ⇌ RCOOH shifts to the right
When alkali is added the RCOOH reacts Allow alkali reacts with RCOOH forming RCOO- or
and RCOO(−)Na(+)
removing the OH− ion (from the solution) (1) Allow OH− reacts with H+ and RCOOH dissociates to
replace the H+
Allow RCOOH + OH− → RCOO− + H2O
Allow H+ + OH− → H2O and
RCOO− + H+ ⇌RCOOH shifts to the left
substitution of values
and . .
calculation of [RCOO−] = moles required (1) [RCOO−] =
.