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Cape Chemistry 2015 U2 p2 Ms

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The document discusses chromatography techniques like thin layer chromatography, column chromatography and gas chromatography. It also talks about the chlor-alkali process and environmental impacts of CFCs and CO2.

The main types of chromatography discussed are thin layer chromatography, column chromatography and gas chromatography.

The main steps involved in the chlor-alkali process are the use of a concentrated NaCl solution, a titanium anode, a diaphragm and a steel cathode. Chlorine gas is produced at the anode and hydrogen gas at the cathode.

022].

2020/CAPE/MS 2015

CARTBBEAN EXAMINATTONS COUNCII,


CARIBBEAI{ ADVANCED PROFICIENCY EXAMINATION@

CHEMTSTRY

UNIT2_PAPER02
MARK SCIIEME

MAY/.TUNE 2O].5

g
'. a'.. ::" lr
.. l,- ...\'1::;:

1,r,1.,i...;,:

. r',l..ii:lf
r.,i::.:,:$
' 'r:rt'-1,:i',1
..."!::.;i
,$
.:;,
-z- .j:l
:::\
o 22L2O2O / QAEE h"rs / 20 Ls
CIIEMISTRY
UNTT2-PAPER02
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Question 1

Specif,ic objectives: Module: 1 _ l.L, 2-5, 2.3, 2.4,


2.s

(a) (i) KC I'K xsi


cracking (1)
(ii ) vapour passed over cataTyst/
A1zO3/SiOz at 450 oC (1) 2
OR
Thermal Cracking high temperature (>600"C)
(iii) B: methane, cHa (1)
2
c: propene, CHsCH = CH2 (1)/ CH:cgcgz
NOBE: ft must be condensed foruriI.aei
are both gases and can be either girrea ttre products
(b) (i) o There is the unpairinq of (Ll 2sz electrons aCg or c
(or
tion o 2s2 to the orbi and
e.l-ectron en ters the empt P orbi-tal -
2
o The f, taLs
(1) orbitals sed ve4
(ii1 B.o*ine with propane in sunlight
Iaitiation: a1;Gr ----D Br. + Br. (1)
Ensure fish hook arrow is stroytr

Propagation tr EE
I
C-C
I l^,'--
"E ^ +
E c

E
I
EE
rt .'Ar

I
v
EEf,
tr-c-c-c.
tll + E:Br
ltl
EEE
(1)
BEX
E-c-c
tlt
{_gr.: ar
ltt -c
EEE
(11
IIEEI
* ltl+ +.Br
ttl
-C-C:Br
EEE
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o 22L2O2O /CAPB /MS /2 O 15
CHEMISTRY
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stion 1 cont, d

. . frro etepa ate r€quLred in tlle ptopagatiolr stage,


steps are present and no tisn hook i..o* f..ri-' if-^ two

o If one of the two steps j.s missing


' and fish hook is
missing no marks allotted
Ieraiuation:
.Br + .Br Br3Br
E -..
EE EE EEEE
2a-g-
I
c
lt tt tttt
f, c-c-c
I
E
tt-c.
EE
-+
tt
-c-c
EE
ltlt -c- E

EEES
1)
E EE EEE
a-c I lt ttt
tt-c. 'i.st
c R-C-C-C-Br
-
E
I
EE
ltt
ETE
Any ONE to receive 1 narh
OR
bromine with propene (without sunlight)
EE
tt
E-c-c-c
E

+ Br:/\Br
I
E E
A]1 anrors shouJ.d be
fu.LI arrors and not FISE EOOR (1)

EE l
E-C
tt c
E

+ + :Br'
-C
I
E
(1)

EE E I
lt
E-c-c- I
c f, Br-
tt
EBT
+
+

(1)

E EEI
E
I
c
ttt
I
-c tt
-c -E
E Br Ba
(1)

G
-4- s
o 22L2O2O / CAPE /t{S /2 o1

CHEMISTRY
UNIT2_PAPER02
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OR

UE
ll,/
H-C-C-c
B

+ Br Br (1)
1r
E
n

E E E +

I I I
E c c E + :Br-
I
-c I
+
E Br (1)

The two first steps can'be merfed with the appropriate arrow, one mark for
the direction of each arrow

UE E +

H-C-C
ll I
c E + Br- (1)
ll
H Br
+

u T E
I I I
I
E c c c B
I I I

E Br Br (1)

!,
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o 22L2O2O / CAPE /MS / 201 s
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Ouestion 1 cont'd

KC T'K xs

(iii) Free radi.caL substitution


OR (1) 1
Electrophilic addition,
(c) (i) The reddish brown colour (1)of the bromine is 2
decolourisbd in sunlight (1) -
(ii) The purple colour (1) of the permanganate sol_ution is 2
immediately decolourised / pale pink(1)

Eotal 15 uarks 5 6 4

*
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|22L2O2O/CA.PGArSl2O15
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Question 2

Specific objectives: l{odule: 2 - L-L, 2-2, 2-3, 2.A, 2'5


KC T'K xs
(a) (i) Accuracy

Reading burette at eye levef


Removal-of filter funnel after adding titrant to burette
Reading burette to 2 decimal places (1)
Eliminate any bubbles in bureEte tap
Do not blow out remaining liquid at the tip of the pipette
Overshooting the burette
AnY ONE
1
(ii) Precision:
Adding titrant drop by drop near the end point
Taking successive readings untj-l constant voh:rnes are
obtained
Taking successive readings until the volume does not dj-ffer
by more than 0.1cm3 (1)
Faulty calibration of instrument
If the student answ€trs in the positive or negatine, accept-
Arly oNE 1
(b) o High level of purity (1)
. Atmospheric stability (1)
. Large mofar mass (1)
. Reasonable solubility in titration (1)
. Absence of hydrate water (1)
o Cheap and readily avai-lable Any lIEo (2) 2

(c) (i) Graph: (Page 7)


Draw a curve, (1)
6 accurate points (1) 4
Best fit (2')
Accepted fit - 1 mark onIY
(ii) End point volume: 24-5 + 0-5 (1) 1

(iii) 2'o x 25
25 cm3 NaoH contain
1000
: 0.05 moles (1)
Give the mark for expression NOT the answer.
Moles NaoH: HC[: 1:1
Moles HCL : 0.05
24-5 cm3 HCt contaln 0-05 mol-es (1)
2
0-05x1000
1000 cm3 conEal-n (1)
24 -5
:2.04 M HCI
* Not Earkirrg for unit
-1-
o 22L2O2O I CAPE /Ms / 2 O 1 s
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Question 2 cont'd

KC T'K xs
(d) 25 cm3 NaoH added to a polystvrene cup using a
pipette. (1)
(Sofrrtiot allowed standing for few minutes)and
temDerature noted- (1) 4
ffi acid added from burette, mixture
stirred and temperature noted. (1)
This is:repeated"until a total of 45 sr3 of acid
until the (1) temperature stablised'
"." "aa"a'or

Total 15 marks e 7 4

*
;t.14
a i.il
'.'5i
. l:ii
''Lrt
' ,:, +,#,
1 ii;,l
-8- ttt:
|22L2A2A / CAPE /t{S /2 01 5 '!i

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r..)'iesEion 2 cont'd

.l:;..
LLt-
rp.!r
.*r. l.;.
'-F|-

+*
-l..-

-i_-

I
t
t
a
,.
&
E
u

-l
-f

j-
-i-;
I

32 '-1-r ti i Tl : i].1 i;
.,-:], l.:
.-l-l L- -r- r.J." .1,.1
I,
' ll -! : Ii ri.I.! i/{
.-LL il
!,rt
-l- t --- -r{+
-l+--i-
I
-+, (f) tor 2 ilfutbat llnor
'- rl-.- J -f-1- -;*{-F--i -ilt-ird (l) tor p.tot tG aooutet !tolut.)
--tst-;_ -rln-
'I "-! I ri
..r
(2, b..t llt Lbcr
-' l'l^- -1'1r'
:.f ffi
I il
.l
;- i i -T
.l
ll ,1 I L.
i.
l
i ,...-i +
f !-

---!- . i'f

-F i-'
li

I
ii+f;

33
tlfi
10 ls 30 30
volur of rcld rddod (crt)

*
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o22L2O2O lCAPE/Ms /201 s
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UNIT2-PAPER02
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Question 3

Specifie Objectives: tfioduJ.e: 3 - L.2,7.!, 1.2, 1.3

KC UK xs
(a) Increased pressure/conc. of reactants (X KC)
Decreased temperaFure (1 KC, 3
usd of d catityst' (1 KcI : i

(b) (i) chatelier's Principle: if one or more factors that


rLe:
affect an equilibrium are chanqed, the position of 1
equiltbriurn shift-3 in the direction which opposes
the change- (1 XC)
(ii) . Low terperature (1 UK)
2
o ltigh pressure (1 tII()

(iii) o The sulfur trioxide is dissolved inLo conc. sulfuric


acid to form oleum (1 xS)
. The oleum j.s diluted with water to form conc. sulphuric Z

acid .(1 Iq)


(iv) o HzSOr(/) + Sog(S) -+H2S2or (1)) 2

o HzSzoz(|,) + Hzoot --+ 2Hzsoa(|,) 2

For each :eglll: B;+anced (1) + state .s1mbo1s (1)


If in b(iii) 'studditts"uied sulphuric acid o..r Qi fute sulphuric
acid, state slnnbol for sulphurj-c acj-d must'be ( aq) in part (iv)
(v) Safetyconsiderations
Reaction between SO: and vlater is highly exotherrnic
(1)
Clouds of sulfuric acid are produced. (1)
Sulfuric acid can cause burns Lo the skin and flesh. 3
(1)
sulfuric acid can cause blindness if it gets into the
eyes. (1)
Use of protective gear
Any THREE of. ttre aborTe, 3 x 1

i
I

Eotal 15 marks 4 6 5

:\.

G
. .r;,1:
.:l-:'.i
' I ':ri'ri
. .l : ..':r*41
Ir;r'l;!r:
':;,'ilt
:.,.:;,:il
..: |'.';)
.;:t:ti.
',i:ii.i
'+;,
-10- . ri'
022L2O2O lCAPE /MS/2 O 1 s
CHEMISTRY
UNIT2_PAPER02
MARK SCI{EME

Question 4

Specific objeetives: Modulei L - 4-L, 4.2, 1.?, 4.4, 4.4, 4-5,.4-5


xc I'K xsi
(a) Addition polymerisdtiurr involves the linkinq of cne
type of monomer with double (1) or triple bonds' to
s ive Lhe pollmer as the roduct ( 1):

Condensation polymerj-sation invofves the linking of


two types of monomers oR monomeri wi th biilunctiona:.
two funct onal r (1) to give, thg
4
polymer and a small molecule such as water or
hyd,rogen chloride. (1)
Students must mention the tYPe of bon4- and the
amount of products for EACH tYPe of lrclymerization
to get ttre 4rks

(b) Carbohydrates/Polysaccharides (1)


Proteins (1)
Note: PoJ-yamides cannot be accepted here siace ttrey
include symttretic substances- Polysaccharides are
aII naturally occurring.
€.9-. glycogen
- cellulose 3

starch (1)
pecEin
albumin
keratin
collagen AITY oNE

(c) o o
ll il
DEO CE2CH2- Of, + nEO c --@- c OE
-
ethane':lr 2-dtol beazeDe-I, 4-
dicarboxylic acid
(1) (11
$ 4
o o
il il
o-cEzcB2-o- c
-@- c
(1)

+ ouzo (1)

Studeuts will be penal.ized for NOI insertiag ttre


'rf in ttre lrcIyner onIY.

&
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o 22L2O2O / CAPE /MS/ 201 s
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UNIT2_PAPER02
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Question ,l cont'd

KC UK xs

(d)
The .,Jrink between the two monomers is
OE
ilr
-c-ll-
(1)oR
N
because one end of unit is and
I
f,
'c:
the other end is ll
o
E CE.
The remaining part of repeating
unit has (1).
lt' 1

-E-C-C-
ril
EO
E
and (U giving monomers:
r - cEr- c
I

I
o
cE-
I'
B--;tr-C-C-OE
,lll EO
(1)'
E
I
E-tr-cE--c-oE
'll 4

o (1)

If 'the breaking of C to N bond i.s shot^rn and the monomers


are cortect then the mark awarded is 3 marks- If the
breaking of'the-bbnd is not shown then the mark is two.
lfotal 15 aarks 7 I
OR

If the parts of the polymer are given (the pollmer has been split and the
both halves shown) ,then 1 mk each. The actual monomers shown for each part
of the polymer given wi'll r'eceive Lmk each- 4l'trCs
:: ::.
:.': .il
i!.tiii

,,.iai:

,.:.1"!

-12-
o22L2O 20 / CaPB /Ms / 201 s
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UNIT2-PAPER02
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Questign 5

ipecific Objectives: Modulei 2 - 8.7.t 8-2, 8.3, 8 -4, 8.5, 8-6

KC T'K xs
I

(a) Chromatography involves the separation of components


of a ruixture bet ween two Dhases. (1)
Involves the partitioninq of ts between a
stationarv phase and a mobile phase. (1)

Partitioning occurs because the gomponents of the 4


mixture wiII exp.erience different absorption forces

Have different soi-ubil-itY wi th the mobile phase. (1)


If student stetes o! iuPLies ttrat a uobiJ.e phase aDd a
stationary phase axists - 1Ek
(b) (i) The componen ts can be detected by a reagent calfed
a loca tinq agent or visualiz inq aqent (1) . This
will react with the component and ,!ryg}gg5! 2
compound. (1)
(j-i ) Rr = Distance moved bY solute
Distance moved by solvent (1) 1
If eguation is iupJ.ied give the uark
2.5 1
R. of = 0.2 (1)
' 13.5

t2.5 t-
R-ofR=-=0-9 (1)
' l-3.5

(iii) Rhasa eate ubilit l_n mobile (1)


than Q hasas yto torb onto
the stationarv Phase. (1) oR Q is more Polar so 2
1t is stronglY adsorbed on to the stationarY Phase
than R which is less Polar-
If student says Rr factor of Q and R differ because of
difference in solubilities and differ in ithe levels -of
adsorption onto the stationary phase -€!{EY lEIs
(c) Thin layer chromatograPhY:
Separates smafl amounts of compounds (1)
usla to separate (dyes, aniao acids, plant pignnents) (1)
Less useful if quantificatlon of large amount are 2
required. (1)
Cannot separate compounds of slmilar Rr values' (1)
Sauqlles can be removed fr,lrtL ariilysis' (1)
*
Use (1) + conrnent on usefuJ-ness (1)
,1, . i :ra''

.' ..::i:',.: - 13-


.':.:
l:,;i.,, .::. .t;;:yi:i o 22L2O2O / CAPE /Ms /2 o1 s
;a:. -; CHEMISTRY
-:r'
r;,,=#' UNIT2-PAPER02
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r
ffi

Question 5 cont'd
Specifie Objectirres: t{odul.ez 2 - 8.1, 8-2, 8.3, 8-4, 8.5, 9.6
KC t,K xs
(c) Column Chromatography:

Large anounts of material- can be separated and collected-


(1) 2
Large columns can be'u'sed'for purification- (1)
Can be used to prepare compounds. (1)
Fractions can be collected for'.analysis- 11)

Use (1) + comeat on;usefuJ.liess (1)

ltota1 15 narks 7 I

&
.': . :.

. :. ,: .. '.-il
r

.' .' .' .


::
,: i::':;:.-
::i.,rj
.-.?']
:)ri'
.'(+
1,.i1

-1 4- ,..' j
g22L2O2O ICAPElMS/2O15
CHEMISTRY
UNIT2_PAPER02
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Question 6

Specific Objectives: Module: 3 - 6-L, 6-4, 9-2, 3.3

tRc'' T'K xs
(a) CblorLae E1drogea
4' A
I

I
t I

concentrated
sodiurn
cbloride
solution
3tee1
fitaniu- cathode
anode

Sodiun
Diapbragu solutioD
cotltaEiEated
witb f,aCI
Must be conc sdiu[ chloride or brine
Anode i 2 C/-(aq) - 2e- Clz (S) (1 Kc)
Cathode: 2H* (aq)+ 2e- 4 Hz (S) (1 Kc)

DiagrarnpglY (1 Kc)
Diagran + 2 labe1s (2 Kc) 6
Diagran + 4 J.abels (3 Kc)
Diagram + 5 or Dore labe1s (4 Kc)

to) Health concern-Iink concern wirh its effect 1

Use of asbestos diaphrasm (LKC)


Asbestos deteriorates with use overtime' (t'E) 2
Dry asbestos fibres can be inhaled/ingested causing
respiratorY Problems - (Ix)
Asbestos is considered to be carcinogenic (UK)
Possible leakage of chlorine gas into the environment- 2(LK)
1 KC + anY IIKs

(,
,: "':: ,'

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o 22L2O 20 | CaPE /l,rs /2 01 5
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Question 5 cont'd
KC I'K

(c) (i) Production of CFCs has decl-ined:


It was discovered in the Lg70,s that cFCs accelerates the
depletion of the ozone layer in the atmosphere' (1 ulc)
Destruction of the ozone Iayer allows harmful w radiation (1
3
UX) to reach the surface of the EarLh.
CFC's are broken down in stratosphere to g ive chlori-ne free
radicals which react with ozone to cause its conversion to
oxfi-n-(l tK)
(ii) Products of combustion of fossil fuels - Coz:

COz is a "greenhouse gas" - (1)

Increased concentration of Coz- contributes to the


greenhouse (1) effect i'e' qIobal warming'
3
Negative effect on the atmosphere through melting of
gficiers and ice-caps increase in sea leve1s' (x)

Decreases productivity of the land


SOzTCOTNOz emissions ].ead to acid rain
lltr€lmnEEofttreaborreorsirni].ar-3x1nark

Tota]. 15 uarks 7 I

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