Trial Examination 2010 Chemistry - Paper 2 Answers: Section A
Trial Examination 2010 Chemistry - Paper 2 Answers: Section A
2010
CHEMISTRY – Paper 2
Answers
Section A
1 (a)(i)
(ii)
1+1
(iii) 1+1
_
O
N O
Trigonal planar 1
O
Total 10
2
[H+] = 5 x 10-14
pH = - log 5 x 10-14 1
= 13.3
(c) - NH3 is a weak base and dissociates partially in water. 1
/ The OH- concentration is much less than 0.200 mol dm-3
(d)
14
11.3
End-point
pH
7
Curve 1
| | | | | | Mark 11.3 1
Mark 40, end-point 1
0 10 20 30 40 50 60
3
(e) √ for methyl orangeVolume of added acid / cm 1
(f) NH3(aq) + H2O(l) NH+4(aq) + OH-(aq)
- On adding a small amount of OH-(aq),
NH+4(aq) + OH-(aq) → NH3(aq) + H2O(l)
(added)
Equilibrium would shift to the left to’mop up’ the added OH- ions.
1
- On adding a small amount of acid, the H+ (aq) is removed by this reaction:
H+(aq) + NH3(aq) → NH4+(aq)
(added)
1
Total 10
3
3 (a)(i) The ionic bond in aluminium oxide is strong. 1
(ii) Na3AlF6 1
Total 10
4 (a)(i)
1
.
(ii)
1
(iii)
1
(iv)
1
(b) (i)
1+1
1
(ii) 1+1
[1] [1]
Total 10
4
Section B
164.0
energy
H2 + I2
59.0 53.0
2HI
Progress of reaction
- Labelled axes (no need units) 1
- Correct curves 1
- Energy values marked correctly 1… 8
Total 15
6 (a) (i) - When sodium is added to water, it move vigorously on the surface of water and it 1
burns with a yellow flame.
5
- Hydrogen gas and sodium hydroxide are produced.
2Na + 2H2O → NaOH + H2 1
- Phosphorus does not react with water. 1 …3
(c)
Fractional distillation of an ideal solution
6
Temperature/ oC
100
vapour
liquid
T1
T2
66
0 30 C1 C2 100
% of methanol 1
- The path for the process is shown with arrows 1
- Labelled axes 1
- Correct curves
- The methanol solution would boil at temperature T1, producing vapour of 1
compositon C1
- The vapour with compositon C1 would condense into liquid of the same
composition which will boil at temperature T2 ,producing vapour with 1
composition C2
1
- The boiling and condensation occurs repeatedly
1 …. 7
- The distillate is the component which is more volatile (methanol)
Total 15
Q Answer Mark ∑
7(a)
[ Fe3+ + e Fe2+ Eθ = + 0.77 V ; ½ I2 + e I- Eθ = + 0.54
V]
(i) 2Fe3+ + 2e 2Fe2+ Eθ = + 0.77 V √ 1
- θ
2I I2 + 2e E = - 0.54 V
2I + 2Fe I2 + 2Fe2+ Ecell = + 0.23 V √ √
- 3+ 1+1
Since Ecell is positive, it is a spontaneous reaction / reaction will takes
place. √ 1
(c) (i)
Energy / kJ 1. Atomization of Ca &
ionization of Ca
Ca2+(g) + 2F(g) 2. Atomisation of F and
electron affinity of F
Ca2+(g) + F2(g) 3. formation & lattice
energy of CaF2
Ca2+(g) + 2 F-(g) 4. correct energy circle
+
Ca (g) + F2(g)
Ca(g) + F2(g)
Ca(s) + F2(g)
Ca F2(s)
4 4
(ii)
- 1220 kJ = + 178 kJ + 590 kJ + 1150 kJ + 2(+158 kJ) + 2(-328 kJ)
+L.E. √ 1
L.E. = -1220 – 178 – 590 – 1150 - 2(158) + 656 kJ
= - 2798 kJ mol-1 √ 1 2
15
Q Answer Mark ∑
8
9(a) (i)
I : PCl5/ PCl3/ SOCl2 1
II : Ammonia/NH3 1 2
O O
|| ||
(ii) Amide, H2N- C- CH2CH2-C-NH2 1
1 2
(iii) Reduction 1 1
(iv) Condensation polymerization 1
O O H H
|| || | |
-C-CH2CH2-C – N -CH2CH2CH2CH2-N- OR
H H O O 1
| | || ||
-N - CH2CH2CH2CH2 – N - C-CH2CH2-C –
2
(b) (i) C H O
% by mass 40.0 6.7 53.3
No. of mole 40.0 6.7 53.3
12 1 16
Molar ratio 1 2 1 1
O- H
|
CH3 – C – C – O – H 1
| ||
H O
2-hydroxypropanoic acid 1
3
15
Q Answer Mark ∑
9
10(a) (12.0 x 7 + 1.0 x 6) n = 180 1
n=2
Molecular formula = C14H12 1
2
(b) (i) Structural formula of W
and H 1+1
C=C C=C
H H H
cis trans
Structure of X H
C=C 1
H
Structure of Y
H H
| |
C–C 1
| |
H Br
Structure of Z
H
|
H–C–C 1
| |
H Br
C C
Br Br 1+1
CH2 CH2
H H