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41. (a) mol CO2 = v V = 36.4 L 22.4 L/mol = 1.625 mol (1 Mark)
Molecules CO2 = mol x NA = 1.625 mol x 6.02x1023 molecules/mol = 9.78x1023 molecules CO2 41. (b) Assume 100g sample = 60.00g 12.01 g/mol = 4.9958 mol = 4.485g 1.01 g/mol = 4.4406 mol = 35.52g 16.00 g/mol = 2.22 mol (1.5 Mark) (1 Mark)
41. (c) mol K2Cr2O7 = c x v = 0.150 mol/L x 0.250 L = 0.0375 mol (1 Mark)
41. (d) Many acceptable answers: - inaccurate weighing of solute - inaccurate addition of water (meniscus) - contaminated/wet glassware or equipment - any other acceptable answer
= 0.0829 mol/L
(1 Mark)
0.03059 mol Zn x
= 0.0611 mol Ag
(0.5 Mark)
= 0.0200 mol Ag
(0.5 Mark)
41. (g) A CHCl3 Polar, thus soluble. No conductivity because molecular. B AlCl3 High solubility (solubility table). Thus, high conductivity. C PbCl2 Low solubility (solubility table). Thus low conductivity. NOTE: 0.5 Mark for identifying each substance. 0.5 Mark for each explanation.
42. (a)
Lewis Diagram
(1 Mark)
S
VSEPR Shape Diagram
F
(1 Mark)
V-Shaped or Bent
42. (b)
(1 Mark)
(0.5 Mark)
42. (c) Fluorine < Ammonia < Sodium chloride < Silicon dioxide (1 Mark for Order) LDF LDF D-D H-Bonding (0.5 Marks for each substance justification) Ionic Network covalent
42. (d)
OH H3C
Alcohol LDF (same) Polar (D-D forces) H-Bonds
O H3C
Ether - LDF (same) - Polar (D-D forces)
CH2
CH3
Alcohol will have higher boiling point because of greater intermolecular forces (HBonds) (1 Mark For each diagram) (0.5 Mark for identifying forces in each compound) (1 Mark for conclusion)
HC
CH2
CH3
1-butyne 2-butyne
H3C
CH3
HC
CH
cyclobutene
H2C CH2
CH2
1-methylcyclopropene
HC C CH3
CH3
CH
3-methylcyclopropene
HC
CH
43. (b)
IUPAC Name
Structural Diagram
Hexanoic acid
H3C CH2 CH2 CH2 CH2
O C OH
1,4-difluorobenzene
F
NH2
Ethanamine
H3C CH2
Compound A
Isomer 1
Isomer 2
OH
+ H2O(l)
Compound B
+ HC
3
CH
CH3
+
O H3C C OH
Compound C
+ H2O(l)
(1 Mark for each structure) (All types of diagrams accepted)