Page 51 - PRE-U STPM CHEMISTRY TERM 1
P. 51
Chemistry Term 1 STPM
(iii) A catalyst decreases the activation energy for the 3
(a) (b) (c) (d)
forward and the reverse reactions by the same
amount. As a result, equilibrium is established Cl – OH – C H COO – SO 3 2–
6
5
in a shorter time.
–
4 HCO + H O H CO + OH –
Energy 3 2 2 3
–
2–
E a = Activation energy HCO + H O CO + H O +
E a 3 2 3 3
without catalyst
E a ' Quick Check 7.3
E a ' = Activation energy
with catalyst 1
Acid K /mol dm –3 pK
a a
Iodoethanoic acid 6.9 10 –4 3.16
Time –4
However, catalyst does not affect the yield or Nitrous acid 7.2 10 3.14
equilibrium constant for the reaction. It also Cynic acid 3.6 10 –4 3.44
does not alter the enthalpy change of reaction. –10
(b) The forward reaction is exothermic. Thus, it is Boric acid 5.8 10 9.23
favoured by low temperature. However, if the – +
temperature is too low, the rate of reaction will be 2 (a) CH COOH + H O CH COO + H O
3
3
2
3
+
–
slow and it takes a longer time for equilibrium to [CH COO ][H ]
3
establish. Thus, a compromise temperature of 450 C (b) K = [CH COOH]
o
a
3
is used where the yield is reasonable and the rate not (c) 1.80 10 mol dm –3
–5
too slow. In order to increase the rate further, finely (d) 4.74
divided iron is added as a catalyst. –6 –3
The forward reaction is accompanied by a decrease in 3 (a) 1.70 10 mol dm
+
the number of moles of gas. Hence, it is favoured by (b) N H + H O N H + OH –
2
2
5
2
4
high pressure. However, if the pressure is too high, (c) 2.60 10 –3
the cost of production will also be high as the pipes 4 (a) HSO + H O SO + H O +
–
2–
3
2
3
3
and storage tanks must be strong enough to withstand [H ][SO ]
+
2–
the high pressure. As a compromise, a pressure of (b) K = 3
–
500 atm is used. a [HSO ]
3
(c) 7.21
Chapter 7 Ionic Equilibria and Quick Check 7.4
Solubility Equilibria 1 (a) H CO + H O H O + HCO –
+
2 3 2 3 3
–
HCO + H O H O + CO 2–
+
Quick Check 7.1 3 2 3 3
[H ][HCO ]
–
+
(b) K = 3
(a) (b) (c) (d) (e) a, 1 [H CO ]
3
2
+
2–
Cu 2+ SO AlCl H + H + [H ][CO ]
3 3 3
K =
–
a, 2 [HCO ]
Quick Check 7.2 –17 3 2 –6
1 (c) 2.06 10 mol dm
+
Acid Base Conjugate Conjugate 2 (a) H PO H + H PO 4 –
3
4
2
base acid
+
–
H PO H + HPO 2–
(a) NH + H O NH H O + 2 4 4
4 2 3 3 2– + 3–
HPO H + PO
(b) H O CN – OH – HCN 4 4
2 [H ][H PO ]
+
–
(c) [Cu(H O) ] 2+ H O [Cu(H O) OH] + H O + (b) K = 2 4
2 6 2 2 5 3 a, 1 [H PO ]
(d) HCOOH HCOOH HCOO – HCOOH + + 3 4 2–
2 [H ][HPO ]
4
K =
(e) H O + C H O – H O C H OH a, 2 –
3 2 5 2 2 5 [H PO ]
2
4
3–
+
(f) H O NH – OH – NH [H ][PO ]
2 2 3 4
K =
a, 3 [HPO ]
2–
4
2 –22 3 –9
(a) (b) (c) (d) (e) (f) (c) 1.99 10 mol dm
C H NH + H CO H SO NH OH + H O + CH CONH +
2 5 3 2 3 2 4 2 2 3 3 3
374
12 Answers.indd 374 3/26/18 4:06 PM

