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0.693
3. t1/2 =
k
0.693
= −14
= 1.26 × 1013 s
5.5 ×10 sec -1
4. 0.011 55 min-1
2.303 [ R ]o
5. t= log
k [ R]
2.303 2 × 10−3
= log
3 × 10−2 min -1 5 × 10−4
2.303
= log 4 (log 4 = 0.6021)
3 × 10−2
= 46.22 min.
6. Arrhenius equation
K = A e –Ea/RT
Where K = rate constant , T = absolute temperature
Ea = Activation energy, R = gas constant.
7. K = A e-Ea/RT
When Ea = 0
K = A e -0/RT
8. T1 = 295K T2 = 305K
TT k
Ea = 2.303 R 2 1 log 2
T2 − T1 k1
K2 = 2k1
305 × 295 2k
Ea = 2.303 ×8.314 × log 1
305 − 295 k1
= 2.303 × 8.314 × 8997.5K log 2
= 51855.2 J/mol (log2 = 0.3010)
9. 22.0 KJ/mol.
10.