t(s) [H2O2] (M)

0 2.32 Cinética química t(s) vs (M)

400 1.72 2.6
800 1.3 2.4

[H2O2] (M)
2.2 f(x) = − 6.155303030303E-11 x³ + 4.90665584415583E-07 x² − 0.00161904761904762 x + 2.31136363636
1200 0.98 R² = 0.999789933611268
2
1600 0.73
1.8
2000 0.54
1.6
2400 0.39
1.4
2800 0.28 1.2
1
0.8
0.6
0.4
0.2
0
0 150 300 450 600 750 900 1050 1200 1350 1500 1650 1800 1950 2100 2250
t (s)

(a) Velocidad inicial

t(s) [H2O2] (M) t(s)
Punto 1 0 2.32 m = ∆y/∆x Punto 1 640
Punto 2 1390 0 1.669E-03 Ms -1
Punto 2 900

(b) Concentración para t=100s

1,669E-03Ms^(-1)=-∆[H_(2 ) O_(2 ) ]/100s →-(1,669E-03Ms^(-1) (100s))=∆[H_2 O_2 ]→

∆[H_2 O_2 ]=[H_2 O_2 ]_f -[H_2 O_2 ]_i=-0,1669M→[H_2 O_2 ]_f = -0,1669M+2,32M → [H_2 O_2
]_f =2,153M

Rapidez instantánea
[H_2 O_2 ]=-6x10^(-11) t^3+5x10^(-7) t^2-0,0016t+2,3114
d[H_2 O_2 ]/dt=-1,8x10^(-10) t^2+1x10^(-6) t-0,0016

r=-(-1,8x 〖 10 〗 ^(-10) t^2+1x 〖 10 〗 ^(-6) t-0,0016)

t(s) [H2O2] (M) [H2O2] (M) r (M/s)

0 2.32 2.32 0.0016 [H2O2] (M
400 1.72 1.72 0.0012288 0.0018

800 1.3 1.3 0.0009152 0.0016

f(x) = 0.00071265553265
r (M/s)

1200 0.98 0.98 0.0006592 0.0014 R² = 0.996660706776011

1600 0.73 0.73 0.0004608 0.0012
2000 0.54 0.54 0.00032 0.001
2400 0.39 0.39 0.0002368 0.0008
2800 0.28 0.28 0.0002112 0.0006
0.0004
0.0002
Constante de proporcionalidad (k)
0
k = 0,0007 Ms-1 0 0.5 1
0.0004
0.0002
0
0 0.5 1
a t(s) vs (M)

00161904761904762 x + 2.31136363636364

Velocidad promedio
Para t = 800s 0.001275 Ms-1
Para t = 1600s 0.00099375 Ms-1

500 1650 1800 1950 2100 2250 2400 2550 2700 2850 3000
(s)

Velocidad instantánea en dos puntos

[H2O2] (M) t(s) [H2O2] (M)
1.44 m=∆y/∆x Punto 1 1498 0.77 m=∆y/∆x
1.2 9.231E-04 Ms -1
Punto 2 1670 0.69 4.651E-04 Ms-1

H_2 O_2 ]→

M → [H_2 O_2

[H2O2] (M) vs r(M/s)

18
16
f(x) = 0.000712655532655817 x − 3.18168374671311E-05
14 R² = 0.996660706776011
12
01
08
06
04
02
0
0 0.5 1 1.5 2 2.5
[H2O2] (M)
04
02
0
0 0.5 1 1.5 2 2.5
[H2O2] (M)