P3.1: In the atmosphere, molecular oxygen is photochemically decomposed as follows: 02+hv0(D) + O(3P) The major loss processes for these atoms are: (3.1) O(D)+MO(3P) +M and (3.2) O(3P)+O+MO+M (3.3) with rate constants k and k, respectively and where M is N or 02. and noting (a) By equating the rate of reaction (3.1) to I abs reaction (3.2), write down a kinetic equation for d[O('D)]/dt. (b) Using the result in (a) find an approximate expression for [O('D)] by applying the steady-state hypothesis to O('D). (c) By integration of the rate law in (a) show that

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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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O(1D) is just O*

O(3P) is just oxgen molecule O.

adapted from the textbook atmospheric chemistry: from the surface to the stratosphere (Grant Ritcie)

could you plz provide the solutions for questions A to F

P
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P3.1: In the atmosphere, molecular oxygen is photochemically
decomposed as follows:
O2+ hv→ O(¹D) + O(³P)
O(¹D) + MO(³P) + M
[O(¹D)] =
The major loss processes for these atoms are:
Atmospheric Chemistry 3 Stratospheric Chemistry
and
O(³P) + O₂ + M→ 03 + M
ereader.perlego.com
(3.1)
(3.3)
2
with rate constants kand k, respectively and where M is N₂ or
0₂.
Tabs
ka [M]) (1 - exp(-kg[M]t))
(3.2)
(a) By equating the rate of reaction (3.1) to I and noting
abs
reaction (3.2), write down a kinetic equation for
d[O('D)]/dt.
(b) Using the result in (a) find an approximate expression for
[O(D)] by applying the steady-state hypothesis to O(D).
(c) By integration of the rate law in (a) show that
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Transcribed Image Text:P O iil Q ☎ 8 E 99 {0} 13 of 19 P3.1: In the atmosphere, molecular oxygen is photochemically decomposed as follows: O2+ hv→ O(¹D) + O(³P) O(¹D) + MO(³P) + M [O(¹D)] = The major loss processes for these atoms are: Atmospheric Chemistry 3 Stratospheric Chemistry and O(³P) + O₂ + M→ 03 + M ereader.perlego.com (3.1) (3.3) 2 with rate constants kand k, respectively and where M is N₂ or 0₂. Tabs ka [M]) (1 - exp(-kg[M]t)) (3.2) (a) By equating the rate of reaction (3.1) to I and noting abs reaction (3.2), write down a kinetic equation for d[O('D)]/dt. (b) Using the result in (a) find an approximate expression for [O(D)] by applying the steady-state hypothesis to O(D). (c) By integration of the rate law in (a) show that Q₁ ធ < Previous chapter Next chapter >
P
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[O(¹D)] =
Atmospheric Chemistry 3 Stratospheric Chemistry
||||
ereader.perlego.com
(c) By integration of the rate law in (a) show that
Tabs
ka [M]
(1 exp(-ka [M]t))
assuming constant irradiation is applied after t = 0 and
that no O(¹D) exists prior to this time. Under what
conditions does this expression correspond to the
approximate result derived in (b)?
(d) In the atmosphere at an altitude of ca. 80 km, [M] ≈ 3 ×
-3
14
10 molecules cm and the composite k for N₂ and O₂ is
2
3
-1 -1
3 x 10 cm molecule S . Estimate the minimum
illumination time required for the non-steady-state and
steady-state concentrations to be identical to within 1%. Is
the steady-state hypothesis a good approximation for the
atmospheric behaviour of O(D) where the solar intensity
changes over periods of hours?
(e) Neglecting reaction (3.2), give steady-state and non-steady-
state expressions for [O(P)] in terms of I
Labs, k₁, [M], and
[0₂] assuming the latter concentrations are in excess.
(f) Under atmospheric conditions corresponding to part (d), k,
-33 6
-2 -1
≈ 1.4 x 10 cm molecule s. Is the steady-state
hypothesis a suitable approximation to apply to O(³P) in
-11
15
Q₁
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Transcribed Image Text:P O iil Q මා 8 E 99 {0} 13 of 19 [O(¹D)] = Atmospheric Chemistry 3 Stratospheric Chemistry |||| ereader.perlego.com (c) By integration of the rate law in (a) show that Tabs ka [M] (1 exp(-ka [M]t)) assuming constant irradiation is applied after t = 0 and that no O(¹D) exists prior to this time. Under what conditions does this expression correspond to the approximate result derived in (b)? (d) In the atmosphere at an altitude of ca. 80 km, [M] ≈ 3 × -3 14 10 molecules cm and the composite k for N₂ and O₂ is 2 3 -1 -1 3 x 10 cm molecule S . Estimate the minimum illumination time required for the non-steady-state and steady-state concentrations to be identical to within 1%. Is the steady-state hypothesis a good approximation for the atmospheric behaviour of O(D) where the solar intensity changes over periods of hours? (e) Neglecting reaction (3.2), give steady-state and non-steady- state expressions for [O(P)] in terms of I Labs, k₁, [M], and [0₂] assuming the latter concentrations are in excess. (f) Under atmospheric conditions corresponding to part (d), k, -33 6 -2 -1 ≈ 1.4 x 10 cm molecule s. Is the steady-state hypothesis a suitable approximation to apply to O(³P) in -11 15 Q₁ ធ < Previous chapter Next chapter >
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