To study the following reaction at 20 °C , NO ( g ) + NO 2 ( g ) + H 2 O ( g ) ⇌ 2HNO 2 ( g ) a mixture of NO ( g ) , NO 2 ( g ) , and H 2 O ( g ) was prepared in a 10.0 L glass bulb. For NO, NO 2 , and HNO 2 , the initial concentrations were as follows: [ NO ] = [ NO 2 ] = 2 .59 × 10 -3 M and [ HNO 2 ] = 0 M . The initial partial pressure of H 2 O ( g ) was 17.5 torr. When equilibrium was reached, the HNO 2 concentration was 4.0 × 10 − 4 M . Calculate the equilibrium constant, K c for this reaction.
To study the following reaction at 20 °C , NO ( g ) + NO 2 ( g ) + H 2 O ( g ) ⇌ 2HNO 2 ( g ) a mixture of NO ( g ) , NO 2 ( g ) , and H 2 O ( g ) was prepared in a 10.0 L glass bulb. For NO, NO 2 , and HNO 2 , the initial concentrations were as follows: [ NO ] = [ NO 2 ] = 2 .59 × 10 -3 M and [ HNO 2 ] = 0 M . The initial partial pressure of H 2 O ( g ) was 17.5 torr. When equilibrium was reached, the HNO 2 concentration was 4.0 × 10 − 4 M . Calculate the equilibrium constant, K c for this reaction.
NO
(
g
)
+ NO
2
(
g
)
+ H
2
O
(
g
)
⇌
2HNO
2
(
g
)
a mixture of
NO
(
g
)
, NO
2
(
g
)
, and H
2
O
(
g
)
was prepared in a 10.0 L glass bulb. For
NO, NO
2
, and HNO
2
, the initial concentrations were as follows:
[
NO
]
=
[
NO
2
]
= 2
.59 × 10
-3
M
and
[
HNO
2
]
= 0
M
. The initial partial pressure of
H
2
O
(
g
)
was 17.5 torr. When equilibrium was reached, the
HNO
2
concentration was
4.0
×
10
−
4
M
. Calculate the equilibrium constant,
K
c
for this reaction.
Kumada Coupling:
1. m-Diisobutylbenzene below could hypothetically be synthesized by Friedel-Crafts reaction. Write out the reaction with a
mechanism and give two reasons why you would NOT get the desired product.
Draw the reaction (NOT a mechanism) for a Kumada coupling to produce the molecule above from m-dichlorobenzene.
Calculate the theoretical yield for the reaction in question 2 using 1.5 g of p-dichlorobenzene and 3.0 mL isobutyl bromide.
What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Wintergreen from Aspirin:
1. In isolating the salicylic acid, why is it important to press out as much of the water as possible?
2. Write the mechanism of the esterification reaction you did.
3.
What characteristic absorption band changes would you expect in the IR spectrum on going from aspirin to salicyclic acid and
then to methyl salicylate as you did in the experiment today? Give approximate wavenumbers associated with each functional
group change.
What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Synthesis of ZybanⓇ:
1. Write a mechanism for the bromination of m-chloropropiophenone.
Br₂
CH2Cl2
Cl
Br
2. Give the expected m/z (to a round number) for the molecular ion from the product above (including isotopic peaks).
3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell