The decomposition of salicylic acid to phenol and carbon dioxide was carried out at 200.0°C, a temperature at which the reactant and products are all gaseous. A 0.300 g sample of salicylic acid was introduced into a 50.0 mL reaction vessel, and equilibrium was established. The equilibrium mixture was rapidly cooled to condense salicylic acid and phenol as solids; the CO 2 (g) was collected over mercury and its volume was measured at 20.0 °C and 730 mmHg. In two identical experiment, the volumes of CO 2 (g) obtained were 48.2 and 48.5 mL, respectively. Calculate K e for this reaction, for pressure in atmospheres.
The decomposition of salicylic acid to phenol and carbon dioxide was carried out at 200.0°C, a temperature at which the reactant and products are all gaseous. A 0.300 g sample of salicylic acid was introduced into a 50.0 mL reaction vessel, and equilibrium was established. The equilibrium mixture was rapidly cooled to condense salicylic acid and phenol as solids; the CO 2 (g) was collected over mercury and its volume was measured at 20.0 °C and 730 mmHg. In two identical experiment, the volumes of CO 2 (g) obtained were 48.2 and 48.5 mL, respectively. Calculate K e for this reaction, for pressure in atmospheres.
The decomposition of salicylic acid to phenol and carbon dioxide was carried out at 200.0°C, a temperature at which the reactant and products are all gaseous. A 0.300 g sample of salicylic acid was introduced into a 50.0 mL reaction vessel, and equilibrium was established. The equilibrium mixture was rapidly cooled to condense salicylic acid and phenol as solids; the
CO
2
(g) was collected over mercury and its volume was measured at 20.0 °C and 730 mmHg. In two identical experiment, the volumes of
CO
2
(g) obtained were 48.2 and 48.5 mL, respectively. Calculate
K
e
for this reaction, for pressure in atmospheres.
Please help me figure out what the slope is and how to calculate the half life Using the data provided.
Curved arrows are used to illustrate the flow of electrons. Follow
the curved arrows and draw the structure of the missing
reactants, intermediates, or products in the following mechanism.
Include all lone pairs. Ignore stereochemistry. Ignore inorganic
byproducts.
H
Br2 (1 equiv)
H-
Select to Draw
Starting Alkene
Draw Major
Product
I
I
H2O
四:
⑦..
Q
Draw Major
Charged
Intermediate
I
NH (aq)+CNO (aq) → CO(NH2)2(s)
Experiment
[NH4] (M) [CNO] (M) Initial rate (M/s)
1
0.014
0.02
0.002
23
0.028
0.02
0.008
0.014
0.01
0.001
Calculate the rate contant for this reaction using the data provided in the table.
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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