The eouillibrium constant Kc for The reactiun is 7.00 y lo-5 @ 673K. -NH3 (6)+ HI() Calcolae the eaillibrim Cancentratsan of HI when •506 moles of NHy](S) are infroduced mto 1.0L VeSsel @ 673 K.
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- The pseudofirst-order rate constant for the decomposition of urea, CO(NH2)(aq) + 2 H2O(I)→ 2 NH4+(aq) + CO32-(aq). is 1.2 x 10-7 s- 1 at 60 °C and 4.6 x 10-7 s-1 at 70 oc. Estimate (a) the activation Gibbs energy and (b) the entropy of activa tion of the reaction.Potassium dichromate has several industrial applications. To determine the purity of the salt that will be used in different industrial processes, a sample mass equal to 2.660 g was dissolved and quantitatively transferred to a 500.00 mL flask. An aliquot of 25.00 mL of this solution was treated with excess KI and the released iodine was titrated with 0.1000 mol L-1 sodium thiosulfate, spending 27.00 mL. Calculate the purity of the analyzed salt. Data:K = 39.10 O = 16.00 Cr = 52.00 I = 126.9 S = 32.07Calculate the solubility of BaSO4 solid in 0.0167 M Ba(NO3)2 solution, taking into account its activity.(Ksp 1.1x10-10 for BaSO4; activity coefficients for Ba++ and SO42- ions are 0.46 and 0.44, respectively)
- Assume no acid-base catalysis occurs and the following data: Under biological conditions (310 K) 1. dGb = -20.00 kJ/mol. 2. The dG of E +S binding to ES (dGs) is -3.00 kJ/mol. 3. dGd mismatch of energy in ES = +2.00 kJ/mol. What is the catalytic power (kcat/k_uncat) at 360 K? Use 1 decimal place.Hey, The issue I am having here is calculating the partial pressure, if I use P=(n/V)*R*T then I get the partial pressure of H2 as 23.2 but according to the teacher it should be 11.585 so instead of just calculating the the total moles of H2 in the reaction should n be a molar fraction?For the reaction A + B <=> AB, kassoc = 2.0 sec-1 M-1 and kdissoc = 0.5 sec-1. This means that Kassoc is equal to ____ M-1. (Enter your answer to the nearest 0.1; do not include units)
- In Heat of solution from Solubility experiment: the slope of plot of Ln Sversus 1/T (K) = - 534 and the intercept = 2.964, calculate the solubility SThe student then determined ΔH neutralization for the reaction of sodium hydroxide and acetic acid, using the procedure described in this module. The student added 100.0 mL of 0.8500M NaOH to 100.0 mL of 0.8404M acetic acid. Prior to and following the mixing of the acid and base solutions, the following temperature-time data were collected. g) Identify the limiting reagent and briefly explain why it is limiting. h) Find ΔH neutralization for the reaction.Using the kinetic data pictured, estimate Vmax and Km for the catalysis of Substrate 1 by the following enzyme (using the correct units).
- For the reduction 2FeCl3 + SnCl2 =====➔ 2 FeCl2 + SnCl4 in aqueous solution the following data were obtained at 25oC t(min) 1 3 7 11 40 Y 0.01434 0.02664 0.03612 0.04102 0.05058 Where y is the amount of FeCl3 reacted in moles per liter. The initial concentrations of SnCl3 and FeCl3 were respectively, 0.03125, 0.0625 moles/L. a.)Show that the reaction is third order (derive the rate law), and b.) calculate the average specific rate constant.Suppose the concentration of a solute decays linearly along the length of a container according to c(x) = c0 - αc0x, where c0 is the concentration at x = 0. Calculate the thermodynamic force on the solute at 25 °C and at x = 10 cm and 20 cm given that the concentration falls to 1/2c0 when x = 10 cm. Hint: Start by finding the value of α.Hexanoic acid was added to an immiscible biphasic solvent sysem, water and CCl4 at 20.0OC and the equilibrium concentrations of hexanoic acid were determined to be 3.66 g/L in H2O and 67.0 g/L in CCl4. Caluclate the distrubution coeffiecent (D1) of hexanoic acid in CCl4 with respect to water.