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Problem- A weak acid (HA) has a pKa of 4.919. If a solution of this acid has a pH of 4.762, what percentage of the acid is not ionized? (Assume all H in solution came from the ionization of HA.)
I just need a general explanation of it please- Thanks!
A buffer containing 0.25 M NH3 (Kb = 1.8 x 10-5) and 0.40 M NH4Cl is prepared. a. What is the pH of this buffer solution. b. What is the pH of the solution after 25.00 mL of 1.00 M HCl is added to 975.0 mL of buffer
Trans-1,4-di-tert-butylcyclohexane exists in a normal chair conformation. Cis-1,4-di-tertbutylcyclohexane, however, adopts a twist-boat conformation. Draw both isomers, and explain why the cis isomer is more stable in a twist-boat conformation.
An environmental chemist obtained a 200 mL sample of lake water believed to be cntaminated with a single monoprotic strong acid.
Strong, non-charged bases are useful in base-catalyzed reactions. Many non-charged nitrogen bases are commonly used in various reactions. Perhaps the strongest non-charged base is shown below
If you wanted to prepare a solution of CO in water at 25 in which the CO concentration was 2.1 mM , what pressure of CO would you need to use
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Using a sample of 350. mL air is collected at 35 Celsius has a pressure of 550. torr. if it is allowed to expand to 425 mL at 57 Celsius then What pressure will the air exert?
How many grams of are CaH2 needed to generate 147L of H2 gas if the pressure of H2 is 827 torr at 20 C?
a 0.21 m3 drum contains 100 l of a mixture of several degreasing solvents in water. the concentration of
Dry air contains 20.94% oxygen by lolume. the solubility of oxygen in water at 25 degrees celsius is 0.041 grams per liter of water. how many liters of water would dissolve the oxygen in one liter of dry air ar 25 degrees celcius and 1.00 atm
calculate the wavelength in nm of an electron traveling at 75% the speed of light. (mass of the electron = 5.4858 x 10^-4 amu)
Explain the use of beta-alanine? Is it used as a H+ source, or something else? Why can malonic acid be reacted in V-D modification, while only its ester can be reacted in standard Knoevenagel condensation conditions?
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