Given that pK1 = 3.0 and pK2 = 8.0 for an amino acid X. Total concentration of amino acid X in solution is 10 mM.
Calculate the concentrations of protonated form (P), dipolar form (Z) and de-protonated form (D) of amino acid X at pH 2, and 10.
Given that pK1 = 3.0 and pK2 = 8.0 for an amino acid X. Total concentration...
#1) a) The pK1, pK2, and pKR for the amino acid histidine are 1.8, 9.3, and 6.0, respectively. At pH 4.0 would be charged predominantly as follows: A a-carboxylate 0, a-amino +1, imidazole +1, net charge +2 B a-carboxylate +1, a-amino +1, imidazole −1, net charge +1 C a-carboxylate −1, a-amino +1, imidazole 0, net charge 0 D a-carboxylate +1, a-amino 0, imidazole −1, net charge 0 E a-carboxylate −1, a-amino +1, imidazole +1, net charge +1 b) The pK1,...
The amino acid Tyrosine (H3Tyr) has pK1 = 2.41, pK2 = 8.67, and pK3 = 11.01. (a) What is the principal form of Tyrosine at pH 9.5 and why? (b) What is the second prominent species at pH 6.5 and pH 10.8? *Please show all work! Thank you!!
Which of the following describes the pI of an amino acid? Select one: Oa. the pH at which the amino acid is primarily in the zwitterion form b. the pH at which there are equal concentrations of protonated and neutral forms c, the negative log of the concentration of the ionized amino acid d. the pH of the buffer solution used in electrophoresis that causes the amino acid to migrate to the positive electrode 0 O
(b) The amino acid lysine has the following values of pK : PK1 =2.2, pK2 = 8.9, PKR = 10.5 (the pK, of the amino group in the side chain). At pH 7 it has the structure shown below (6). Draw the structure that you would expect for lysine at pH 9.7, indicating the charges as appropriate. HZN 0 HINA (2 marks) (c) Phenol (C6H5OH) and 2,4,6-trichlorophenol (C6H2C13OH) are both weak acids with pK, values of 9.89 and 6.21, respectively,...
The following questions is based on ionization of carbonic acid. [H2CO3 = H+ + HCO3- K1 = 4.7 X 10-7, pK1 = 6.34 ] [HCO3- = H+ CO3-2 K2 = 4.4 X 10-11, pK2 = 10.36] Calculate the pH ofthe solution form by mixing the following: a)50.0ml of 0.100 M H2CO3 with 50.0ml of 0.050 M NaOH . b)50.0ml of 0.100 M H2CO3 with 50.0ml of 0.150 M NaOH . c)50.0ml of 0.100 M H2CO3 with 50.0ml of 0.100 M...
Alanine (H2NCH(CH3) is a common amino acid that has a basic amino group. A) Write an equilibrium for the reaction of alanine acting as a Bronsted base with a water molecule. (Ka of protonated amino group = 1.349 x 10 -10 B) Calculate the Kb of the amino group C) Calculate the pOH of a 0.025M solution of alanine in water D) Calculate the pH value of a 0.025M solution of alanine in water E) Describe how the equilibrium would...
The sidechain thiol of the amino acid cysteine has a pKa value of 8.37. Ka=4.26E-9 Give the standard free energy change for the sidechain acting as an acid at 30 degrees C. If the pH of the solution is 7.6, what is the [H3O+] in solution? If the pH of the solution is 9.8000000000, what fraction of deprotonated to protonated cysteine sidechains will exist in solution? What is the concentration of protonated cysteine sidechains if the pH of the solution...
(Submit completed assignment via Canvas as a pdf for credit. Show all work.) Dipolar on Draw the structure of L-isoleucine in the zwitterion form, What pH values would you expect this to be the predominant form of this amino acid? 1) 2) If a solution containing isoleucine has a pH of 4 and the concentration of the zwitterion form is 0.02 M, what is the concentration of the fully protonated form? Calculate the isoelectric point of isoleucine (e.g. the pH...
Calculate the concentration of acetate in 20 mM solution of acetic acid at pH 3.0.
Calculate the pH and the concentrations of all species present in 0.11 M ascorbic acid (H2C6H6O6) solution. (Ka1=8.0×10−5), (Ka2=1.6×10−12) Part A: Calculate the pHpH of a 0.11 MM solution of ascorbic acid. Part B: Calculate the concentration of H2C6H6O6 in a 0.11 MM solution of ascorbic acid. Part C: Calculate the concentration of HC6H6O6−HC6H6O6− in a 0.11 MM solution of ascorbic acid. Part D: Calculate the concentration of C6H6O62−C6H6O62− in a 0.11 MM solution of ascorbic acid Part E: Calculate...