#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, pK2, and pKR for the amino acid arginine are 1.8, 9.0, and 12.5, respectively. At pH 7.0 arginine would be charged predominantly as follows:
A |
a-carboxylate +1, a-amino 0, guanidino -1, net charge 0 |
B |
a-carboxylate 0, a-amino 0, guanidino +1, net charge +1 |
C |
a-carboxylate −1, a-amino +1, guanidino +1, net charge +1 |
D |
a-carboxylate −1, a-amino 0, guanidino +1, net charge 0 |
E |
a-carboxylate +1, a-amino −1, guanidino −1, net charge −1 |
c) The pK1, pK2, and pKR for the amino acid aspartic acid are 2.0, 9.9, and 3.9, respectively. At pH 7.0, aspartic acid would be charged predominantly as follows:
A |
a-carboxylate +1, a-amino +1, b-carboxylate +1, net charge +3 |
B |
a-carboxylate 0, a-amino +1, b-carboxylate 0, net charge +1 |
C |
a-carboxylate 0, a-amino −1, b-carboxylate 0, net charge −1 |
D |
a-carboxylate +1, a-amino −1, b-carboxylate +1, net charge +1 |
E |
a-carboxylate −1, a-amino +1, b-carboxylate −1, net charge −1 |
#1) a) The pK1, pK2, and pKR for the amino acid histidine are 1.8, 9.3, and...
(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 amino acid Prolinehas a pk1 of 1.99, pk2 of 10.60. The amino acid Serine has pk1 of 2.21 and a of pk2 of 9.15. If these two amino acids bind together by peptide bond creating the peptide sequence Pro-Ser . What will be the overall charge of this peptide at the physiological pH of 7?
(1) The following diagram represents a titration curve of histidine as pH increases; pKa = 1.82 represents the terminal carboxylic acid group. pK, represents the terminal amino group: 6.0 represents the R-group, and pK, E 9.17 7.59 pH 182 3.0 20 10 H (equivalents) At what point on the diagram is histidine predominantly present as the following species? COO A, at pH < 1.82 B. between pH 1.82 and pH 6.0 C) between pH 6.0 and pH 9.17 D. at...
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!!
#1) For the following pentapeptide (Where pH =1): a) What would the net charge be for the following pH? pH 0 = pH 3 = pH 5 = pH 7 = pH 10 = pH 13 = b) Calculate the pl of the pentapeptide. (Cysteine: pK1 = 1.96, pK2 = 10.128) ( Glutamine: pK1 = 2.17 , pK2 = 9.13) (Arginine: pK1 = 2.17. pK2 = 9.04) (Leucine: pK1 = 2.36 , pK2 = 9.60) c) If you were to...
please help with these 4 questions and explain why you chose what you did. thanks and I'll give thumbs up. 11. A particular amino acid without an ionizable R-group would have a pl of is 3.1 and pK2 is 8.9 ; if its pK1 2.9 a. b. 5.8 6 C. d. 12 12. A certain amino acid with an ionizable side chain has a pK1 of 2.4, a pK2 of 8.9, and a pKR of 6.5. If the amino acid...
6. At neutral pH, which of the following amino acids has a net positive charge, which has a net negative charge, and which is neutral? (Hint: Draw the various charged forms of each amino acid before deciding.) a) Aspartic acid b) Histidine c) Valine 7. Which of the following forms of aspartic acid would you expect to predominate at low pH, neutral pH, and high pH? a) 10_char Line HOC-CH-CH-CO- +NH, b) ._ança do OC-CH-CH-CO- NH2 HOC-CH.CH +NH
A 1000 mL aliquot of .1 M diprotic acid H2A (pK1=4; pK2=8) was titrated with 1 M NaOH. find pH values at Vb: 0, 3, 8, 10, 13, 19, 20, 22.
) You have a mixture of serine, aspartic acid, and histidine. A) Find a pH value that would separateApply the sample here. the three amino acids from each other B) Draw the structure of serine, aspartic acid, and histidine at the pH chosen in part A. C) Draw how they would move in an electric field at the pH you have chosern. Apply the sample mixture here
please answer part (ii) (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...