What is the correct structure of histidine at pH 1? The pKa values are 1.8 (carboxylic...
What is the correct structure of histidine at pH 1? The pKa values are 1.8 (carboxylic acid), 9.2 (amine (conjugate acid)), and 6.0 (sidechain, the double bonded N in ring)?
Question 17 (4 points) What is the correct structure of histidine at pH 1? The pKa values are 1.8 (carboxylic acid). 9.2 (amine (conjugate acid)), and 6.0 (sidechain, the double bonded N in ring)? OH NH H2 СНС NH С NH H2 CHC 뿔 NH OH H2 NH CH-C NH2 ON 0 NH 42 CH-C NH3
Question 15 (4 points) What is the correct structure of histidine at pH 1? The pKa values are 1.8 (carboxylic acid), 9.2 (amine (conjugate acid)), and 6.0 (sidechain, the double bonded N in ring)? OH OC H2 NH CH NH, NH CH NH o NH CHC NH ON OH С NH H2 CH-C NH2 Question 16 (4 points) Which one is the major product of the following reaction sequence? NH2 1. excess CH31 2. Ag,0,H,O heat M my
What is the correct structure of cysteine at pH 137 The pKa values are 1.7 (carboxylic acid), 10.8 (amine (conjugate acid)), and 8.3 (sidechain, thiol). ΝΗ, * _dp OH ΝΗ, HS H2 -CÁCH NH2 CH es O Arrange the indicated protons by acidity, most acidic first: So ho į III IV OI>I> III > IV 01>II> III > IV 01> IV> III > II >I> IV > III Friedel-Crafts alkylation reactions cannot be performed on aniline because: The amino group...
(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...
2. (10 points) The structure for the amino acid histidine is shown below (at pH 1). Write the chemical equations for the ionic dissociations of histidine (as the pH increases) Determine the isoelectric point for histidine and indicate the structure present at the isoelectric point. The pka values for histidine are 1.82 (-CO2H). 9.17 (NH3'), and 6.00 (R group). OOH "HaN NH "INP
Inspect the compounds below. The brackets contain the pKa values for the acids. NH (pKa =9.2); CH:OH (pKa = 16); CH SO;H (pKa =-6.5); CH3COOH (pKa = 4.7) Of the compounds given above, which is the conjugate base of the weakest acid? (a) NH (b) CHO (c) CH SO (d) CH3COO (e) The answer cannot be determined from the information provided.
1) The pKa for the imidazole group in histidine in Papain's catalytic centers is 8.3. What is the ratio of protonated and deprotonated His-R groups at pH 8.2? a) 5 NH+ / 4 N: b) 1 NH2+ / 1 NH c) 4 N: / 5 NH+ d) 1 NH / 1 NH2+ 2) What is the ratio of protonated vs deprotonated Cysteine sulfhydryl groups in the catalytic center of papain, pKa 3.4, at optimal pH of 6.2? a) 1 S-...
1,2,and 3 please!! Post-Lab Questions 1. The pKa value for the carboxylic structure of acetic acid at (a) pH- 1, (b) pH-7, and (c) p-13 acid group in acetic acid is 4.75. Write the predominant 2. Fill in the following table to show the theoretical results for the titration of 1.0 L of 0.20 M acetic acid by adding the designated amount of solid (no volume change) potassium hydroxide, KOH. Show a sample calculation of your work below. pH IH'T...
What kinds of interactions are NOT part of tertiary protein structure? 3 . A) salt bridges In a hydrolysis reaction, B) hydrophilic interactions A. an acid reacts with an alcohol. C) disulfide bonds E. an este reacts with NaOH. C. anester reacts with H.O. D) peptide bonds D. an acid neutralizes a base. E) hydrophobic interactions E. water is added to markene. . All amino acids have chiral Carbon atoms except a. Val 6. Lys C. ASP d. Ala e....