- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 1 (463.71 KiB) Viewed 80 times
- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 2 (414.09 KiB) Viewed 80 times
- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 3 (362.63 KiB) Viewed 80 times
- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 4 (454.68 KiB) Viewed 80 times
- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 5 (455.03 KiB) Viewed 80 times
- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 6 (462.85 KiB) Viewed 80 times
- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 7 (457.4 KiB) Viewed 80 times
- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 8 (347.95 KiB) Viewed 80 times
- The Structure Of Anserine At Ph 7 Is Shown Below It Has Three Ionizable Groups The Carboxyl Group Pka1 2 64 Imidazo 9 (535.46 KiB) Viewed 80 times
The structure of anserine at pH 7 is shown below. It has three ionizable groups: the carboxyl group pka1 = 2.64, imidazole nitrogen pKa2 = 7.04, and amino H₂N 20 H₂C NH Complete the paragraphs to describe the titration curve for anserine: Starting at acidic pH, As base is added, After the first deprotonation the molecule will have a As the pH approaches 7, the Finally, as the pH passes Regarding the shape of the graph; charge. and by about pH This
Complete the paragraphs to describe the titration curve for anserine: Starting at acidic pH, As base is added, After the first deprotonation As the pH approaches 7, th Finally, as the pH passes Regarding the shape of the graph; no groups will be protonated, thus the molecule will have a -3 charge all three groups will be protonated, thus the molecule will have a neutral charge all three groups will be protonated, thus the molecule will have a +3 charge all three groups will be protonated, thus the molecule will have a -1 charge all three groups will be protonated, thus the molecule will have a +2 charge no groups will be protonated, thus the molecule will have a -1 charge
a Complete the paragraphs to describe the titration curve for anserine: Starting at acidic pH, As base is added, After the first deprotona the protonated amino group will deprotonate with a midpoint at 7.04 the carboxylic acid group deprotonates with a midpoint of 3.42 As the pH approaches 7 the protonated amino group will deprotonate at around pH 5 Finally, as the pH passe the carboxylic acid group will deprotonate with a midpoint at pH 2.64 Regarding the shape of the graph;
Complete the paragraphs to describe the titration curve for anserine: Starting at acidic pH, 7 As base is added, After the first deprotonation the molecule will have a As the pH approaches 7, the Finally, as the pH passes Regarding the shape of the graph; charge.
H₂C NH he paragraphs to describe the titration curve for anserine: acidic pH, dded, ✓ charge. st deprotonation the molecule will have a pproaches 7, the e pH passes imidazole nitrogen will be 50 % deprotonated leaving the molecule with a -2 charge imidazole nitrogen will deprotonate. After this deprotonation the molecule will have a +1 charge e shape of the graph; imidazole nitrogen will be 50 % deprotonated. After this deprotonation the molecule will be uncharged amino group will deprotonate leaving the molecule with a -1 charge amino group will be 50% deprotonated. After this deprotonation the molecule will have a +2 charge
plete the paragraphs to describe the titration curve for anserine: ing at acidic pH, se is added. the first deprotonation the molecule will have a pH approaches 7, the as the pH passes ing the shape of the gra 9.76, the carboxyl group will be 50 % deprotonated about 7.6, the carboxyl group will be 50 % deprotonated 9.49, the amino group will be 50 % deprotonated about 10, the amino group will be 50 % deprotonated charge.
and by about pH 12.2, the molecule will have no charge 13.5, the molecule will have a -3 charge 9.49, amino group will protonate 14, the carboxyl group will protonate 11.5, the molecule will have a -1 charge
H₂C NH Complete the paragraphs to describe the titration curve for anserine: Starting at acidic pH, As base is added, After the first deprotonation the molecule will have a As the pH approaches 7, the Finally, as the pH passes Regarding the shape of the graph; charge. 1 and by about pH in the region of each pK₂, there is a sharp increase in pH as increments of OH- are added in the region of each pK₂, pH remains relatively unaffected as increments of OH- are add is almost linear as OH- is added throughout the titration
Starting at acidic pH, As base is added, After the first deprotonation the molecule will have a As the pH approaches 7, the Finally, as the pH passes Regarding the shape of the graph; ✓charge. the molecule is a strong acid, which fully dissociates in solution Su the weak base and its conjugate acid are working as a buffer the weak acid and its conjugate base are acting as a buffer