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Question 1 (10pts): The amino acid leucine (shown at right) has a...
Question 1 (10pts): The amino acid leucine (shown at right) has a Pkal = 2.36 and Pka2 = 9.60. A) Draw the chemical...
Question 1 (10pts): The amino acid leucine (shown at right) has a Pkal = 2.36 and Pka2 = 9.60. A) Draw the chemical form of leucine as a positive ion, as a negative ion, and as a zwitterion. B) Calculate the isoelectric point of leucine. OH NH2
1. The pKa's of the amino acid methionine are 2.28 and 9.21. The zwitterion of methionine...
1. The pKa's of the amino acid methionine are 2.28 and 9.21. The zwitterion of methionine is given below (1). S Н,с NH3 (a) Explain why structure (I) is an intermediate ion. Write balanced chemical reactions to support your reasoning (b) Draw the conjugate acid AND conjugate base form of the amino acid shown above (c) A 15-mL aliquot solution consisted 0.25M of the zwitterion of methionine and 0.30M of its conjugate acid was titrated with 0.15M NaOH, calculate the...
1. The pKa's of the amino acid methionine are 2.28 and 9.21. The zwitterion of methionine is given below (I) S H3C...
1. The pKa's of the amino acid methionine are 2.28 and 9.21. The zwitterion of methionine is given below (I) S H3C O NH3 (a) Explain why structure (I) is an intermediate ion. Write balanced chemical reactions to support your reasoning. (b) Draw the conjugate acid AND conjugate base form of the amino acid shown above (c) A 15-mL aliquot solution consisted 0.25M of the zwitterion of methionine and 0.30M of its conjugate acid was titrated with 0.15M N2OH, calculate...
#1) For the following pentapeptide (Where pH =1): a) What would the net charge be for...
#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...
(Submit completed assignment via Canvas as a pdf for credit. Show all work.) Dipolar on Draw...
(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...
please answer part (ii) (b) The amino acid lysine has the following values of pK :...
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...
Which amino acid has a net charge of “+ 0.09” at pH 7? Show all calculations....
Which amino acid has a net charge of “+ 0.09” at pH 7? Show all calculations. Draw the structure of the amino acid that would predominate at this pH. (The answer should be Histindine; draw the structure of histidine. Calculate the net charge using a H-H equation. Please walk through every single step as if I was five years old I am very confused).
Please show all work and steps! 13.3 Electric Field - Discrete and Continuous Distributions 2A 2c0...
Please show all work and steps!
13.3 Electric Field - Discrete and Continuous Distributions 2A 2c0 Separately, draw the electric field lines produced by a positive point charge +g: a negative point charge, +2g i q; a charge 2. Draw a constant electric field arrows to the right.) Ignore the electric fields generated by the charges themselves. (a) Place a positive charge q in it. Draw the force vector on this charge. (b) Also, now, place a negative charge q...
5. D-sorbital is found in 'sugar-free' chewing gum. It is formed by reducing D-glucose with NaBH Draw the structure of D-sorbital. s. (4 pts) Classify the following amino acid as polar, n...
5. D-sorbital is found in 'sugar-free' chewing gum. It is formed by reducing D-glucose with NaBH Draw the structure of D-sorbital. s. (4 pts) Classify the following amino acid as polar, non- polar, acidic, or basic: 6 (4 pts) The amino acid threonine (thr) has two chiral carbons. Draw a Fischer projection of the 2S,3S configuration of threonine. キ 7.(11 pts) Draw the tripeptide lys-asp-ser at physiological pH 8. (8 pts) The pK, values for aspartic acid are 2.10, 9.82...
please show work and explain I have attached a titration of a mock amino acid with...
please show work and explain
I have attached a titration of a mock amino acid with OH-. I have labeled the different charge states of the amino acid as I, II, III, IV. I have labeled different points on the titration curve as A, B, ....G. I want you to tell me which form(s) of the species I, II, III or IV predominates (is present at greatest concentration) at each of the lettered points on the curve. I would also...
Question 1 (10pts): The amino acid leucine (shown at right) has a Pkal = 2.36 and Pka2 = 9.60. A) Draw the chemical form of leucine as a positive ion, as a negative ion, and as a zwitterion. B) Calculate the isoelectric point of leucine. OH NH2
1. The pKa's of the amino acid methionine are 2.28 and 9.21. The zwitterion of methionine is given below (1). S Н,с NH3 (a) Explain why structure (I) is an intermediate ion. Write balanced chemical reactions to support your reasoning (b) Draw the conjugate acid AND conjugate base form of the amino acid shown above (c) A 15-mL aliquot solution consisted 0.25M of the zwitterion of methionine and 0.30M of its conjugate acid was titrated with 0.15M NaOH, calculate the...
1. The pKa's of the amino acid methionine are 2.28 and 9.21. The zwitterion of methionine is given below (I) S H3C O NH3 (a) Explain why structure (I) is an intermediate ion. Write balanced chemical reactions to support your reasoning. (b) Draw the conjugate acid AND conjugate base form of the amino acid shown above (c) A 15-mL aliquot solution consisted 0.25M of the zwitterion of methionine and 0.30M of its conjugate acid was titrated with 0.15M N2OH, calculate...
#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...
(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...
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...
Please show all work and steps!
13.3 Electric Field - Discrete and Continuous Distributions 2A 2c0 Separately, draw the electric field lines produced by a positive point charge +g: a negative point charge, +2g i q; a charge 2. Draw a constant electric field arrows to the right.) Ignore the electric fields generated by the charges themselves. (a) Place a positive charge q in it. Draw the force vector on this charge. (b) Also, now, place a negative charge q...
5. D-sorbital is found in 'sugar-free' chewing gum. It is formed by reducing D-glucose with NaBH Draw the structure of D-sorbital. s. (4 pts) Classify the following amino acid as polar, non- polar, acidic, or basic: 6 (4 pts) The amino acid threonine (thr) has two chiral carbons. Draw a Fischer projection of the 2S,3S configuration of threonine. キ 7.(11 pts) Draw the tripeptide lys-asp-ser at physiological pH 8. (8 pts) The pK, values for aspartic acid are 2.10, 9.82...
please show work and explain
I have attached a titration of a mock amino acid with OH-. I have labeled the different charge states of the amino acid as I, II, III, IV. I have labeled different points on the titration curve as A, B, ....G. I want you to tell me which form(s) of the species I, II, III or IV predominates (is present at greatest concentration) at each of the lettered points on the curve. I would also...
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