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A non-natural amino acid has been synthesized. The carboxylic acid has a pk - 3.21, the...
A non-natural amino acid has been synthesized. The carboxylic acid has a pk - 3.21, the protonated amine has a pk = 9.59, and the side chain contains an alcohol which has a pk = 16.09. What is the pl of this amino acid? Your answer should be to the nearest hundredths. a Answer:
A non-natural amino acid has been synthesized. The carboxylic acid has a pk - 3.21, the protonated amine has a pk = 9.59, and the side chain contains an alcohol which has a pk = 16.09. What is the pl of this amino acid? Your answer should be to the nearest hundredths. a Answer: For each compound, indicate if it will or will not produce one of the 20 naturally occuring amino acids if used as the starting material in...
A non-natural amino acid has been synthesized. The carboxylic acid has a pk = 3.04, the protonated amine has a pk, = 9.43, and the side chain contains a pyridine which, when protonated, has a pk, = 5.20. What is the pl of this amino acid? Your answer should be to the nearest hundredths. 00 ton Answer:
1. There are a total of amino acids are called natural amino acids that are found in proteins. These according to the older Greek letter nomenclature system for designating carboxylic acid structures. 2. True/ False The alpha carbon is the carbonyl carbon of the carboxylic acid functional group of the amino acid. 3. Which of the following are functional groups in an amino acid? (choose all that apply) a. amine b. amide c. carbonyl d. carboxylic acid e. alcohol f....
The pK of the side chain of amino acid X in a polypeptide is normally in the range of 9-10 and carries a positive charge when protonated. Suppose you have a soluble globular protein and you find there is an X that has a pK of 6.5. What is the most likely reason for such a large drop in pK? Circle the correct answer. a) X is on the surface of the protein where it ion pairs with the carboxylate...
of alanine has a pk of 9.87. What is the 153, The amino group charge on that amino group at pH 7.0 145. Which amino acid serves as the first amino acid at the hN terminus of a newly synthesized protein? (B) methionine (A) alanine 9.80. The side chain of that amino acid includes (A) an amine group (C) a carboxylic acid group. (D) an alcohol 154. A certain amino acid has a pl (or pH, isoelectric point) (D) threonine...
Consider a 0.203 L solution of the amino acid aspartic acid (0.615 M), which has an alpha carboxylic acid group (pka = 2.10), an alpha amine group (pka = 9.82), and a carboxylic acid group in the side chain (pka = 3.86). If the titration is started at a very low pH, how many liters of 2.15 M NaOH would you need to add to reach the isoelectric point of the amino acid? Give your answer to 3 significant figures...
help with this question Consider a 0.211 L solution of the amino acid aspartic acid (0.631 M), which has an alpha carboxylic acid group (pka = 2.10), an alpha amine group (pka = 9.82), and a carboxylic acid group in the side chain (pka = 3.86). If the titration is started at a very low pH, how many liters of 2.25 M NaOH would you need to add to reach the isoelectric point of the amino acid? Give your answer...
What is the one-letter code for the amino acid that has a side chain that contains a secondary alcohol? T K A E G Correct answer is T What is the one-letter code for the amino acid that has a methyl group as its side chain? E A T G K Correct answer is A
(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,...