help with this question Consider a 0.211 L solution of the amino acid aspartic acid (0.631...
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...
1A solution of 0.235 M aspartic acid, the charge neutral form of the amino acid, is titrated with 0.118 M NaOH . The p K a values for aspartic acid are 1.990 , 3.900 , and 10.002 , corresponding to the α-carboxylic acid group, the β-carboxylic acid group, and the amino group, respectively. Calculate the pH at the first equivalence point of this titration.
At a pH of 4: Amino acid 1 OH Amino acid 2 NH OH HN NH, OH pka Amino Amino Acid 1 Acid 2 9.82 9.18 Amino terminus Carboxy terminus 2.1 1.77 Side chain 3.86 6.1 O (Answer B) the R group (side chain) on amino acid 1 will be deprotonated A and B (Answer A) the amino terminus on amino acid OH HN OH pka Amino Acid 1 Amino Acid 2 Amino terminus 9.82 9.18 Carboxy terminus 2.1 1.77...
Incorrect Question 16 0/1 pts This amino acid is +H3N—CH-0-0 CH2 CEO neutral aspartic acid. aspartic acid at its isoelectric point. aspartic acid at a pH that is lower than the isoelectric point. aspartic acid at a pH that is higher than the isoelectric point. Reconsider your answer! Since the nitrogen atom has a positive charge and both carboxylic acid groups have lost a hydrogen atom, this amino acid must be at its isoelectric point.
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...
Question 2 1 pts Amino acids are classified by their Rgroup (side chain) carboxylic acid group peptide bond alpha carbon amine 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...
i have no clue what amino acid this unknown is . maybe serine ?? pleade help! i also need to locate the eq points it can be from 1-3 points but atleasy 2 , the pka2 location , and the expermental molecular weight value. if you can label it on one of the graphs ( they are the same) the chocies are below ( it most likely will not be glycine ) . other data: unknown weight obtained was =...
2. The structure of the solid phase Wang resin linker and the first amino acid that we will use in this lab is shown below Fmoc first amino acid linker a) (1 pt) If the resin has 0.72 mmol/g of this linker on the surface of the beads, and you use 300 mg of resin for the reaction, how many mmol of linker do you have? b) (3 pts) All peptides will use alanine at the C-tenminus (position 1), Fmoc-L-valine...
Understand alpha helices and beta pleated sheets Question Every helical turn in an a-helix has 3.6 amino acid residues. Then, hydrogen bonds are formed between the oxygen atom in amino acid along the the carbonyl group in the first amino acid and the hydrogen atom in the amine group of the chain. Select the correct answer below: third second fourth fifth FEEDBACK MORE INSTRUCTION SUBMIT Content attribution