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Draw the pentapeptide CANDY with the biologically-preferred stereochemistry and ionization states expected at pH 7
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- The pKa, of the conjugate acid of morpholine is 8.33. (a) Calculate the ratio of morpholine to morpholinium ion in aqueous solution at pH 7.0. (b) At what pH are the concentrations of morpholine and morpholinium ion equal?please explain What percentage of a side-chain sulfhydryl group of cysteine is protonated at pH 7.9?1a) Biotin has a single ionizable group with a pKa of 4.5. If you dissolved biotin in an aqueous solution at pH 7.0, would this ionizable group be protonated or deprotonated? Briefly explain why the molecule would be in that form at pH 7.0.
- The isoelectric point (pl) of phenylalanine is pH 5.5. Draw the structure of the major form of glutamic acid at pH values of (a) 1 (b) 5.5 (c) 11.0.What is the ratio of ionized:unionized amine of glycine (pKa 9.60) in a solution at pH 8.0?Calculate the ratio of ethyl amine (CH3CH2NH2) to the ethyl ammonium ion (CH3CH2NH3+) in a solution with a pH of 11.0. pKa for CH3CH2NH3+ = 10.636.
- i) Draw the D- and L- isomer for tyrosine using Fischer projection ii) Sketch the titration curve for tyrosine. Use the following information : (pKa of α-COOH = 2.20, pKa of α-NH3+ = 9.11, pKa sidechain = 10.07) iii) Draw all the ionic structural formulae for tyrosine and label the region in the figure which they exist at. (You do not have to show the stereochemistry)Hyaluronic acid, a component of connective tissue, is the fluid that lubricates joints. It is a polymer of alternating N-acetyl-d-glucosamine and d-glucuronic acid subunits joined by β-1,3'-glycosidic linkages. Draw a short segment of hyaluronic acid.Draw the structure of fulvic acid chelated with Pb²+ at pH 8.0.
- The pKa values of the carboxylic acid groups of oxaloacetic acid are 2.22 and 3.98.a. Which carboxyl group is the stronger acid?b. The amount of hydrate present in an aqueous solution of oxaloacetic acid depends on the pH of the solution: 95% at pH 0, 81% at pH 1.3, 35% at pH3.1, 13% at pH 4.7, 6% at pH 6.7, and 6% at pH 12.7. Explain this pH dependence.The pKa values of the carboxylic acid groups of oxaloacetic acid are 2.22 and 3.98. a. Which carboxyl group is the stronger acid? b. The amount of hydrate present in an aqueous solution of oxaloacetic acid depends on the pH of the solution: 95% at pH 0, 81% at pH 1.3, 35% at pH 3.1, 13% at pH 4.7, 6% at pH 6.7, and 6% at pH 12.7. Explain this pH dependence.Esterase is an enzyme that catalyzes the hydrolysis of esters. It hydrolyzes esters of L-amino acids more rapidly than esters of d-amino acids. How can this enzyme be used to separate a racemic mixture of amino acids?