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- Predict the pH of 29 mM serine.According to the Henderson–Hasselbalch equation, when the pH of a solution of histidine is 1.85, what is the ratio of the carboxylic acid form of the molecule to its conjugate base (the carboxylate form)? [For practice, either use Marvin Sketch or a piece of paper to draw the acid and conjugate base.] 1 or 4?If the pH of the blood of most animals shifts 0.3 units. above or below. the normal range (7.3-7.5), what is going to happen?
- The pKa of the conjugate acid of guanidine is 13.6, making it one of thestrongest neutral organic bases. Offer an explanation.Define Acid–Base Properties of amino acid ?The amino acid tyrosine has pKa = 2.20 for deprotonation of its carboxylic acid group. What are the relative concentrations of tyrosine and its conjugate base at a pH of (a) 7, (b) 2.2, (c) 1.5?
- Consider the amino acid valine, whose pKavalues are given below. (a) Draw the major form of valine when in a solution of pH = 6.0. (b) Draw the major form of valine when in a solution of pH = 12.0n the laboratory, a general chemistry student measured the pH of a 0.354 M aqueous solution of diethylamine, (C2H5)2NH to be 12.177. Use the information she obtained to determine the Kb for this base. Kb(experiment) =Calculate the pH of the following: - 0.10 M alanine hydrochloride
- A structure of tyrosine is given and I need to draw the structure for neutral solution, pH 2 and pH 12In a typical laboratory set-up, what conditions are necessary in carrying out acid/base hydrolysis of proteinsIf the concentration of an acid in solution is 2.3 times larger than the concentration of its conjugate base, and the pH of the solution is 4.9, what is the pKa of the acid?