Using the pKa values given in the Table, where the acidic proton is in bold, indicate which structure will predominate in an aqueous solution at the given pH values. Compound pKa Glycine α-carboxylic acid proton (+NH3CH2COOH) 2.3 Glycine ammonium proton (+N(H)3CH2COO−) 9.6 Oxalic acid first proton (HOOCCOOH) 1.25 Oxalic acid second proton (−OOCCOOH) 4.15 Drag the appropriate equation to their respective bins.
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Using the pKa values given in the Table, where the acidic proton is in bold, indicate...
For
each of the following reactions, use the pKa values given in the
Table to predict whether reactants or products are favored at
equilibrium.
For each of the following reactions, use the pKa values given in the Table to predict whether reactants or products are favored at equilibrium Compound Hydronium ion (H30*) Dichloroacetic acid (C2H202Cl2) Dihydrogen sulfide (H2S) Phenol (C6H5OH) Piperidinium ion (C5H12N*) Water (H20) pKa 1.7 1.35 7.0 10.0 11.2 15.7 Drag the appropriate items to their respective bins....
For the following problems, use the pK,' values given in Table 2-3 2-6 How many mL of 0.1 M sodium acetate should be added to 100 mL of 0.1M acetic acid to make a buffer of pH 5.1? What is the molarity of the resulting buffer with respect to acetate (acetate + acetic acid)? Table 2-2 The pKa Values of Common Buffers COMPOUND DK Oxalic 1.27 Histidine 1.82 Phosphoric 2.15 Glycine 2.35 Citric 3.13 Citric 4.76 4.76 Acetic Histidine 6.04...
Using the pKa values given in the table on the right,
determine the charge of the side group of the following amino acids
at the pH specified. Consider the side group only (not including
the charges at the C–terminal or N– terminal).
2. Using the pka values given in the table on the right, determine the charge of the side group of the following amino acids at the pH specified. Consider the side group only (not including the charges at...
Exercise 2 Separation of a Mixture Based on Acid-Base Properties One purpose of this exercise is to learn how to use a separatory funnel to extract a single component away from other compounds in solution. To do so, we will apply the principles of solubility and acid-base behavior you’re seeing in class. One of the compounds is neutral in the acid-base sense. It has no ability to either donate or accept a proton from an aqueous solution, and will remain...