Looking at the following graph, determine the pKb of the compound 14.0 12.0 10.0- 8.0 6.0...
14.0 2.0 10.0 equivalence point pH=7.0 8.0 6.0 4.0 2.0 0.0 0.0 20.0 40.0 6o.0 80.0 Volume of NaOH added (ml) Figure 16.15. A strong acid-base titration curve. 50.0 mL of 0.100 M titrated with 0.100 M of NaOH
Consider the titration curves of four different acids titrated with a strong base 12.0 10.0 8.0 iv 6.0 pH 4.0 ii 2.0 10 50 20 30 40 Milliliters NaOH 60 Which acid has the smallest K, value? a. i b. ii c. iii d. iv
Fill out the tables below of the starting material and pure product by using the given NMR spectrums. Identify if the pure isomer of methyl nitrobenzoate as ortho, meta, or para. Complete the table below using your proton NMR spectrum of your starting material. Be sure to include all peaks. Note: The table is expandable. Use the structure below for the letter assignments in your table. Splitting Integration Assignment Peak (ppm) Other Notes -7.95 -7.92 0627 -787 785 7.30 751...
If the stock concentration for Thiosulfate is 0.1M, how would I find the delta (change in concentration) of thiosulfate in order to find the rate? Run Starch Color Time (mL) 0.2 M KNO: (ml) 9.5 8.0 6.5 5.0 3.5 0.20 M KI (mL) 2.5 4.0 5.5 0.025 M Na2S2O3 (mL) 2.5 2.5 2.5 2 3 0.5 0.5 0.5 0.1 M (NH4)2S2O8 (mL) 10.0 10.0 10.0 10.0 10.0 8:02 5:14 3:43 3:09 2:35 7.0 0.5 2.5 5 8.5 0.5 2.5 2.0...
5. Based on this analysis, the compound might be or contain the following substructure: 6. How many different types of carbons appear to be present? What are the chemical shifts for these carbons? UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
V. Draw the structures of Compound 23A (6 pts), Compound 23B (6 pts) and clearly indicate your assignments of all proton resonances using the lower case letter associated with the signal (6 pts). Calculate the Unsaturation Index of each compound (2 pts) (20 points total) 1.24 3.0 1.26 2.5 e = 1.25 ppm doublet, 6H 2.0 a = 10.0 ppm 1.5 Compound 23a: C10H420 singlet, 1H 10.00 7.83 7.85 7.09 7.07 1.0 Unsat. Index = (2C+2-H-X+N)/2 = X=number of halogens...
V. Draw the structures of Compound 23A (6 pts), Compound 23B (6 pts) and clearly indicate your assignments of all proton resonances using the lower case letter associated with the signal (6 pts). Calculate the Unsaturation Index of each compound (2 pts) (20 points total) 1.24 3.0 1.26 2.5 e = 1.25 ppm doublet, 6H 2.0 a = 10.0 ppm 1.5 Compound 23a: C10H420 singlet, 1H 10.00 7.83 7.85 7.09 7.07 1.0 Unsat. Index = (2C+2-H-X+N)/2 = X=number of halogens...
. Starting with equilibrium at zero, on the graph paper provided draw a transverse wave plitude of 3 units. Sketch three complete with a wavelength (a) of 6 units and an am waves and label them wave "A" of 4 units and an amplitude of 2. Starting with equilibrium at zero, draw a wave with a A 4 units. Sketch four complete waves and label them wave "B" When waves interfere with each other their amplitudes sum to the amplitude...
Below are pictures of my HNMR and CNMR for salenH2. I have already assigned some of the protons and carbons myself, but I am having trouble with the rest. As far as I know, there are 8 unique carbons and 7 unique hydrogens. The carbons are numbered and the hydrogens are lettered. I have included a labeled picture of the compound on each page. CNMR overall: CNMR zoomed: HNMR overall: HNMR zoomed: Thanks! (thousandths) 0 2.0 4.0 6.0 8.0 10.0...
SnowGeese File: Trial Diet WtChange DigEff ADFiber 1 Plants -6.0 0.0 28.5 2 Plants -5.0 2.5 27.5 3 Plants -4.5 5.0 27.5 4 Plants 0.0 0.0 32.5 5 Plants 2.0 0.0 32.0 6 Plants 3.5 1.0 30.0 7 Plants -2.0 2.5 34.0 8 Plants -2.5 10.0 36.5 9 Plants -3.5 20.0 28.5 10 Plants -2.5 12.5 29.0 11 Plants -3.0 28.0 28.0 12 Plants -8.5 30.0 28.0 13 Plants -3.5 18.0 30.0 14 Plants -3.0 15.0 31.0 15 Plants -2.5 ...