EBK ORGANIC CHEMISTRY
9th Edition
ISBN: 8220100591310
Author: McMurry
Publisher: CENGAGE L
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Textbook Question
Chapter 20.2, Problem 4P
The Ka for dichloroacetic acid is 3.32 Ă— 10-2. Approximately what percentage of the acid is dissociated in a 0.10 M aqueous solution?
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What is the pH of a buffer made from 0.350
mol of HBrO (Ka = 2.5 × 10-9) and 0.120
mol of KBRO in 2.0 L of solution?
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aw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant
rate under these conditions, check the box underneath the drawing area instead.
Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products.
Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but
strong heat or reflux is not used.
B
C
Br
HO
O Substitution will not occur at a significant rate.
Explanation
Check
+
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drawing a structure.
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Complete the following reactions with the necessary reagents to complete the shown
transformation.
Example:
1.
2.
?
3.
018
Br
OH
Answer: H₂O, H2SO4, HgSO4
Chapter 20 Solutions
EBK ORGANIC CHEMISTRY
Ch. 20.1 - Give IUPAC names for the following compounds:Ch. 20.1 - Draw structures corresponding to the following...Ch. 20.2 - Prob. 3PCh. 20.2 - The Ka for dichloroacetic acid is 3.32 Ă— 10-2....Ch. 20.3 - Calculate the percentages of dissociated and...Ch. 20.4 - Which would you expect to be a stronger acid, the...Ch. 20.4 - Dicarboxylic acids have two dissociation...Ch. 20.4 - The pKa of p-cyclopropylbenzoic acid is 4.45. Is...Ch. 20.4 - Prob. 9PCh. 20.5 - Prob. 10P
Ch. 20.6 - Prob. 11PCh. 20.6 - How might you carry out the following...Ch. 20.7 - Prob. 13PCh. 20.7 - Prob. 14PCh. 20.8 - Cyclopentanecarboxylic acid and...Ch. 20.8 - Prob. 16PCh. 20.SE - Prob. 17VCCh. 20.SE - Prob. 18VCCh. 20.SE - The following carboxylic acid can’t be prepared...Ch. 20.SE - Electrostatic potential maps of anisole and...Ch. 20.SE - Predict the product(s) and provide the mechanism...Ch. 20.SE - Predict the product(s) and provide the mechanism...Ch. 20.SE - Prob. 23MPCh. 20.SE - Predict the product(s) and provide the complete...Ch. 20.SE - Acid-catalyzed hydrolysis of a nitrile to give a...Ch. 20.SE - Prob. 26MPCh. 20.SE - Naturally occurring compounds called cyanogenic...Ch. 20.SE - 2-Bromo-6, 6-dimethylcyclohexanone gives 2,...Ch. 20.SE - Naturally occurring compounds called terpenoids,...Ch. 20.SE - In the Ritter reaction, an alkene reacts with a...Ch. 20.SE - Give IUPAC names for the following compounds:Ch. 20.SE - Prob. 32APCh. 20.SE - Prob. 33APCh. 20.SE - Prob. 34APCh. 20.SE - Prob. 35APCh. 20.SE - Prob. 36APCh. 20.SE - Prob. 37APCh. 20.SE - Prob. 38APCh. 20.SE - Calculate the Ka's for the following acids: (a)...Ch. 20.SE - Thioglycolic acid, HSCH2CO2H, a substance used in...Ch. 20.SE - Prob. 41APCh. 20.SE - Prob. 42APCh. 20.SE - How could you convert butanoic acid into the...Ch. 20.SE - How could you convert each of the following...Ch. 20.SE - How could you convert butanenitrile into the...Ch. 20.SE - How would you prepare the following compounds from...Ch. 20.SE - Prob. 47APCh. 20.SE - Using 13CO2 as your only source of labeled carbon,...Ch. 20.SE - Prob. 49APCh. 20.SE - Which method-Grignard carboxylation or nitrile...Ch. 20.SE - Prob. 51APCh. 20.SE - Prob. 52APCh. 20.SE - Propose a structure for a compound C6H12O2 that...Ch. 20.SE - Prob. 54APCh. 20.SE - How would you use NMR (either 13C or 1H) to...Ch. 20.SE - Prob. 56APCh. 20.SE - A chemist in need of 2,2-dimethylpentanoic acid...Ch. 20.SE - Prob. 58APCh. 20.SE - Prob. 59APCh. 20.SE - Prob. 60APCh. 20.SE - Prob. 61APCh. 20.SE - Prob. 62APCh. 20.SE - Prob. 63APCh. 20.SE - The following pKa values have been measured....Ch. 20.SE - Identify the missing reagents a-f in the following...Ch. 20.SE - Propose a structure for a compound, C4H7N, that...Ch. 20.SE - Prob. 67APCh. 20.SE - The 1H and 13C NMR spectra below belong to a...Ch. 20.SE - Propose structures for carboxylic acids that show...Ch. 20.SE - Carboxylic acids having a second carbonyl group...
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- 7:34 • < Question 18 of 22 5G 50% Submit What is the pH of a buffer made from 0.220 mol of HCNO (Ka = 3.5 × 10-4) and 0.410 mol of NaCNO in 2.0 L of solution? 1 2 3 ☑ 4 5 6 C 7 8 | 9 +/- 0 ×10 Tap here for additional resources ||| Гarrow_forward6:46 ✔ 5G 58% < Question 7 of 22 Submit What is the primary species in solution at the halfway point in a titration of NH3 with HBr? A NH3 and H+ B NH₁+ and H+ C NH4+ D NH3 and NH4+ Tap here for additional resources |||arrow_forward6:49 Dji < Question 15 of 22 4G 57% Submit The pOH of a solution is 10.50. What is the OH- concentration in the solution? A 3.2 × 10-4 M B C 3.2 x 10-11 M 10.50 M D 4.2 M E 3.50 M Tap here for additional resources |||arrow_forward
- ヨ 6:49 Dji < Question 13 of 22 5G 57% Submit The pH of a solution is 2.40. What is the H+ concentration in the solution? A B 2.5 x 10-12 M 4.0 × 10-3 M C 2.40 M D 4.76 M 11.60 M Tap here for additional resources |||arrow_forwardヨ C 6:48 Di✔ < Question 12 of 22 5G 57% Submit The pH of a solution is 12.50. What is the H+ concentration in the solution? A 0.032 M B 3.2 × 10-13 M 1.5 M D 9.25 M 12.50 M Tap here for additional resources |||arrow_forwardヨ C 6:48 Di✔ < Question 11 of 22 5G 57% Submit The pH of a solution is 1.50. What is the H+ concentration in the solution? A 0.032 M B 3.2 × 10-13 M 1.5 M D 2.15 M 12.50 M Tap here for additional resources |||arrow_forward
- Use excel to plot the following titration data. Once you have done your plot, make sure to label the axes correctly. Use your graph to determine the pK, for the weak acid. Attach your plot to the back of this worksheet. A 1.0M solution of weak acid was titrated with a base and the following data was collected. Equivalents of Base pH observed 0.05 3.4 0.15 3.9 0.25 4.2 0.40 4.5 0.60 4.9 0.75 5.2 0.85 5.4 0.95 6.0arrow_forward1. Write the dissociation reaction then calculate the pH for the following STRONG substances. a. 2.5x103 M HBr b.5.6x10 M NaOHarrow_forward74. A contour map for an atomic orbital of hydrogen is shown below for the xy and xz planes. Identify the type (s, p, d, f, g . . .) of orbital. axis x axis z axis Cooo xy planearrow_forward
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