Chemistry
7th Edition
ISBN: 9780321940872
Author: John E. McMurry, Robert C. Fay, Jill Kirsten Robinson
Publisher: PEARSON
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Chapter 17, Problem 17.30CP
What are the signs (+, —, or 0) of
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Question 4
Determine the rate order and rate constant for sucrose hydrolysis.
Time (hours)
[C6H12O6]
0
0.501
0.500
0.451
1.00
0.404
1.50
0.363
3.00
0.267
First-order, k = 0.210 hour 1
First-order, k = 0.0912 hour 1
O Second-order, k =
0.590 M1 hour 1
O Zero-order, k = 0.0770 M/hour
O Zero-order, k = 0.4896 M/hour
O Second-order, k = 1.93 M-1-hour 1
10 pts
Determine the rate order and rate constant for sucrose hydrolysis.
Time (hours)
[C6H12O6]
0
0.501
0.500
0.451
1.00
0.404
1.50
0.363
3.00
0.267
Draw the products of the reaction shown below. Use wedge and dash bonds
to indicate stereochemistry. Ignore inorganic byproducts.
OSO4 (cat)
(CH3)3COOH
Select to Draw
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Chapter 17 Solutions
Chemistry
Ch. 17 - Prob. 17.1PCh. 17 - Prob. 17.2PCh. 17 - Prob. 17.3ACh. 17 - Prob. 17.4PCh. 17 - Prob. 17.5PCh. 17 - Prob. 17.6ACh. 17 - Prob. 17.7PCh. 17 - Prob. 17.8ACh. 17 - Prob. 17.9PCh. 17 - APPLY 17.10 Use the values of Hf and S in Appendix...
Ch. 17 - Prob. 17.11PCh. 17 - Conceptual APPLY 17.12 What are the signs (+, -,...Ch. 17 - PRACTICE 17.13 Consider the thermal decomposition...Ch. 17 - Prob. 17.14ACh. 17 - Prob. 17.15PCh. 17 - Prob. 17.16ACh. 17 - Prob. 17.17PCh. 17 - Prob. 17.18ACh. 17 - Prob. 17.19PCh. 17 - Prob. 17.20ACh. 17 - Prob. 17.21PCh. 17 - APPLY 17.22 If the vapour pressure of ethanol (...Ch. 17 - Prob. 17.23PCh. 17 - Prob. 17.24PCh. 17 - Prob. 17.25PCh. 17 - Prob. 17.26PCh. 17 - Prob. 17.27PCh. 17 - 17.28 Consider the gas-phase reaction of AB3 and...Ch. 17 - 17.29 Ideal gases A (red spheres) and B (blue...Ch. 17 - What are the signs (+, —, or 0) of H, S, and G...Ch. 17 - Prob. 17.31CPCh. 17 - Prob. 17.32CPCh. 17 - 17.33 Consider the following spontaneous reaction...Ch. 17 - Prob. 17.34CPCh. 17 - Consider again the dissociation reaction A2g 2...Ch. 17 - Prob. 17.36CPCh. 17 - Prob. 17.37CPCh. 17 - Prob. 17.38CPCh. 17 - Prob. 17.39CPCh. 17 - Which of the following processes are spontaneous,...Ch. 17 - Prob. 17.41SPCh. 17 - Assuming that gaseous reactants and products are...Ch. 17 - Prob. 17.43SPCh. 17 - Prob. 17.44SPCh. 17 - Prob. 17.45SPCh. 17 - 17.46 Predict the sign of the entropy change in...Ch. 17 - Predict the sign of S in the system for each of...Ch. 17 - Prob. 17.48SPCh. 17 - Prob. 17.49SPCh. 17 - Prob. 17.50SPCh. 17 - Prob. 17.51SPCh. 17 - Prob. 17.52SPCh. 17 - Prob. 17.53SPCh. 17 - Prob. 17.54SPCh. 17 - Prob. 17.55SPCh. 17 - Prob. 17.56SPCh. 17 - Prob. 17.57SPCh. 17 - Prob. 17.58SPCh. 17 - Prob. 17.59SPCh. 17 - Prob. 17.60SPCh. 17 - Prob. 17.61SPCh. 17 - Prob. 17.62SPCh. 17 - Prob. 17.63SPCh. 17 - Prob. 17.64SPCh. 17 - Prob. 17.65SPCh. 17 - Prob. 17.66SPCh. 17 - Prob. 17.67SPCh. 17 - Prob. 17.68SPCh. 17 - Prob. 17.69SPCh. 17 - Prob. 17.70SPCh. 17 - Prob. 17.71SPCh. 17 - Prob. 17.72SPCh. 17 - Prob. 17.73SPCh. 17 - Prob. 17.74SPCh. 17 - Prob. 17.75SPCh. 17 - Prob. 17.76SPCh. 17 - Prob. 17.77SPCh. 17 - Prob. 17.78SPCh. 17 - Prob. 17.79SPCh. 17 - Prob. 17.80SPCh. 17 - Prob. 17.81SPCh. 17 - Prob. 17.82SPCh. 17 - Prob. 17.83SPCh. 17 - Prob. 17.84SPCh. 17 - Prob. 17.85SPCh. 17 - Prob. 17.86SPCh. 17 - Prob. 17.87SPCh. 17 - Prob. 17.88SPCh. 17 - Prob. 17.89SPCh. 17 - Prob. 17.90SPCh. 17 - Prob. 17.91SPCh. 17 - Use the data in Appendix B to calculate H° and ...Ch. 17 - Prob. 17.93SPCh. 17 - Prob. 17.94SPCh. 17 - Prob. 17.95SPCh. 17 - Prob. 17.96SPCh. 17 - Prob. 17.97SPCh. 17 - Use the values of G°, in Appendix B to calculate...Ch. 17 - Prob. 17.99SPCh. 17 - Prob. 17.100SPCh. 17 - Prob. 17.101SPCh. 17 - Prob. 17.102SPCh. 17 - Prob. 17.103SPCh. 17 - Prob. 17.104SPCh. 17 - Prob. 17.105SPCh. 17 - Prob. 17.106SPCh. 17 - Prob. 17.107SPCh. 17 - Prob. 17.108SPCh. 17 - Prob. 17.109SPCh. 17 - Prob. 17.110SPCh. 17 - Prob. 17.111SPCh. 17 - Prob. 17.112SPCh. 17 - Prob. 17.113SPCh. 17 - Prob. 17.114SPCh. 17 - Prob. 17.115SPCh. 17 - Prob. 17.116SPCh. 17 - Prob. 17.117SPCh. 17 - Prob. 17.118SPCh. 17 - Prob. 17.119SPCh. 17 - Prob. 17.120CPCh. 17 - Prob. 17.121CPCh. 17 - Prob. 17.122CPCh. 17 - Prob. 17.123CPCh. 17 - Prob. 17.124CPCh. 17 - Prob. 17.125CPCh. 17 - Prob. 17.126CPCh. 17 - Prob. 17.127CPCh. 17 - Prob. 17.128CPCh. 17 - Prob. 17.129CPCh. 17 - Prob. 17.130CPCh. 17 - Use the data in Appendix B to calculate H°, S°,...Ch. 17 - Prob. 17.132CPCh. 17 - Prob. 17.133CPCh. 17 - Nickel tetracarbonyl, a volatile liquid used to...Ch. 17 - Prob. 17.135CPCh. 17 - Prob. 17.136CPCh. 17 - Prob. 17.137CPCh. 17 - Prob. 17.138CPCh. 17 - Prob. 17.139CPCh. 17 - Prob. 17.140CPCh. 17 - Prob. 17.141CPCh. 17 - Prob. 17.142CPCh. 17 - Prob. 17.143CPCh. 17 - Prob. 17.144CPCh. 17 - Prob. 17.145CPCh. 17 - Prob. 17.146CPCh. 17 - Consider the equilibriumN2O42NO2g. (a) Use the...Ch. 17 - Prob. 17.148MPCh. 17 - Prob. 17.149MPCh. 17 - Prob. 17.150MPCh. 17 - Prob. 17.151MPCh. 17 - Prob. 17.152MPCh. 17 - Prob. 17.153MPCh. 17 - Prob. 17.154MPCh. 17 - Prob. 17.155MP
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- Calculate the reaction rate for selenious acid, H2SeO3, if 0.1150 M I-1 decreases to 0.0770 M in 12.0 minutes. H2SeO3(aq) + 6I-1(aq) + 4H+1(aq) ⟶ Se(s) + 2I3-1(aq) + 3H2O(l)arrow_forwardProblem 5-31 Which of the following objects are chiral? (a) A basketball (d) A golf club (b) A fork (c) A wine glass (e) A spiral staircase (f) A snowflake Problem 5-32 Which of the following compounds are chiral? Draw them, and label the chirality centers. (a) 2,4-Dimethylheptane (b) 5-Ethyl-3,3-dimethylheptane (c) cis-1,4-Dichlorocyclohexane Problem 5-33 Draw chiral molecules that meet the following descriptions: (a) A chloroalkane, C5H11Cl (c) An alkene, C6H12 (b) An alcohol, C6H140 (d) An alkane, C8H18 Problem 5-36 Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. How H3C CH3 many chirality centers does erythronolide B have? OH Identify them. H3C -CH3 OH Erythronolide B H3C. H3C. OH OH CH3arrow_forwardPLEASE HELP! URGENT! PLEASE RESPOND!arrow_forward
- 2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forwardSteps and explanationn please.arrow_forwardProblem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂Harrow_forward
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