SMARTWORKS FOR CHEMISTRY: ATOMS FOCUSED
2nd Edition
ISBN: 9780393644777
Author: Gilbert
Publisher: MCGRAW-HILL HIGHER EDUCATION
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Chapter 15, Problem 15.91QA
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Diels Alder Cycloaddition: Focus on regiochemistry (problems E-F) –> match + of thedienophile and - of the diene while also considering stereochemistry (endo).
HELP! URGENT! PLEASE RESOND ASAP!
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
Chapter 15 Solutions
SMARTWORKS FOR CHEMISTRY: ATOMS FOCUSED
Ch. 15 - Prob. 15.1VPCh. 15 - Prob. 15.2VPCh. 15 - Prob. 15.3VPCh. 15 - Prob. 15.4VPCh. 15 - Prob. 15.5VPCh. 15 - Prob. 15.6VPCh. 15 - Prob. 15.7VPCh. 15 - Prob. 15.8VPCh. 15 - Prob. 15.9VPCh. 15 - Prob. 15.10VP
Ch. 15 - Prob. 15.11QACh. 15 - Prob. 15.12QACh. 15 - Prob. 15.13QACh. 15 - Prob. 15.14QACh. 15 - Prob. 15.15QACh. 15 - Prob. 15.16QACh. 15 - Prob. 15.17QACh. 15 - Prob. 15.18QACh. 15 - Prob. 15.19QACh. 15 - Prob. 15.20QACh. 15 - Prob. 15.21QACh. 15 - Prob. 15.22QACh. 15 - Prob. 15.23QACh. 15 - Prob. 15.24QACh. 15 - Prob. 15.25QACh. 15 - Prob. 15.26QACh. 15 - Prob. 15.27QACh. 15 - Prob. 15.28QACh. 15 - Prob. 15.29QACh. 15 - Prob. 15.30QACh. 15 - Prob. 15.31QACh. 15 - Prob. 15.32QACh. 15 - Prob. 15.33QACh. 15 - Prob. 15.34QACh. 15 - Prob. 15.35QACh. 15 - Prob. 15.36QACh. 15 - Prob. 15.37QACh. 15 - Prob. 15.38QACh. 15 - Prob. 15.39QACh. 15 - Prob. 15.40QACh. 15 - Prob. 15.41QACh. 15 - Prob. 15.42QACh. 15 - Prob. 15.43QACh. 15 - Prob. 15.44QACh. 15 - Prob. 15.45QACh. 15 - Prob. 15.46QACh. 15 - Prob. 15.47QACh. 15 - Prob. 15.48QACh. 15 - Prob. 15.49QACh. 15 - Prob. 15.50QACh. 15 - Prob. 15.51QACh. 15 - Prob. 15.52QACh. 15 - Prob. 15.53QACh. 15 - Prob. 15.54QACh. 15 - Prob. 15.55QACh. 15 - Prob. 15.56QACh. 15 - Prob. 15.57QACh. 15 - Prob. 15.58QACh. 15 - Prob. 15.59QACh. 15 - Prob. 15.60QACh. 15 - Prob. 15.61QACh. 15 - Prob. 15.62QACh. 15 - Prob. 15.63QACh. 15 - Prob. 15.64QACh. 15 - Prob. 15.65QACh. 15 - Prob. 15.66QACh. 15 - Prob. 15.67QACh. 15 - Prob. 15.68QACh. 15 - Prob. 15.69QACh. 15 - Prob. 15.70QACh. 15 - Prob. 15.71QACh. 15 - Prob. 15.72QACh. 15 - Prob. 15.73QACh. 15 - Prob. 15.74QACh. 15 - Prob. 15.75QACh. 15 - Prob. 15.76QACh. 15 - Prob. 15.77QACh. 15 - Prob. 15.78QACh. 15 - Prob. 15.79QACh. 15 - Prob. 15.80QACh. 15 - Prob. 15.81QACh. 15 - Prob. 15.82QACh. 15 - Prob. 15.83QACh. 15 - Prob. 15.84QACh. 15 - Prob. 15.85QACh. 15 - Prob. 15.86QACh. 15 - Prob. 15.87QACh. 15 - Prob. 15.88QACh. 15 - Prob. 15.89QACh. 15 - Prob. 15.90QACh. 15 - Prob. 15.91QACh. 15 - Prob. 15.92QACh. 15 - Prob. 15.93QACh. 15 - Prob. 15.94QACh. 15 - Prob. 15.95QACh. 15 - Prob. 15.96QACh. 15 - Prob. 15.97QACh. 15 - Prob. 15.98QACh. 15 - Prob. 15.99QACh. 15 - Prob. 15.100QACh. 15 - Prob. 15.101QACh. 15 - Prob. 15.102QACh. 15 - Prob. 15.103QACh. 15 - Prob. 15.104QACh. 15 - Prob. 15.105QACh. 15 - Prob. 15.106QACh. 15 - Prob. 15.107QACh. 15 - Prob. 15.108QACh. 15 - Prob. 15.109QACh. 15 - Prob. 15.110QA
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Similar questions
- 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 0.267arrow_forwardDraw 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 ઘarrow_forwardCalculate 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_forward
- Problem 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_forward2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forward
- Steps 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_forwardSteps and explanationn please.arrow_forward
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