Chemistry: An Atoms-Focused Approach (Second Edition)
2nd Edition
ISBN: 9780393614053
Author: Thomas R. Gilbert, Rein V. Kirss, Stacey Lowery Bretz, Natalie Foster
Publisher: W. W. Norton & Company
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Q2: Draw the molecules based on the provided nomenclatures below:
(2R,3S)-2-chloro-3-methylpentane:
(2S, 2R)-2-hydroxyl-3,6-dimethylheptane:
Q3: Describes the relationship (identical, constitutional isomers, enantiomers or diastereomers)
of each pair of compounds below.
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Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label
each compound as chiral or achiral.
OH
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Chapter 15 Solutions
Chemistry: An Atoms-Focused Approach (Second Edition)
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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- These are synthesis questions. You need to show how the starting material can be converted into the product(s) shown. You may use any reactions we have learned. Show all the reagents you need. Show each molecule synthesized along the way and be sure to pay attention to the regiochemistry and stereochemistry preferences for each reaction. If a racemic molecule is made along the way, you need to draw both enantiomers and label the mixture as "racemic". All of the carbon atoms of the products must come from the starting material! ? H Harrow_forwardQ5: Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Clearly show stereochemistry by drawing the wedge-and-dashed bonds. Describe the relationship between each pair of the stereoisomers you have drawn.arrow_forwardClassify each pair of molecules according to whether or not they can participate in hydrogen bonding with one another. Participate in hydrogen bonding CH3COCH3 and CH3COCH2CH3 H2O and (CH3CH2)2CO CH3COCH3 and CH₂ CHO Answer Bank Do not participate in hydrogen bonding CH3CH2OH and HCHO CH3COCH2CH3 and CH3OHarrow_forward
- Nonearrow_forwardGiven the standard enthalpies of formation for the following substances, determine the reaction enthalpy for the following reaction. 4A (g) + 2B (g) → 2C (g) + 7D (g) AHrxn =?kJ Substance AH in kJ/mol A (g) - 20.42 B (g) + 32.18 C (g) - 72.51 D (g) - 17.87arrow_forwardDetermine ASran for Zn(s) + 2HCl(aq) = ZnCl2(aq) + H2(aq) given the following information: Standard Entropy Values of Various Substance Substance So (J/mol • K) 60.9 Zn(s) HCl(aq) 56.5 130.58 H2(g) Zn2+(aq) -106.5 55.10 CI (aq)arrow_forward
- 3) Catalytic hydrogenation of the compound below produced the expected product. However, a byproduct with molecular formula C10H12O is also formed in small quantities. What is the by product?arrow_forwardWhat is the ΔHorxn of the reaction? NaOH(aq) + HCl(aq) → H2O(l) + NaCl(aq) ΔHorxn 1= ________ kJ/molarrow_forward= +92kJ ΔΗ = +170kJ Use the following reactions: 2NH3(9) N2(g) + 3H2(g) → 11/N2(g) + 2H2O (1) → NO2(g) + 2H2(g) Determine the DH° of this reaction: NO2(g) + H2(g) → 2(g) → 2H2O(l) + NH3(9) ΔΗarrow_forward
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