Chemistry: An Atoms-Focused Approach
14th Edition
ISBN: 9780393912340
Author: Thomas R. Gilbert, Rein V. Kirss, Natalie Foster
Publisher: W. W. Norton & Company
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Chemistry: An Atoms-Focused Approach
Ch. 5 - Prob. 5.1VPCh. 5 - Prob. 5.2VPCh. 5 - Prob. 5.3VPCh. 5 - Prob. 5.4VPCh. 5 - Prob. 5.5VPCh. 5 - Prob. 5.6VPCh. 5 - Prob. 5.7VPCh. 5 - Prob. 5.8VPCh. 5 - Prob. 5.9VPCh. 5 - Prob. 5.10VP
Ch. 5 - Prob. 5.11QACh. 5 - Prob. 5.12QACh. 5 - Prob. 5.13QACh. 5 - Prob. 5.14QACh. 5 - Prob. 5.15QACh. 5 - Prob. 5.16QACh. 5 - Prob. 5.17QACh. 5 - Prob. 5.18QACh. 5 - Prob. 5.19QACh. 5 - Prob. 5.20QACh. 5 - Prob. 5.21QACh. 5 - Prob. 5.22QACh. 5 - Prob. 5.23QACh. 5 - Prob. 5.24QACh. 5 - Prob. 5.25QACh. 5 - Prob. 5.26QACh. 5 - Prob. 5.27QACh. 5 - Prob. 5.28QACh. 5 - Prob. 5.29QACh. 5 - Prob. 5.30QACh. 5 - Prob. 5.31QACh. 5 - Prob. 5.32QACh. 5 - Prob. 5.33QACh. 5 - Prob. 5.34QACh. 5 - Prob. 5.35QACh. 5 - Prob. 5.36QACh. 5 - Prob. 5.37QACh. 5 - Prob. 5.38QACh. 5 - Prob. 5.39QACh. 5 - Prob. 5.40QACh. 5 - Prob. 5.41QACh. 5 - Prob. 5.42QACh. 5 - Prob. 5.43QACh. 5 - Prob. 5.44QACh. 5 - Prob. 5.45QACh. 5 - Prob. 5.46QACh. 5 - Prob. 5.47QACh. 5 - Prob. 5.48QACh. 5 - Prob. 5.49QACh. 5 - Prob. 5.50QACh. 5 - Prob. 5.51QACh. 5 - Prob. 5.52QACh. 5 - Prob. 5.54QACh. 5 - Prob. 5.55QACh. 5 - Prob. 5.56QACh. 5 - Prob. 5.57QACh. 5 - Prob. 5.58QACh. 5 - Prob. 5.59QACh. 5 - Prob. 5.60QACh. 5 - Prob. 5.61QACh. 5 - Prob. 5.62QACh. 5 - Prob. 5.63QACh. 5 - Prob. 5.64QACh. 5 - Prob. 5.65QACh. 5 - Prob. 5.66QACh. 5 - Prob. 5.67QACh. 5 - Prob. 5.68QACh. 5 - Prob. 5.69QACh. 5 - Prob. 5.70QACh. 5 - Prob. 5.71QACh. 5 - Prob. 5.72QACh. 5 - Prob. 5.73QACh. 5 - Prob. 5.74QACh. 5 - Prob. 5.75QACh. 5 - Prob. 5.76QACh. 5 - Prob. 5.77QACh. 5 - Prob. 5.78QACh. 5 - Prob. 5.79QACh. 5 - Prob. 5.80QACh. 5 - Prob. 5.81QACh. 5 - Prob. 5.82QACh. 5 - Prob. 5.83QACh. 5 - Prob. 5.84QACh. 5 - Prob. 5.85QACh. 5 - Prob. 5.86QACh. 5 - Prob. 5.87QACh. 5 - Prob. 5.88QACh. 5 - Prob. 5.89QACh. 5 - Prob. 5.90QACh. 5 - Prob. 5.91QACh. 5 - Prob. 5.92QACh. 5 - Prob. 5.93QACh. 5 - Prob. 5.94QACh. 5 - Prob. 5.95QACh. 5 - Prob. 5.96QACh. 5 - Prob. 5.97QACh. 5 - Prob. 5.98QACh. 5 - Prob. 5.99QACh. 5 - Prob. 5.100QACh. 5 - Prob. 5.101QACh. 5 - Prob. 5.102QACh. 5 - Prob. 5.103QACh. 5 - Prob. 5.104QACh. 5 - Prob. 5.105QACh. 5 - Prob. 5.106QACh. 5 - Prob. 5.107QACh. 5 - Prob. 5.108QACh. 5 - Prob. 5.109QACh. 5 - Prob. 5.110QACh. 5 - Prob. 5.111QACh. 5 - Prob. 5.112QACh. 5 - Prob. 5.113QACh. 5 - Prob. 5.114QACh. 5 - Prob. 5.115QACh. 5 - Prob. 5.116QACh. 5 - Prob. 5.117QACh. 5 - Prob. 5.118QACh. 5 - Prob. 5.119QACh. 5 - Prob. 5.120QACh. 5 - Prob. 5.121QACh. 5 - Prob. 5.122QACh. 5 - Prob. 5.123QACh. 5 - Prob. 5.124QACh. 5 - Prob. 5.125QACh. 5 - Prob. 5.126QACh. 5 - Prob. 5.127QACh. 5 - Prob. 5.128QACh. 5 - Prob. 5.129QACh. 5 - Prob. 5.130QACh. 5 - Prob. 5.131QACh. 5 - Prob. 5.132QA
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- It is possible to write a simple Lewis structure for the SO42- ion, involving only single bonds, which follows the octet rule. However, Linus Pauling and others have suggested an alternative structure, involving double bonds, in which the sulfur atom is surrounded by six electron pairs. (a) Draw the two Lewis structures. (b) What geometries are predicted for the two structures? (c) What is the hybridization of sulfur in each case? (d) What are the formal charges of the atoms in the two structures?arrow_forwardThe bond length in C2 is 131 pm. Compare this with the bond lengths in C2H2 (120 pm), C2H4 (134 pm), and C2H6 (153 pm). What bond order would you predict for C2 from its bond length? Does this agree with the molecular orbital configuration you would predict for C2?arrow_forwardThe sulfamate ion, H2NSO3, can be thought of as having been formed from the amide ion, NH2, and sulphur trioxide, SO3. (a) What are the electron-pair and molecular geometries or the amide ion and or SO3? What are the hybridizations of the N and S atoms, respectively? (b) Sketch a structure for the sulfamate ion, and estimate the bond angles. (c) What changes in hybridization do you expect for N and S in the course of the reaction NH2 + SO3 H2NSO3? (d) Is SO3 the donor of an electron pair or the acceptor of an electron pair in the reaction with amide ion? Does the electrostatic potential map shown below confirm your prediction?arrow_forward
- Minoxidil (C9H15N15O) is a compound produced by the Pharmacia Upjohn Company that has been approved as a treatment for some types of male pattern baldness. Note that in such shorthand ring structures, each point where lines meet is a carbon atom and that the hydrogen atoms bonded to the carbon atoms in the rings have been omitted. There will be four bonds to each carbon atom. a. Give the hybridization of the five nitrogen atoms in minoxidil. b. Give the hybridization of each of the nine carbon atoms in minoxidil. c. Give the approximate values for the bond angles marked a, b, c, d, e, and f. d. Including all the hydrogen atoms, how many bonds exist in minoxidil? e. How many bonds exist in minoxidil?arrow_forwardExplain in terms of bonding theory why all four hydrogen atoms of allene, H2CCCH2, cannot lie in the same plane.arrow_forwardAspirin, or acetylsalicylic acid, has the formula C9H8O4 and the skeleton structure (a) Complete the Lewis structure and give the number of bonds and bonds in aspirin. (b) What is the hybridization about the CO2H carbon atom (colored blue)? (c) What is the hybridization about the carbon atom in the benzene-like ring that is bonded to an oxygen atom (colored red)? Also, what is the hybridization of the oxygen atom bonded to this carbon atom?arrow_forward
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