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Which resonance form contributes more to the resonance hybrid? Explain briefly. N-H H- CH3 H-ö CH3 Which of the following is NOT a resonance form of the compound given above? CH3 Y CH3 A) A) X because carbon better handles + charge (C less electronegative) B) B) Y because oxygen better handles + charge (O more electronegative) C) Y because oxygen better handles + charge (O is larger). N-H D) X because Y is missing an octet. D) E) Y because X is missing an octet. Identify the hybridization for cach of the following indicated atoms. Which of the following is the most accurate 3-Drepresentation of phenylacetylene. (lgnore resonance delkocalization; sketch just the discreet Lewis structure piven below.) H-O-H ÇECH A) sp sp phenylacetylene B) sp C) sp sp D) sp? sp? ĐAll of the above are accurate 3-D sketiches sp

Which resonance form contributes more to the resonance hybrid? Explain briefly. N-H H- CH3 H-ö CH3 Which of the following is NOT a resonance form of the compound given above? CH3 Y CH3 A) A) X because carbon better handles + charge (C less electronegative) B) B) Y because oxygen better handles + charge (O more electronegative) C) Y because oxygen better handles + charge (O is larger). N-H D) X because Y is missing an octet. D) E) Y because X is missing an octet. Identify the hybridization for cach of the following indicated atoms. Which of the following is the most accurate 3-Drepresentation of phenylacetylene. (lgnore resonance delkocalization; sketch just the discreet Lewis structure piven below.) H-O-H ÇECH A) sp sp phenylacetylene B) sp C) sp sp D) sp? sp? ĐAll of the above are accurate 3-D sketiches sp

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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b Verify Email | bartleby O Dashboard O Course: Chem 120 - Organic Che X O LOCAL clicker + A cpp.edu/~Isstarkey/local/clicker/bonding/resonance.html Which resonance form contributes more to the resonance hybrid? Explain briefly. N-H „CH3 H-ö. CH3 Which of the following is NOT a resonance form of the compound given above? ČH3 Y CH3 A) N-H A) X because carbon better handles + charge (C less electronegative) В) B) Y because oxygen better handles + charge (O more electronegative) `N-H C) Y because oxygen better handles + charge (O is larger). C) N-H D) X because Y is missing an octet. D) N-H E) Y because X is missing an octet. *1 Identify the hybridization for each of the following indicated atoms. Which of the t (Ignore re iowing is the moug sketch just the discreet Lewis structure given below.) H-O-H CH,CCH, ÇECH A) sp sp sp phenylacetylene B) sp? sp sp B) C) C) sp sp sp D) sp sp sp2 E) sp sp E) All of the above are accurate 3-D sketches Sp2 hp 10:06 AM 1 l ENG 2/23/2021
Transcribed Image Text:b Verify Email | bartleby O Dashboard O Course: Chem 120 - Organic Che X O LOCAL clicker + A cpp.edu/~Isstarkey/local/clicker/bonding/resonance.html Which resonance form contributes more to the resonance hybrid? Explain briefly. N-H „CH3 H-ö. CH3 Which of the following is NOT a resonance form of the compound given above? ČH3 Y CH3 A) N-H A) X because carbon better handles + charge (C less electronegative) В) B) Y because oxygen better handles + charge (O more electronegative) `N-H C) Y because oxygen better handles + charge (O is larger). C) N-H D) X because Y is missing an octet. D) N-H E) Y because X is missing an octet. *1 Identify the hybridization for each of the following indicated atoms. Which of the t (Ignore re iowing is the moug sketch just the discreet Lewis structure given below.) H-O-H CH,CCH, ÇECH A) sp sp sp phenylacetylene B) sp? sp sp B) C) C) sp sp sp D) sp sp sp2 E) sp sp E) All of the above are accurate 3-D sketches Sp2 hp 10:06 AM 1 l ENG 2/23/2021
b Verify Email | bartleby O Dashboard O Course: Chem 120 - Organic Che X O LOCAL clicker + A cpp.edu/~Isstarkey/local/clicker/bonding/resonance.html D) sp sp3 sp? E) sp2 sp2 sp? E) All of the above are accurate 3-D sketches. Identify each of the lone pairs in fentanyl as localized or delocalized. Identify the orbital occupied by the lone pair on each of the indicated nitrogen atoms in nicotine. CH3.. 2 :N- 1 :N fentanyl nicotine 2 3 A) localized delocalized localized 2 A) sp? B) delocalized localized localized В) Sp3 C) localized delocalized delocalized C) sp? Sp3 D) delocalized delocalized localized D) sp? sp? E) delocalized delocalized delocalized E) sp? *1 *Contributors: (1) Starkey Last updated January 2019 hp 10:07 AM I ll ENG 2/23/2021
Transcribed Image Text:b Verify Email | bartleby O Dashboard O Course: Chem 120 - Organic Che X O LOCAL clicker + A cpp.edu/~Isstarkey/local/clicker/bonding/resonance.html D) sp sp3 sp? E) sp2 sp2 sp? E) All of the above are accurate 3-D sketches. Identify each of the lone pairs in fentanyl as localized or delocalized. Identify the orbital occupied by the lone pair on each of the indicated nitrogen atoms in nicotine. CH3.. 2 :N- 1 :N fentanyl nicotine 2 3 A) localized delocalized localized 2 A) sp? B) delocalized localized localized В) Sp3 C) localized delocalized delocalized C) sp? Sp3 D) delocalized delocalized localized D) sp? sp? E) delocalized delocalized delocalized E) sp? *1 *Contributors: (1) Starkey Last updated January 2019 hp 10:07 AM I ll ENG 2/23/2021
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