6th Edition

ISBN: 9781264094493

Author: SMITH

Publisher: MCG

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Textbook Question

Chapter 21.8, Problem 19P

How can pentan-2-one be converted into each compound?

a. Chapter 21.8, Problem 19P, Problem 23.18 How can pentan-2-one be converted into each compound?
a. b. c. d.
, example 1 b. c. d.

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Chapter 21.8, Problem 18P

Chapter 21.8, Problem 20P

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(f) SO: Best Lewis Structure 3 e group geometry:_ shape/molecular geometry:, (g) CF2CF2 Best Lewis Structure polarity: e group arrangement:_ shape/molecular geometry: (h) (NH4)2SO4 Best Lewis Structure polarity: e group arrangement: shape/molecular geometry: polarity: Sketch (with angles): Sketch (with angles): Sketch (with angles):

1. Problem Set 3b Chem 141 For each of the following compounds draw the BEST Lewis Structure then sketch the molecule (showing bond angles). Identify (i) electron group geometry (ii) shape around EACH central atom (iii) whether the molecule is polar or non-polar (iv) (a) SeF4 Best Lewis Structure e group arrangement:_ shape/molecular geometry: polarity: (b) AsOBr3 Best Lewis Structure e group arrangement:_ shape/molecular geometry: polarity: Sketch (with angles): Sketch (with angles):

(c) SOCI Best Lewis Structure 2 e group arrangement: shape/molecular geometry:_ (d) PCls Best Lewis Structure polarity: e group geometry:_ shape/molecular geometry:_ (e) Ba(BrO2): Best Lewis Structure polarity: e group arrangement: shape/molecular geometry: polarity: Sketch (with angles): Sketch (with angles): Sketch (with angles):

Chapter 21 Solutions

ORGANIC CHEMISTRY BOOK& SG/SM

Ch. 21.2 - Problem 23.1 Draw the enol or keto tautomer(s) of...Ch. 21.2 - Problem 23.3 When phenylacetaldehyde is dissolved...Ch. 21.3 - Prob. 5P Ch. 21.3 - Problem 23.5 Which bonds in the following...Ch. 21.3 - Prob. 7P Ch. 21.3 - Prob. 8P Ch. 21.3 - Prob. 9P Ch. 21.4 - Prob. 10P Ch. 21.5 - Prob. 11P Ch. 21.7 - Problem 23.11 Draw the products of each...

Ch. 21.7 - Problem 23.12 Draw the products of each reaction....Ch. 21.7 - Prob. 14P Ch. 21.7 - Prob. 15P Ch. 21.8 - Prob. 16P Ch. 21.8 - Prob. 17P Ch. 21.8 - Prob. 18P Ch. 21.8 - Problem 23.18 How can pentan-2-one be converted...Ch. 21.8 - Problem 23.19 Identify A, B, and C, intermediates...Ch. 21.9 - Problem 23.20 Which of the following compounds...Ch. 21.9 - Problem 23.21 Draw the products of each...Ch. 21.9 - Prob. 23P Ch. 21.9 - Prob. 24P Ch. 21.9 - Prob. 25P Ch. 21.10 - Prob. 26P Ch. 21.10 - Prob. 27P Ch. 21.10 - Prob. 28P Ch. 21.10 - Prob. 29P Ch. 21 - 23.29 Draw enol tautomer(s) for each compound....Ch. 21 - 22.30 The cis ketone A is isomerized to a trans...Ch. 21 - 23.31 Draw enol tautomer(s) for each compound. ...Ch. 21 - Prob. 33P Ch. 21 - Prob. 34P Ch. 21 - 23.35 Rank the labeled protons in each compound in...Ch. 21 - Prob. 36P Ch. 21 - Prob. 37P Ch. 21 - 23.38 Acyclovir is an effective antiviral agent...Ch. 21 - 23.39 Explain why forms two different alkylation...Ch. 21 - Prob. 40P Ch. 21 - 23.42 Draw a stepwise mechanism for the following...Ch. 21 - Prob. 42P Ch. 21 - Prob. 43P Ch. 21 - 23.45 Devise a synthesis of valproic acid , a...Ch. 21 - Prob. 57P Ch. 21 - 23.57 Draw a stepwise mechanism showing how two...Ch. 21 - 23.58 Draw a stepwise mechanism for the following...Ch. 21 - Prob. 65P Ch. 21 - 23.66 Synthesize (Z)-hept-5-en-2-one from ethyl...

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