Campbell Biology (11th Edition)
Campbell Biology (11th Edition)
11th Edition
ISBN: 9780134093413
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Jane B. Reece
Publisher: PEARSON
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Chapter 2, Problem 9TYU

DRAW IT Draw Lewis dot structures for each hypothetical molecule shown below, using the correct number of valence electrons for each atom. Determine which molecule makes sense because each atom has a complete valence shell and each bond has the correct number of electrons. Explain what makes the other molecule nonsensical, considering the number of bonds each type of atom can make.

(a)Chapter 2, Problem 9TYU, DRAW IT Draw Lewis dot structures for each hypothetical molecule shown below, using the correct , example  1

(b) Chapter 2, Problem 9TYU, DRAW IT Draw Lewis dot structures for each hypothetical molecule shown below, using the correct , example  2

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Convert the following structural formulas into condensed structures.
Butadiene (right) is a colorless gas used to make synthetic rubber and many other compounds. (a) How many σ bonds and π bonds does the molecule have? (b) Are cis-trans arrangements about the double bonds possible? Explain.
Unshared, or lone, electron pairs play an important role in determining the chemical and physical properties of organic compounds. Thus, it is important to know which atoms carry unshared pairs. Use the structural formulas below to determine the number of unshared pairs at each designated atom. Be sure your answers are consistent with the formal charges on the formulas. H₂C H₂ b Hc N CH2 The number of unshared pairs at atom a is The number of unshared pairs at atom b is The number of unshared pairs at atom c is The number of unshared pairs at atom a is 1 v The number of unshared pairs at atom b is Ov The number of unshared pairs at atom c is 1.

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Campbell Biology (11th Edition)

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