EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
9th Edition
ISBN: 9780136781776
Author: Wade
Publisher: PEARSON CO
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Chapter 2.1B, Problem 2.3P

For each of the following compounds

  1. 1. Draw the Lewis structure.
  2. 2. Show how the bond dipole moments (and those of any nonbonding pairs of electrons) contribute to the molecular dipole moment.
  3. 3. Estimate whether the compound will have a large small, or zero dipole moment.
  4. a. NH4+
  5. b. O3
  6. a. NH4+ has four polar N—H bonds These bonds are probably more polarized than a typical N—H bond, because the N in NH4+ bears a formal positive charge Nevertheless, these four colar bonds have a symmetric tetrahedral arrangement so they cancel each other.

Chapter 2.1B, Problem 2.3P, For each of the following compounds 1. Draw the Lewis structure. 2. Show how the bond dipole moments , example  1

  1. b. Ozone (O3) is an sp2 hybrid structure with a lone pair on the central oxygen atom Therefore O3 must be bent. The resonance structures imply partia negatve charges on the outer oxygens and a partial positive charge on the central oxygen. The lone pair on the central oxygen cancels part, but not all, of the vector sum of the two O—O dipoles The resulting not d polo is relatively small.

Chapter 2.1B, Problem 2.3P, For each of the following compounds 1. Draw the Lewis structure. 2. Show how the bond dipole moments , example  2

  1. a. Ozone (O3) is an sp2 hybrid structure, with a lone pair on the central oxygon atom Therefore, O3 must be bent. The resonance structures imply partial negative charges on the outer oxygens end a partial positive charge on the central oxygen. The lone pair on the central oxygen cancels part but not all, of the vector sum of the two O—O dipoles The resulting net dipole is relatively small.

Chapter 2.1B, Problem 2.3P, For each of the following compounds 1. Draw the Lewis structure. 2. Show how the bond dipole moments , example  3

  1. b. CH2CI2
  2. c. CH3F
  3. d. CF4
  4. e. CH3OH
  5. f. HCN
  6. g. CH3CHO
  7. h. H2C=NH
  8. i. (CH3)3N
  9. j. CH2=CHCI
  10. k. BF3
  11. l. BeCl2
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Chapter 2 Solutions

EP ORGANIC CHEMISTRY -MOD.MASTERING 18W

Ch. 2.7 - Ethanol, methylamine. and acetic acid are all...Ch. 2.8 - Prob. 2.12PCh. 2.10 - Write equations for the following acid-base...Ch. 2.10 - Rank the following acids in decreasing order of...Ch. 2.11 - Prob. 2.15PCh. 2.11 - Prob. 2.16PCh. 2.11 - Consider each pair of bases and explain which one...Ch. 2.12 - Which is a stronger base ethoxide ion or acetate...Ch. 2.12 - Prob. 2.19PCh. 2.12 - Prob. 2.20PCh. 2.12 - Prob. 2.21PCh. 2.12 - Choose the more basic member of each pair of...Ch. 2.14 - Prob. 2.23PCh. 2.15D - Classify the following hydrocarbons and draw a...Ch. 2.16D - Prob. 2.25PCh. 2.17C - Draw a Lewis structure and classify each of the...Ch. 2.17C - Circle the functional groups in the following...Ch. 2 - The CN triple bond in acetonitrile has a dipole...Ch. 2 - Prob. 2.29SPCh. 2 - Sulfur dioxide has a dipole moment of 1.60 D....Ch. 2 - Which of the following pure compounds can form...Ch. 2 - Predict which member of each pair is more soluble...Ch. 2 - Prob. 2.33SPCh. 2 - Prob. 2.34SPCh. 2 - Predict which compound in each pair has the higher...Ch. 2 - All of the following compounds can react as acids...Ch. 2 - Rank the following species in order of increasing...Ch. 2 - Rank the following species in order of increasing...Ch. 2 - The Ka of phenylacetic acid is 5 2 105, and the...Ch. 2 - The following compound can become protonated on...Ch. 2 - The following compounds are listed in increasing...Ch. 2 - Prob. 2.42SPCh. 2 - Prob. 2.43SPCh. 2 - Compare the relative acidity of 1-molar aqueous...Ch. 2 - The following compounds can all react as acids. a....Ch. 2 - The following compounds can all react as bases. a....Ch. 2 - The following compounds can all react as acids. a....Ch. 2 - Prob. 2.48SPCh. 2 - Methyllithium (CH3Li) is often used as a base in...Ch. 2 - Label the reactants in these acid-base reactions...Ch. 2 - In each reaction, label the reactants as Lewis...Ch. 2 - Prob. 2.52SPCh. 2 - Each of these compounds can react as a nucleophile...Ch. 2 - Prob. 2.54SPCh. 2 - Give a definition and an example for each class of...Ch. 2 - Circle the functional groups in the following...Ch. 2 - Prob. 2.57SP
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