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Chapter 17, Unnumbered Figure 1, Page 706
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Chapter 17, Unnumbered Figure 2, Page 706
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Chapter 17, Unnumbered Figure 1, Page 708
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Chapter 17, Unnumbered Figure 2, Page 710
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Chapter 17, Unnumbered Figure 3, Page 710
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Chapter 17, Unnumbered Figure 10, Page 712
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Chapter 17, Figure 17.1 Bonding in a carbonyl group. The bond is formed by side-to-side overlap of a p orbital of carbon with a p orbital of oxygen.
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Chapter 17, Unnumbered Figure 1, Page 713
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Chapter 17, Unnumbered Figure 1, Page 714
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Chapter 17, Unnumbered Figure 2, Page 714
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Chapter 17, Unnumbered Figure 3, Page 714
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Chapter 17, Unnumbered Figure 4, Page 715
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Chapter 17, Unnumbered Figure 2, Page 717
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Chapter 17, Figure 17.2 Reaction coordinate diagrams for nucleophilic addition–elimination reactions with nucleophiles of varying basicity. (TI is the tetrahedral intermediate): (a) The nucleophile is a weaker base than the group attached to the acyl group in the reactant. (b) The nucleophile is a stronger base than the group attached to the acyl group in the reactant. (c) The nucleophile and the group attached to the acyl group in the reactant have similar basicities.
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Chapter 17, Figure 17.2A Reaction coordinate diagrams for nucleophilic addition–elimination reactions with nucleophiles of varying basicity. (TI is the tetrahedral intermediate): (a) The nucleophile is a weaker base than the group attached to the acyl group in the reactant. (b) The nucleophile is a stronger base than the group attached to the acyl group in the reactant. (c) The nucleophile and the group attached to the acyl group in the reactant have similar basicities.
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Chapter 17, Figure 17.2B Reaction coordinate diagrams for nucleophilic addition–elimination reactions with nucleophiles of varying basicity. (TI is the tetrahedral intermediate): (a) The nucleophile is a weaker base than the group attached to the acyl group in the reactant. (b) The nucleophile is a stronger base than the group attached to the acyl group in the reactant. (c) The nucleophile and the group attached to the acyl group in the reactant have similar basicities.
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Chapter 17, Figure 17.2C Reaction coordinate diagrams for nucleophilic addition–elimination reactions with nucleophiles of varying basicity. (TI is the tetrahedral intermediate): (a) The nucleophile is a weaker base than the group attached to the acyl group in the reactant. (b) The nucleophile is a stronger base than the group attached to the acyl group in the reactant. (c) The nucleophile and the group attached to the acyl group in the reactant have similar basicities.
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Chapter 17, Unnumbered Figure 1, Page 719
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Chapter 17, Unnumbered Figure 1, Page 720
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Chapter 17, Unnumbered Figure 2, Page 720
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Chapter 17, Unnumbered Figure 3, Page 720
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Chapter 17, Unnumbered Figure 4, Page 720
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Chapter 17, Unnumbered Figure 1, Page 721
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Chapter 17, Unnumbered Figure 2, Page 721
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Chapter 17, Unnumbered Figure 3, Page 721
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Chapter 17, Unnumbered Figure 8, Page 721
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Chapter 17, Unnumbered Figure 1, Page 722
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Chapter 17, Unnumbered Figure 2, Page 723
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Chapter 17, Unnumbered Figure 3, Page 723
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Chapter 17, Unnumbered Figure 2, Page 727
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Chapter 17, Unnumbered Figure 2, Page 728
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Chapter 17, Unnumbered Figure 3, Page 728
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Chapter 17, Unnumbered Figure 2, Page 730
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Chapter 17, Unnumbered Figure 5, Page 731
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Chapter 17, Unnumbered Figure 4, Page 732
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Chapter 17, Unnumbered Figure 3, Page 734
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Chapter 17, Unnumbered Figure 2, Page 736
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Chapter 17, Unnumbered Figure 1, Page 737
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Chapter 17, Unnumbered Figure 2, Page 737
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Chapter 17, Figure 17.4 In aqueous solution, soap forms micelles. The polar heads (carboxylate groups) of the soap molecules form the micelle’s outer surface; the nonpolar tails (fatty acid R groups) extend into the micelle’s interior.
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Chapter 17, Unnumbered Figure 3, Page 751
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Chapter 17, Unnumbered Figure 4, Page 751
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Chapter 17, Unnumbered Figure 5, Page 751
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Chapter 17, Unnumbered Figure 1, Page 752
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Chapter 17, Unnumbered Figure 2, Page 752
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Chapter 17, Unnumbered Figure 3, Page 752
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Chapter 17, Unnumbered Figure 4, Page 752
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