Chapter 1: Problem 39
Use VSEPR to predict bond angles about each atom of carbon, nitrogen, and oxygen in these molecules. a. b. c. d. e. f.
Chapter 1: Problem 39
Use VSEPR to predict bond angles about each atom of carbon, nitrogen, and oxygen in these molecules. a. b. c. d. e. f.
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Get started for freeDraw structural formulas for the three tertiary \(\left(3^{\circ}\right)\) amines with the molecular formula \(\mathrm{C}_{5} \mathrm{H}_{13} \mathrm{~N}\).
Draw Lewis structures and condensed structural formulas for the four alcohols with the molecular formula \(\mathrm{C}_{4} \mathrm{H}_{10} \mathrm{O}\). Classify each alcohol as primary, secondary, or tertiary.
Draw Lewis structures, showing all valence electrons, for these molecules. (a) \(\mathrm{C}_{2} \mathrm{H}_{6}\) (b) \(\mathrm{CS}_{2}\) (c) \(\mathrm{HCN}\)
Cyanic acid, HOCN, and isocyanic acid, HNCO, dissolve in water to yield the same anion on loss of \(\mathrm{H}^{+}\). (a) Write a Lewis structure for cyanic acid. (b) Write a Lewis structure for isocyanic acid. (c) Account for the fact that each acid gives the same anion on loss of \(\mathrm{H}^{+}\). 1.71 In Chapter 6, we study a group of organic cations called carbocations. Following is the structure of one such carbocation, the tert-butyl cation. (a) How many electrons are in the valence shell of the carbon bearing the positive charge? (b) Using VSEPR, predict the bond angles about this carbon. (c) Given the bond angle you predicted in (b), what hybridization do you predict for this carbon?
Classify each bond as nonpolar covalent or polar covalent or state that ions are formed. (a) \(\mathrm{S}-\mathrm{H}\) (b) \(\mathrm{P}-\mathrm{H}\) (c) \(\mathrm{C}-\mathrm{F}\) (d) \(\mathrm{C}-\mathrm{Cl}\)
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