Lecture #18 | ||
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Lecture Outline | Review for Exam II | |
List of topics for EXAM II. | ![]() |
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What's expected for geometrical isomers for these two? | ![]() |
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There is more than one geometrical isomer that can be constructed at first. | ![]() |
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We will use VSEPR to determine bond angles in a
collection of different illustrations some of which are
shown here. In the first, all angles are 120o since the benzene ring, because of resonance, is a perfect hexagon with 120o internal angles. The second, after focussing attention on the N as a central atom has its lone pair compressing the other single bonds closer than their ideal 109.5o (despite having drawn the lone pair as if it were inside the ring -- which it isn't) |
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Examples | ![]() |
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Careful! | ![]() |
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Practice in finding structural isomers and finishing Lewis structure pictures. | ![]() |
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Expanded octet needed. | ![]() |
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Examples | ![]() |
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Examples | ![]() |
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Molecular basis of acid strength. The comparison is with selenic acid which is OSe(OH)3. This is a tougher level question for review purposes. | ![]() |
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