Title | Workshop 1 - teacher Zachary Katsamanis |
---|---|
Author | Vivian Lin |
Course | Organic Chemistry II |
Institution | Stony Brook University |
Pages | 3 |
File Size | 325.1 KB |
File Type | |
Total Downloads | 101 |
Total Views | 121 |
teacher Zachary Katsamanis...
1/31/2021
https://organic.cc.stonybrook.edu/che322-21/oscerfolio/example_002.php
Conjugated molecules Workshop 1
CHE 322 Organic Chemistry II Spring 2021
Question 1 Choose the order that has the following radicals correctly arranged with respect to increasing stability.
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Question 2 Choose the order that has the following carbocations correctly arranged with respect to increasing stability.
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Question 3 Choose the lowest unoccupied molecular orbital (LUMO) of the allyl cation.
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Question 4 Choose the order that has the following compounds correctly arranged with respect to increasing wavelength of their p --> p* absorptions in the UV-visible spectrum.
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Question 5 Choose the order that has the following compounds correctly arranged with respect to increasing wavelength of their p --> p* absorptions in the UV-visible spectrum.
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Question 6 Chapter 15 of your textbook discusses conjugation and various reactions of 1,3-dienes. In CHE 321, we discussed various ways to make alkenes, but we did not discuss methodology for making dienes. Fortunately, we can apply some of our standard CHE 321 reactions to this important problem. Choose the major product (compound A) of the following reaction sequence.
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Question 7 Select the major product of the following reaction sequence.
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Question 8 Select the correct missing reagent (compound X) of the following reaction sequence.
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Question 9 Select the carbocation that is expected to be the least stable.
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Question 10 Select the carbanion that is expected to be the most stable. https://organic.cc.stonybrook.edu/che322-21/oscerfolio/example_002.php
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Printed: Sunday 31st of January 2021.
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