More Practice Synthesis Problems

More Practice Synthesis Problems - O O OH D D 6. Show how...

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More Practice Synthesis Problems 1. Show how you would prepare the following compounds from the indicated starting materials. You may use any addition reagents you like unless otherwise restricted. a. OH OH O b. O O
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2. Show the detailed mechanism for the cyclic ester formation. H HO OH O O O + H 2 O 3. Show how you would do the following transformation. The twist is every cyclohexane has to be converted to product. O O OH
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4. Please show how you would make the mono-deuterio benzylic alcohol from methyl benzyl ester. O O OH D H 5. Show how you would do the following reaction. The twist here is that every carbon of the ester has to be converted to the 1,1-didutereoethanol.
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Unformatted text preview: O O OH D D 6. Show how to do the following transformation. OH O 7. Show how to do the following transformation. Methanol is your only carbon source. CH 3 OH O O 8. Show the detailed mechanism for the ester formation steps in the last problem. OH O + OH H O O + H 2 O 9. Show a detailed mechanism for this transesterification. O O + OH H O O + OH 10. Sapontify (hydrolyze in basic conditions) the ester formed in the last problem. O O H 2 O/OH OH O + OH 11. Show how you would perform the following chemical transformation. OH O...
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This note was uploaded on 09/25/2009 for the course CH 223 taught by Professor Brown during the Summer '08 term at N.C. State.

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More Practice Synthesis Problems - O O OH D D 6. Show how...

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