1. An oxetane is a four-membered ring ether (shown on the right), and it can also be opened via nucleophilic attack under neutral or basic conditions. (a) Would you expect an oxetane to be more or less reactive than an epoxide? CONCISELY explain. (b) How would you carry out the following synthesis to prepare the target molecule? CH3 ??? HO Target molecule oxetane
1. An oxetane is a four-membered ring ether (shown on the right), and it can also be opened via nucleophilic attack under neutral or basic conditions. (a) Would you expect an oxetane to be more or less reactive than an epoxide? CONCISELY explain. (b) How would you carry out the following synthesis to prepare the target molecule? CH3 ??? HO Target molecule oxetane
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
Transcribed Image Text:1. An oxetane is a four-membered ring ether (shown on the right), and it can also be
opened via nucleophilic attack under neutral or basic conditions.
(a) Would you expect an oxetane to be more or less reactive than an epoxide?
CONCISELY explain.
(b) How would you carry out the following synthesis to prepare the target molecule?
CH3
???
HO
Target molecule
oxetane
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