Organic Chemistry
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What product would form in the following reaction of an ester?
Rationalize why the carbonyl oxygen of the ester attacks the aluminum of DIBAL-H instead of the alkoxy oxygen in the following reaction.
What major product is expected from the given reaction?
Show how the following conversion can be achieved with good yield. Use any necessary reagents.
Show how 1-bromopentane can be converted to hexanal. Provide any necessary reagents.
(i) Predict the main product obtained when the molecule below reacts with DIBAl-H.
(ii) Based on your answer, is there a need to convert the ester to another ester to accomplish what DIBAl-H is intended to do?
What is the anticipated product of the reaction between 2-cyclopentylacetonitrile and DIBAL, followed by hydrolysis?
Draw the structures of the products formed by the reactions below: