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2 cards from this section. Quick, good the night before a test.
What is the main product when an alkene undergoes acid-catalyzed hydration?
Think about the functional group formed.
What type of alcohol results from the reduction of an aldehyde?
See if you remember the difference between aldehydes and ketones.
What rule governs the addition of H2O to unsymmetrical alkenes?
This determines where the hydrogen goes during addition.
True or False: Hydroboration adds boron to the less substituted carbon atom.
Remember, it goes against Markovnikov’s rule.
Explain the mechanism of the reduction of a ketone using sodium borohydride.
Visualize how the carbonyl is transformed.
Design a synthetic route to prepare a specific alcohol from an alkene of your choice. Include all necessary reagents.
Think about which methods align with your desired starting material.
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