2. Draw the complete mechanism, using arrow-pushing, for the reaction of tert-butanol with bromide ion. Don't forget that this reaction is performed in acidic conditions (protonate the alcohol first).
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Solved in 3 steps with 1 images
- Draw the mechanism arrows for the acid-catalyzed hydrolysis of an acetal back to the aldehyde.Draw out the complete mechanism of the reaction and include all relevant electrons and arrows showing electron movement. NaOHa,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity.
- Come up with a reasonable mechanism for the following reactionDraw the mechanism of the following reaction (show the arrow pushing).Draw the major product for the oxidation reaction. Then, draw the proper FULL electron-pushing mechanism for the reaction, including ALL intermediates (with formal charges) and electron-pushing arrows. Label the electrophile and nucleophile in each step.