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Step by step
Solved in 2 steps
- Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from the given starting material (on the right). (any reagents maybe usedChoose the reagent that would be most likely to complete this reaction.I’m having trouble find the major product could you help find the reagent that is reasonable to find the product?
- Out of the minor product which one would be correct? The one you drew isn't shownThe pKa of our product is ~ 2-3 units lower than the pKa of phenol. Draw all possible resonance structures of the conjugate base of the product, and use these to explain why our product is so much more acidic than phenol.GIVE THE COMPLETE PRODUCT OF THE FOLLOWING REAGENTS.