whats the mechanism? if possible, please explain the steps intramolecular Aldol о оне Сиз
B. Bonus (10 pts) Intramolecular Aldol.. о он. CH3
Draw the mechanism and product for the Intramolecular Aldol condensation. Assume added at the end of the reaction
10 Question (3 points) @ See page 920 Complete the mechanism for the intramolecular aldol reaction shown below. Add the missing curved arrow notation, lone pair electrons, and nonzero formal charges to all boxes. The reaction requires a base (e.g., NaOH) but we will ignore the Nat because it does not participate in the mechanism. Do not add any other reagents. :0— I Elcb Draw lone pairs, non-zero formal charges, and curved arrows to show how hydroxide reacts with the...
draw a mechanism each steps, and explain stereochemistry for
product
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2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale. Answer:
2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale. Answer:
2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale. Answer:
2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale. Answer:
2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale. Answer:
please answer all of the 4 questions
What cyclic product is formed in the intramolecular Aldol condensation when the following compound is treated with aqueous NaOH? OT 11 0 0 IV What is the Aldol addition product formed from reaction of the following compound with itself? ++,C#o Cาถวาย 0 0 0 What is the cyclic product formed in the intramolecular Aldol condensation when the following compound is treated with aqueous NaOH? 08 pod od IV OT O II III O...