can you please draw out the mechanisms for the following two transformations, using both intra molecular aldol and a retro ladol reactions. Thank you! B 叻 HO Na OEt ethanol оф OH
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- Draw the product of the following reaction; include the mechanism (using arrows etc.)-Methylbutanal undergoes an aldol reaction to form 3-hydroxy-2-isopropyl-5-methylhexanal. Additional heating in base will form the aldol dehydration product. 10% NCH 5°C Step 1: add curved arrows. Select Draw Templates Mar |||||||||||| M Complete the mechanism for the dehydration reaction by adding missing honds and curved arrows. Draw the aldol dehydration product in the last step. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the tructure, use the undo button in the lower-left corner of the panel to reset the structure 3 Ć НО Era Q2Q Step 3: complete the structure of the product. Select Draw Templates Mar XTZ ? 10-1 Q2Q Step 2: complete the structure and add curved arrows. Select Draw Templates More ||||||| Era AND heat2 CH3COOCH,CH3 C2H5O'K*/C2H5OH ---> CH3COCH,COOCH,CH3 [+] Hofmann elimination Clemmensen reduction Claisen condensation O Cannizzaro reaction O Aldol condensation
- Draw the complete mechanism for the acetal formation.Show how to prepare a,b-unsaturated ketone by an aldol reaction followed by dehydration of the aldol product.The mechanism for the following reaction involves bromination addition followed by a nucleophilic attack. Draw the complete mechanism for the reaction.