Help with this question please......draw if poss Fill in the Blank.1. Complete the following synthetic schemes by filling in the boxes with the appropriate reagent(s),starting material(s) or predominant product(s). If a racemic mixture is formed; draw oneenantiomer and write (+/-) next to the structure. If you do not think a reaction will take place, write"No Reaction". If no reagents will promote the transformation, write "No Reagents".OHNHBox 3OHPyridineNH3Box 2(2 equiv.)Box 11)Cat. H3O+H₂OH₂OHCI (1 equiv.)HeatBox 42. H₂O work-upBox 5MgBr(2 equiv.)2) H₂OBox 6Box 7Box 8

Step 1:Box 1: The reactant is an acid chloride, while the product is a carboxylic acid. The acid…

Answered: Fill in the Blank. 1. Complete the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter11: Addition To Alkynes

Section: Chapter Questions

Problem 11CTQ

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The question is: "Draw the curved arrow mechanism for the reaction between pentan-2-one and (CH3)3O– in t-butanol to form an enolate. Draw all electrons and charges on both resonance structures. Then answer the question about the reaction." I got the initial arrows correct, but am not entirely sure what the carbanion intermediate would look like and then what the curved arrows would be to convert it to its final oxanion form
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I'm having hard time finding the missing reagent. Can you elaborate the transformation and is there more than one synthetic step?
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