help with both parts and step by step mechanism (iv) Provide a detailed mechanism for the Claisen condensation reaction between L and M, andgive the structure of product N. In your answer, indicate which step is responsible for drivingthe reaction to completion.MeOOL+AMeOMOMe(v) Identify reactant O required to react with ketone A in order to form a,ß-unsaturated ketone P.Explain the type of reaction taking place and draw the intermediate that under the reactionconditions undergoes formation of P (mechanisms not required).NaOH(aq)(1) NaOMereflux(2) acidicwork-upMeONP

iv) Claisen condensation reaction: The coupling reaction which results a beta-keto ester or a…

(iv) Provide a detailed mechanism for the Claisen condensation reaction between L and M, and give the structure of product N. In your answer, indicate which step is responsible for driving the reaction to completion. MeO + A MeO OMe M NaOH(aq) (1) NaOMe (v) Identify reactant O required to react with ketone A in order to form a,ß-unsaturated ketone P. Explain the type of reaction taking place and draw the intermediate that under the reaction conditions undergoes formation of P (mechanisms not required). reflux (2) acidic work-up MeO N P

(iv) Provide a detailed mechanism for the Claisen condensation reaction between L and M, and give the structure of product N. In your answer, indicate which step is responsible for driving the reaction to completion. MeO + A MeO OMe M NaOH(aq) (1) NaOMe (v) Identify reactant O required to react with ketone A in order to form a,ß-unsaturated ketone P. Explain the type of reaction taking place and draw the intermediate that under the reaction conditions undergoes formation of P (mechanisms not required). reflux (2) acidic work-up MeO N P

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 20MP

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(iv) Provide a detailed mechanism for the Claisen condensation reaction between L and M, and give the structure of product N. In your answer, indicate which step is responsible for driving the reaction to completion. MeO O L + A MeO M OMe (v) Identify reactant O required to react with ketone A in order to form a,ß-unsaturated ketone P. Explain the type of reaction taking place and draw the intermediate that under the reaction conditions undergoes formation of P (mechanisms not required). NaOH(aq) (1) NaOMe reflux (2) acidic work-up MeO N P
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