Propose a synthetic strategy for this reaction. Include all intermediate products.   Please don't provide handwriting solution

Devise a synthesis for benzophenone. You may only use benzene and formaldehyde as sources of carbon. You may use any other reagents necessary to carry out the transformations. typed solution

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please,complete those following reactions.

[Review Topics] [References] Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C CH3 H2O NaOH • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Nat, I', in your answer. • In cases where there is more than one answer, just draw one. C opy aste C. Previous Next Email Instructor Save and Ex Cengage Learning | Cengage Technical Support 5:48 PI 82°F 3/28/20

help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working

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Please provide only typed answer solution no handwritten solution needed allowed

Please help me with both these questions, i want to study today but I dont get this, please provide deep description while also making the answer clear

Suggest possible synthetic route for each of following transformations. Show the reagents, intermediates and products