a. multi-step reaction

provide full an detailed reaction mechanism given the following reactants, products, and conditions

Give correct detailed mechanism Solution with explanation needed.   Don't give Handwritten answer

Give the mechanistic Symbols CE1, E₂, SN, SN²) that are Con Sistent with Statemenst! most each of the following O Methyl halides react with Sodium ethoxide in eth and only by this mechanism In ethanol that contains Sodiumn ethoxide, tert-butyl bromide reacts mainly by this mechanism c) these reaction Con certed DJ these involve are mechanisms infere processes reactions mechanisms carbc cation intermedites E) Reactions proceeding by mechanisms are these Sterospecific

Mechanism time! Upon treating the indicated starting material with HCl the resultant polycyclic product was formed. Please provide a reasonable arrow-pushing mechanism to account for the formation of the indicated product, including the drawing of all resonance structures after the requisite C-C bond has bond.

Please answer the questions below asap. If you need to go through the concept, please do so   Concept link:  https://drive.google.com/file/d/1AxC3YQgssDWnFFnH4xWsV51GiltLulRw/view?usp=sharing   Questions:

Suggest how you would synthesize each compound, PLEASE use cyclopentanONE (with a ketone present!!) as one of the reagents!

Please don't provide handwritten solution ....

3. Predict the major product for the reaction shown here and draw the complete detailed mechanism for each reaction. Explain your answers. Provide which product is the thermodynamic and kinetic product. O: e 1. LDA 2. CI CHE 1. NaOC(CH3)3 2. CI

provide the mechanism! The tautomer that predominates in aqueous solution A. Enol B. Keto form