different reactions with specific conditions given (i.e., reagent and solvent). -Please include reactions that include the following functional groups at some point in the planed synthesis: an alkene, an ether, an alcohol, and an alkylhalide. Can include other functional groups, but these are the minimum. -Must make at least one C-C bond in the synthetic route. - Please include detailed arrow pushing mechanisms for each proposed step.

The reaction shown here is an example of the Corey- 1. CH3I 2. NaH HN-CH2 Chaykovsky aziridination reaction. Draw its complete, detailed mechanism. Hint: See Problem 17.57. H3C CH3 3. NH R' .C. R' R

Predict the product of this E2 elimination reaction. ||| Brill.... H3C Ph Ph H3C Ph Ph Ph CH3 || reaction H3C Ph IV CH3 NaOCH3 Ph H3C Bril... Ph CH3 Ph CH₂ Ph

Draw th jor substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. ***** Camil С HO :0 + X Click and drag to start drawing a structure. E ak 15

Draw a valid and complete reaction mechanism for one (and only one) of the following reactions J, K, or L. Be sure to include any and all stereochemistry throughout the reaction mechanism. Include all appropriate steps, arrows, and electrons involved. Draw all of the intermediates (and/or transition states where discussed in lecture), and label all non-zero formal charges. For your reaction, also be certain draw the starting material, the reactant(s), and all possible products. Please label these as "major" and "minor" (and "very minor," if needed). You may use a label more than once, but each structure should only have one label. Reaction J OH H,SO4, A Reaction K 1. PB13, 2. NaCN OH Reaction L HI, A

I really need help

Pls help ASAP on both pls I HUMBLY request

No need explanation..give clear solution..with reaction mechanism..give answer asap

tu please don't provide handwritten solution

4. Provide the complete mechanism using Curved Arrow Formalism for the compound shown below treated with H2SO4/H2O. Include all resonance stabilized intermediates. Tell which layer (aqueous or organic) the product(s) will be isolated in. HO. N.