Provide a detailed mechanism (with mechanism step PT, LLG, CR, NA) to demonstrate the final product. Each curved arrow = +1, each labeled step name = +1. H+ ру
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- draw and explain the mechanism of this reaction OH CH₂ PhCOCI in py CH3 KOH in py 3 C OH H₂SO, in 0000 CH, CON5. a) When the molecule below is treated with HCI, the product distribution shown is obtained. Use curved arrow formalism to draw a mechanism for this process. Account for the product distribution and draw resonance structures for the intermediate that leads to the major product. The m HCI CI + s 1o(29nil no awa eib ys leldwsio (2tniog 01).E (15 % CI2 tw ledsl< 1% lad olualom 85 %Predict the product(s) and provide the complete mechanism for each reaction below.
- Please help with explanation need.8А. Draw a reasonable mechanism for the following reaction, with clear indication of stereochemistry. HO Br2 BrDescribe the detailed mechanism of the given reaction. Also, suggest the regioselectivity of the product formed. Also, S 8 Describe the detailed mechanism of the given reaction. Also, suggest the regioselectivity of the product formed. MeO- Cat.; NaOH DMSO Cat.: OMe
- Mechanism: Show a detailed reaction mechanism for the following reaction. Include the structure of the expected products and appropriate stereochemistry for all steps. Assume all reagents are in excess.*Provide the product(s) of each reaction below. Label each product with the reaction mechanism that produced it (SN2/SN1/E1/E2) and point out major vs. minor elimination products. Pay attention to stereochemistry as appropriate. Br H;CO. ONa CI Nao b) CF3 Ph Br CD,OH c) Ph7/ Give the products of each of the following reactions: 1- 1- CH3Mgbr ? 2- H20 Me 2- + CH3OH -→ OCH3 HCI 3- ? H2O NO2 ? + ? NO2 4- CH3CH2 =0+ H2NNH 1- LIAIH4 5- 2- H20 Me NHME HCI + C2H$OH + ? + ? 8/ Propose a mechanism for each of the following : 1- CH3 - C - NHCH3 + LIAIH4 → an amine an amide NH2 NH2 2- Me H2O 3- R- C N: R-C -OH