2. Propose an efficient synthesis for each of the following transformations. Pay careful attention to both the regio and stereochemical outcomes. ¡ H H racemic
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- 3. Provide a reasonable synthesis for the following transformations. You may use any reactions that we have learned until this point. STEPS STEPSorganic chemistry please solve the followingIV. Provide the correct product resulting from the following transformation, and its proper mechanism. Mechanism HI
- Which of the folloqing best describes the major product for the following substitution reaction? (Only the major product of this reaction I will add as a photo!) Please show all steps for how you get to this for my full understanding!Give detailed Solution with explanationAddition proceeds preferentially through the most stable carbocation intermediate. At high temperature, 10-20 °C or higher, products equilibrate; and the most stable product predominates (thermodynamic control). At low temperature, 0 °C or lower, there is kinetic control of reaction products. CI CI b Write a mechanism for the first step of this reaction using curved arrows to show electron reorganization. Consult the arrow-pushing instructions for the convention on regiospecific electrophilic attack on a double bond. Arrow-pushing Instructions n →XT H-CI:
- Provide a mechanism including relevant resonance forms, intermediates, reaction arrows, and curved arrows showing electron flow.Please give a detailed stepwise mechanism for the following reactions of Q.1 and Q.2. All arrows, charges, intermediates, and resonance structures must be shown.React each molecule with each of the substrates on the right include step by step reaction also inclue arrows and draw