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- Fill in the missing intermediates(two), regents(two), and the fill product in the following multi-step synthesis. Assume all reactions proceed too quickly for rearrangements to take placeConsider the given reaction in which NC−NC− is the nucleophile and CH3CNCH3CN is the solvent. The reactant molecule has a structure with solid and dashed wedge bonds. A solid wedge () is used to show the bond that is above the plane of the paper, and a dashed wedge () is used to show the bond that is behind the plane of the paper. Draw the product of the following reaction:#16f. Provide the missing reactants, reagents, or products for the following reaction sequences below.
- Please provide the reagents, reactants, and/or the products for the following reactions.H3C CH3 H3C NA C→XT Br Br₂ CH₂Cl₂ H3C Electrophilic addition of bromine, Br₂, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH₂Cl₂. CH3 Br In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br CH3 H3C CH37. Identify the correct reaction conditions for the following conversion? CH, CH;CHCH;C=N CH, HOʻHD³HDHDD-