This is another synthesis problem. Show reagents and intermediates synthesized along the way that allow you to produce the product from the given starting material. For this one do NOT assume you can isolate isomers - meaning - the product isomers shown must be the only predominant isomers you make during your synthesis! ? CH3OH
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- Each of these reaction produces ONE MAJOR PRODUCT. In each case, draw this product in the box provided, including appropriate stereochemistry when applicable. For multi-step reactions, just give the FINAL product, no intermediates.In the presence of light or heat, diazomethane (CH,N2) creates a carbene, which then adds to an alkene to make a cyclopropane. In the boxes below. draw the mechanism arrows for the reaction. H INEN: INE N:Show how you would synthesize each of the following syntheses (more than one step may be required)
- Br Brz CH3 CH3 H3C CH2CI2 H3C Br 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 CH,Cl). 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: :Br: .CH3 H3C H3C CH3 Br:Draw mechanisms and products for ONLY THE THIRD ROW of reagents with each combination of alkene if possiblePropose a complete mechanism to account for the two products of the reaction shown below. Please illustrate any and all intermediates, resonance forms, curved arrows, formal charges, and lone pairs as necessary. CI OCH2CH3 Br HCI Br + Br CH;CH2OH
- U U U CI Recall that the Friedel-Crafts alkylation reaction forms a new C-C bond between an aromatic ring and an alkyl halide, in the presence of an appropriate Lewis Acid. Which of the following (one or more than one) DO work well in Friedel-Crafts alkylation reactions? OH CI +a NO2 CI as the alkyl halide for the reactionProvide the structure(s) of the expected major organic product of the reaction shown. 1) Disiamylborane 2) H₂O₂, NaOH OI O II ||| O IV OV CH3CH₂C(CH3)2C=CH OH OH xx xo IVI would like to understand how to mechanism of this reactions occur
- For the following reaction there are three (3) possible products. Two of the products are expected to be minor and one product is expected to be a major product. Br H₂O Name and draw out the step-by-step mechanisms by which each of the products is formed. Briefly explain why one of the three products is expected to be a major product.Please answer the following questions in detail (show all the steps)Please answer BOTH questions, thanks so much!