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- Hi, I was wondering if I could get help to understand this question? I have the starting product and then have to get an actual product and I'm not sure if I'm doing this right or why the product is supposed to be a different product because I understand how the mechanism gets to the desired product.#16d. Provide the missing reactants, reagents, or products for the following reaction sequences below.Can you give me the reaction mechanism for this reaction?
- Organic Chemistry 2: Draw the mechanism for the following reaction: OHC. 3 EtONa EtOH Ćstep-by-step mechanism for the following reaction4. A CHEM 245 student wants to synthesize some ethylene glycol to use as antifreeze in his radiator this winter. He proposes the following reaction to his instructor, who quickly explains that this reaction won't work as proposed due to the student's choice of reagent. 1) NaH 2) H20 OH Но a) Why can't sodium hydride (NaH) be used as the nucleophile in the reaction above? b) Propose an alternate reagent that COULD be used with the ethylene oxide to successfully give the desired ethylene glycol product.
- Write the reaction mechanism for the reaction on the image and show the main organic product. Please include all of the steps in the explanation.Answer the question below the reaction. O4S H3C H3C H3C OH In the first step of the reaction mechanism, which of the following is formed? CH3 H3C CH3 CH3 + Excess NH4Cl OH CH3 (+) -OH2 CH 3 CH3 OH CH3 H₂SO₁ CH3 CI ха +H2OIdentify the product for this reaction. c N /Rd,C 1am/25°C OH
- H Br Br2 CH2Cl2 H, Br Electrophilic addition of bromine, Brɔ, 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 CH2Clɔ. 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 H Br H- Br H. :Br: Proviouc NoxtSelect the correct product for the following reaction.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.
