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- Pleas explain how this process occurs. Identify SN1, SN2, E2, E1, nucleophiles and electrophiles.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.For the following reaction, indicate the major product. Be sure to indicate stereochemistry when relevant
- Under acid-catalyzed conditions, epoxides can be opened by a variety of nucleophiles other than water, such as alcohols. In such a case, the nucleophile will generally attack at the more substituted position. Using this information, predict the products for each of the following reactions (a-b): ? 1) RCO-H 2) [H₂SOJ Modify the given structure to draw the major product(s). Use the single bond tool to interconvert between double and single bonds. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. CH₂ Edit Drawing AWrite the complete stepwise mechanism for each of the following reactions. Show all electronflow with arrows and draw all intermediate structures.Draw out a complete arrow-pushing mechanism for the following reaction. This reaction is explicitly done with heat. O NaOH, H₂O heat
- Each of these reactions 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.Given the following reaction sequence, determine the structures of A and B, including proper stereochemistry. Br NaOH A DMSO 1. CH3(CH)3Li В 1. NaH 2. CI- Br 2.Complete the following reactions: indicate the mechanism (SN1 or SN2). If the reaction does not proceed, indicate so and the reason as to why it would not.
