1. Draw all possible products of the reactions below. Circle the major product(s). Include stereochemistry in your answers. For best practice, draw all the mechanisms! KCN Br H₂O NaOEt NaOMe
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- Predict the product of the reaction shown and complete the curved-arrow mechanism for its formation. (Hint: Friedal- Crafts alkylations can be used to form rings.) AICI, → a compound C,H2 + HCI PHCH,CH,CH,CH,CI- Step 1: Draw one curved arrow. Step 2: Complete the structure, then draw curved arrows for the EAS reaction. Select Draw Rings More Erase Select DrawRings More Erase H Al Cl H Al Cl : C : Al : d :Help please!What's the product of an HOT-induced E2 reaction of the R,S dibromide? Br Ph Br Ph KOH A Again, remember that the alignment of the Br and H will determine the stereochemistry. O O O Ph Ph Br. Ph Ph Ph Br Ph Br Ph Br Ph
- Draw the structures (using Chem Draw) of the final products for each of the following dihydroxylation reactions (A-D) outlined in a and b below. a. Be sure show ALL possible stereoisomers. Use planar structure only, no chairs! b. Also indicate if there is more than one stereoisomer, indicate the relationship between the isomers (identical, enantiomers, or diastereomers). A KMnO4 B 1. oxone acetone 2. H3O+/H₂O KMnO4 D 1. oxone acetone 2. H3O+/H₂O4. Draw the mechanism of the reaction shown below. HO H3PO4See image below