For the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. + X 52 NaOH Cli da
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- 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. Ö Br □ + X NaOH SFor the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. + NaOH Click and drag to start drawing a structure.the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. NaOH
- Draw the major product of this reaction. Ignore inorganic byproducts. 1. CrO3, H2SO4 2. Neutralizing work-up Select to Draw HDraw the major product of this reaction. Ignore inorganic byproducts. 0 1. CrO3, H₂SO4 2. Neutralizing work-up H .For the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. Cl + + X Na OH Click and drag to start drawing a structure.
- 3. Perform the following tasks for each reaction. i. Identify the functional group (FG) in the starting material with the most accurate name: alcohol, aldehyde, epoxide, ester, ether, or halohydrin. ii. Label the reagent over the arrow as a good nucleophile; a strong base; and/or a strong acid. (A reagent can have more than one label.) Draw the major organic product. (Hint: Remember to keep track of stereochemistry over the course of the reaction if given. It may be helpful to redraw the starting material in the conformation needed to close epoxide ring.) ii. iii. Product i. Starting Material OH ii. Reagent a. D. NaOH FG = b. Excess HBr FG = с. 1. Li(CH2);CH3 2. H3O* (Acidic workup for neutralizing charge) FG = d. ОН NaH FG = е. HBr FG =This reaction is an example of conjugate addition of a nucleophile to an a,ẞ-unsaturated carbonyl. H3C LOCH3 H₂O H3C OCH3 OCH3 Draw the two resonance structures of the enolate anion intermediate for this reaction. • Draw an R1 group in place of CoA. The R group tool is located in the charges and lone pairs drop-down menu. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. • O H CH3 ? [F1. Draw the starting structure that would lead to this major product 2. Draw the major product of this reaction. Ignore inorganic 3. Draw the major product of this reaction. Ignore inorganic under these conditions. byproducts. byproducts. H3O* H3O* H3O* НО
- 29) Draw all of the expected products for the following reaction. Circle the most dominant product in each reaction. 'BUOK 3 NaOEt1. Propose a synthetic route from the starting material to the product. Show each individual reaction step and all intermediate products. Assume acidic workups occur if needed. Starting Material Product a. b. Hint: Number the carbons in your starting material and your product. Starting Material Product a-an c. Hint: Pay attention to stereochemistry. Starting Material Product 41. Show a detailed mechanism for the following reaction. 1. Cl2, NaOH HO. 2. H3O* 1