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- Give the minor product of the following reaction. CO,Me heat CO,Me CO,Me cO, Me cO, Me co, Me H. Meo, co,Me There is no reaction under these conditions or the correct product is not listed here.3. Give the mechanism(s) and product(s) for the reaction below. Show stereochemistry. H D H L CH3 D CH3 H₂O₂, HCI hvProvide the product and mechanism for the reaction: ОН Cro, H,SO, H,0
- Draw the organic product of the reaction below. Show stereochemistry when relevant. If the product exists as a pair of enantiomers, draw only one. + 1. LIAIH 4 2. H₂O T X Ś Ć Click and drag to start drawing a structure.Draw structural formulas for the major organic product(s) of the reaction shown below. CN AICI3 + (CH3)2CHCI • You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. Remember to include all of the formal charges on the atoms of any nitro groups.4. Write a mechanism to account for the product formed in each of the following reactions. Use arrows to show electron flow and include the structure of all reaction intermediates CHCH.CCH₂ B₂ CH,COOH 9 CH,CHCCH Br 00/th HB
- Draw the structural formula of the product of the reaction shown below. H₂SO4 O + H₂O • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, just draw one stereoisomer. *4 Sn [F ? ChemDoodleDraw a structural formula for the substitution product of the reaction shown below. H/ ● (CH3)3C |YY Br ΔΟ H Na • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one stereoisomer of product is formed, draw both. Separate multiple products using the + sign from the drop-down menu. • Products that are initially formed as ions should be drawn in their neutral forms. SH acetone [F5) Provide the expected mechanism for the following reaction. Please show all intermediates and use arrows to show the movement of electrons (you do not have to show transition states). (1 pt) ii CI NaOH (2 equiv)
- Bicyclo-2,5-heptadiene can be prepared in two steps from cyclopentadiene and vinyl chloride. Provide a mechanism for each step.When 2-pentene is treated with Cl2 in methanol, three products are formed. Account for the formation of each product (you need not explain their relative percentages).4. Propose a structure(s) for the product(s) of the following reactions. O2N. HO NaH