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- Draw the major organic products for each of the following reactions. If no reaction occurs, state so. (a) Br (b) ? + (CH),CuLi → ? + CuLi (c) (d) Br CI. CuLi ? ? + CuLi 2 +2. Give the structure for the following compounds.Question 8 Identify the type of isomer for (5)-3-methylheptane. O Racemic (*) O Levorotatory isomer (-) O Dextrorotatory isomer (+) O Has to be experimentally determined
- Draw the structure of the expected organic product(s) formed in the following reactions including correct sine echemistry. If the product is racemic write racemic or draw both isomers. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state "No Reaction".Question 8 Identify the type of isomer for (R)-3-bromoheptane. O Has to be experimentally determined O Dextrorotatory isomer (+) O Levorotatory isomer (-) Racemic (*)Reaction of (CH3)3CH with Cl2 forms two products: (CH3)2CHCH2Cl (63%) and (CH3)3CCl (37%). Why is the major product formed by cleavage of the stronger 1° C–H bond?
- Write the structure of the organic product in each of the following reactions. If electrophilic aromatic substitution occurs assume only monosubustitution.Compare and contrast the physical and chemical properties of: • propan-1-ol and propan-2-ol; • (E)-butenedioic acid (fumaric acid) and (Z)-butenedoic acid (maleic acid)Draw all the geometric isomers for 3-bromo-2-chloropent-2-ene Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charges), A Ⓡ H2EXP CONT?