please help 10. Draw the major product for bromination of each diene below. The products are...
NBS bromination of cyclohexa-1,4-diene yields 2 products. Draw them.Do not consider stereochemistry.I know cyclohexa-1,4-diene looks like this but idk how to do it!
5. a) Draw the major 1,2-addition product and the major 1,4-addition product of each of the following reactions. Label each product as either the 1,2-addition product or 1,4-addition product and as either the thermodynamic or kinetic product. (12 pts) H" catalyst H catalyst b) Consider the reaction of a nucleophile with conjugated carbonyl. Provide an example of a nucleophile that would favor the 1,2-addition product and explain why. Provide an example of a nucleophile that would favor the 1,4-addition product...
When 1,4-dimethylcyclohepta-1,3-diene is treated with HBr at an elevated temperature, the 1,2 product predominates rather than the 1,4 adduct. Explain and draw the 1,2 and 1,4 products.
help Thank you 4. (10 pts) Draw all possible products for the following reaction including stereoisomers. Note that the addition occurs through a "syn" mechanism. Is the product solution optically active (yes or no)? 1. BAHATHF 2. NaOH, HO (8 pts) Provide a complete mechanism for the reaction below and include lone-pairs of electrons and formal charges. Show all products formed including stereoisomers. Is the product solution optically active (yes or no)? Bras 11. (8 pts) Draw all four regiochemical...
Mono addition of HCl to unsymmetrical dienes generally produces four products - two 1,2-addition products and two 1,4-addition products. In some cases, such as the following, a 1,2-addition product and a 1,4-addition product may have the same structure, and thus only three distinct products are formed. Draw the reactant diene that forms the following three products, and identify the addition route that forms each product.
Answer the following questions about radical halogenation QUESTION 1 Performing allylic bromination of an asymmetric alkene produces two regiochemical outcomes due to resonance, and two conformations (R) and (S) for each chirality center produced. This is further complicated if you make the mistake of using Br2 as your source of bromine radicals, as the addition reaction producing alkyl dibromides competes with the allylic bromination. Br2, hv ??? Categorize each of the compounds shown below as an [A] allylic bromination product,...
For each addition route of the reaction, draw the structure(s) of the major product(s), including stereochemistry. 1,2-addition: y 1,4-addition:
Alder Re? 9. Draw the two major products for the following reaction. a. Identify each as either a 1,2 or 1,4 addition product. b. Write either "thermodynamic" or "kinetic" underneath each one. c. Draw the two resonance structures for the intermediate from which both form H-Br ton nroducts for the following reaction. Draw the the major product or products for the following reaction. Drow the resonance structures for the intermediate from which both form Bra/ hv NBS/ peroxides 11. Give...
Draw the major product you'd expect from the radical bromination of 2,2,4-trimethylpentane. O % 0 Draw all possible monochlorinated products you'd expect upon treating 2-methylbutane with Chand irradiated with UV light
Draw the two major products obtained in the reaction shown.Draw the major 1,2- and 1,4-addition products obtained in the reaction shown. Assume that both are derived from the most stable carbocation intermediate.