The reaction of the initiaior with the styrene m box as the major product rather than...
3. When 1-bromo-1-phenyl-ethane is heated in ethanolic potassium ethoxide, the major product is styrene. a. Write a detailed reaction scheme. b. Write a detailed mechanism using the standard conventions 4. When 2-bromo-1-phenylbutane is reacted in methanolic sodium methoxide, one might expect to see two products. However, only one product is formed to an appreciable extent, a. Write a detailed reaction scheme b. Write a detailed mechanism. c. Explain why only one of the possible products is formed to appreciable extent
M Draw the structure of the major organic product(s) of the reaction. M M OH HCI M sts pts M pts M • You do not have to consider stereochemistry • All carboxyl and amino groups should be drawn in the neutral form • If no reaction occurs, draw the organic starting material • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom • Separate multiple products using the + sign from the drop-down...
2. The following is a radical chain reaction. Br. heat a. Which product is the major product? (3 pts) b. Show two propagation steps for the formation of the major product. (6 pts) c. Explain, with intermediates, how the major product becomes the major. (6 pts) d. Explain, with TS, how the major product becomes the major. (6 pts)
write the major product and why a different product is obtained from part a. C. Write the major product for the following Reaction and explain why a di Product is obtained in this Reaction than was obtained in part a. Na (SHIOH write Following the major Reaction product for the Na C₂ HS OH
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...
Q 39 - (2 pts) Fill in the box with the major/predominant product(s) for the following reaction and indicate the stereochemistry where appropriate. NaOCH, CI *** no reaction will occur А В D с Q.40 - (2 pts) Fill in the box with the major/predominant product(s) for the following reaction and indicate the stereochemistry where appropriate. bhu no reaction will occur Ku D A B 941 - (2 pts) Which of the following is an intermediate when but-1-ene undergoes radical...
Attempts to isolate the product of this reaction yielded solid salicylic acid, rather than liquid wintergreen (methyl salicylate.) Why?
QUESTION 3 What is the structure of the major product for the following reaction? AgNO3 product(s) products) ethanol HOEL to go OOOOOO QUESTION 4 What is the major product for the following reaction? X Nal Nail product(s) products) acetone OET QUESTION 1 What is the structure of the major product for the following reaction? AgNO3 product(s) ethanol MOET HOET m oet ~ NO3 HOEL ~ NO HOE NO3 OOOOOO QUESTION 2 What is the structure of the major product for...
4. Reduction Mechanism. Draw the major product for the reduction reaction below in the box. Then, draw the proper FULL electron-pushing mechanism for the reaction, including ALL intermediates (with formal charges) and electron pushing arrows. Label the Electrophile and Nucleophile in each step! 1. NaBH4 2. H30+
4 pts What is the major organic product(s) of the following reaction? Name the product in the box (at least describe it) and upload a single file with all drawings for this quiz in the Module 5 File Upload assignment. EtMgBr - Paragraph