5. Draw each reaction entirely using line structures and follow the instructions below. Give the structures of compounds A through D in the following series of equations. NINH, NH HBr, heat A C B+D B CH₂CH₂CH₂C=CC(CH₂),

Compound A is an aromatic compound with the molecular formula C8H8. When treated with excess BR2, compound A is converted into compound B, with the molecular formula C8H8BR2. Draw the structure of compound a. 

20:33 1 : ●●● all the proper notations for depicting resonance. 4. Provide the full mechanism (curved arrows and intermediates) that leads to the product in the scheme below. Draw the structure of the product to help you see how the starting materials will combine. Use that as a clue to figure out how to draw the mechanism arrows. ccare in your scheme. Be sure to use NaOEt 00 i 5. Provide the major organic product of the reaction shown. Determine if these conditions are best for SN2, SN1, E2, or E1. Be sure to indicate stereochemistry by using the proper wedges/dashes in the product. acetone phenyl butanoate Send a chat O

Hw.215.

If pentane-1,3-diol reacts with in the presence of pyridine it gives product A. And if A reacts with in the presence of pyridine it gives a product B. Indicate which products A and B are.

Give detailed Solution with explanation needed