The target compound that you should synthesize is bicyclo[2.2.1]hept-5-ene-2-carboxyl ic acid methyl ester. This is a cycloaddition reaction. Examine the product to determine the reactive partners. Keep in mind the position of the alkene in the product. Try pushing the electrons backwards to reveal the needed substrates. Keep in mind the stereochemistry of the process. Required:
a. List the starting materials, solvent, reagent, and products formed.
b. How long did it take to finish the reaction?
c. What are the TLC values (R,) for

1. Starting Materials
2. Products

c. Write a mechanism for this reaction. (you may draw the

explanation:

two years ago, when picking flowers in the mountains back of yosemite valley, i found a book. it was blotted and storm-beaten; all of its outer pages were mealy and crumbly. the paper seemed to dissolve like the snow beneath which it had been buried, however; many of the inner pages were well preserved. and although all were more or less stained and torn, whole chapters were easily readable. this is the condition of the great open book of yosemite glaciers today; its granite pages have been torn and blurred by the same storms that wasted the castaway book.

two years ago, when picking flowers in the mountains back of yosemite valley; i found a book. it was blotted and storm-beaten, all of its outer pages were mealy and crumbly. the paper seemed to dissolve like the snow beneath which it had been buried, however, many of the inner pages were well preserved. and although all were more or less stained and torn; whole chapters were easily readable. this is the condition of the great open book of yosemite glaciers today, its granite pages have been torn and blurred by the same storms that wasted the castaway book.

i believe it is c for plato

they were both partners

explanation:

doesnt need to be one