4. Draw all of the C,HaCha l of the CH12Cl2 products (including different stereoisomers) formed during the chlorination of (18)-1-chloro-3,4-dimethylcyclopentane. Number each different structure (1, 2, 3, etc).
5./ Design a multistep synthesis to make benzyl butanoate (shown below) from propane, acetylene, benzyl bromide and any other reagents Br Ph
6. When the following two molecules undergo a Diels-Alder reaction, only one product is formed. Draw the structure of the product and explain (using words and resonance structures) why only 1 product is formed.
& Draw a step-by-step mechanism for the following transformation. он он 1) NaNH2 13 2) H20
Show transcribed image text4. Draw all of the C,HaCha l of the CH12Cl2 products (including different stereoisomers) formed during the chlorination of (18)-1-chloro-3,4-dimethylcyclopentane. Number each different structure (1, 2, 3, etc). 5./ Design a multistep synthesis to make benzyl butanoate (shown below) from propane, acetylene, benzyl bromide and any other reagents Br Ph 6. When the following two molecules undergo a Diels-Alder reaction, only one product is formed. Draw the structure of the product and explain (using words and resonance structures) why only 1 product is formed. & Draw a step-by-step mechanism for the following transformation. он он 1) NaNH2 13 2) H20
