PLEASE HELP!!!!!
1) Given diene and dienophile reactants and final product of a multistep synthesis fill in the blank spots for the intermediate product and missing reagents to convert the intermediate to the final product of tertiary alcohol.
-Given diene and dienophile reactants and final product of a multistep synthesis fill in the blank spots for the intermediate product and missing reagents to convert the intermediate to the final product of tertiary alcohol.
2) Identify the most acidic proton on an odd number of carbon ring with only one sp3 atom such that all other atoms are connected to a pi bond. Which is the most acidic hydrogen? Why is this hydrogen acidic, what is the benefit of losing the H?
3) Identify which heteroatomic ring is aromatic. So you must recognize when lone pairs on a heteroatom are part of the pi system and know the following. If a heteroatom has 2 lone pairs, How many can be part of the pi network in an aromatic compound?
PLEASE HELP!!!!!
1) Given diene and dienophile reactants and final product of a multistep synthesis fill in the blank spots for the intermediate product and missing reagents to convert the intermediate to the final product of tertiary alcohol.
-Given diene and dienophile reactants and final product of a multistep synthesis fill in the blank spots for the intermediate product and missing reagents to convert the intermediate to the final product of tertiary alcohol.
2) Identify the most acidic proton on an odd number of carbon ring with only one sp3 atom such that all other atoms are connected to a pi bond. Which is the most acidic hydrogen? Why is this hydrogen acidic, what is the benefit of losing the H?
3) Identify which heteroatomic ring is aromatic. So you must recognize when lone pairs on a heteroatom are part of the pi system and know the following. If a heteroatom has 2 lone pairs, How many can be part of the pi network in an aromatic compound?
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