Ozonolysis of propene followed by reduction with zinc and acetic acid
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MECHANISM FOR REACTION OF ALKENE OZONOLYSISStep 1:
The π electrons act as the nucleophile, attacking the ozone at the electrophilic terminal O. A second C-O is formed by the nucleophilic O attacking the other end of the C=C.Step 2:
The cyclic species called the malozonide rearranges to the ozonide. Step 3:
The ozonide decomposes on work-up. Reductive work-up with (usually Zn / acetic acid) gives the two carbonyl groups.
The π electrons act as the nucleophile, attacking the ozone at the electrophilic terminal O. A second C-O is formed by the nucleophilic O attacking the other end of the C=C.Step 2:
The cyclic species called the malozonide rearranges to the ozonide. Step 3:
The ozonide decomposes on work-up. Reductive work-up with (usually Zn / acetic acid) gives the two carbonyl groups.
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