could you please help me with this;
the reductive ozonolysis of 1-methyl cyclohexene conduct to a compound A. This compound treated in basic environment leads to a cyclization reaction following a specific carbonyl compounds. Give feedback and clarify the mechanisms of the products likely to form.
thank you
1
Expert's answer
2013-01-31T08:34:36-0500
Methylcyclohexane is a fully saturated strainless hydrocarbon and will not undergo a reaction with ozone, except at high concentrations (under such conditions it combusts). If you meant, 1-methylcyclohexene, the product is obtained by removing the double bond and attaching a double-bonded oxygen to each carbon atom. This gives 6-oxoheptanal. Then, after reducing you'll get 6-oxoheptanoic acid. This is your compound A. The last one specific carbonyl compound is 2-methylcyclohexanone.
Numbers and figures are an essential part of our world, necessary for almost everything we do every day. As important…
APPROVED BY CLIENTS
"assignmentexpert.com" is professional group of people in Math subjects! They did assignments in very high level of mathematical modelling in the best quality. Thanks a lot
Comments
Leave a comment