58 722
Assignments Done
Successfully Done
In March 2018
Your physics homework can be a real challenge, and the due date can be really close — feel free to use our assistance and get the desired result.
Be sure that math assignments completed by our experts will be error-free and done according to your instructions specified in the submitted order form.
Our experts will gladly share their knowledge and help you with programming homework. Keep up with the world’s newest programming trends.

Answer on Organic Chemistry Question for anissa

Question #23154
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
Expert's answer
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.

Need a fast expert's response?

Submit order

and get a quick answer at the best price

for any assignment or question with DETAILED EXPLANATIONS!


No comments. Be first!

Leave a comment

Ask Your question