Chapter 11: Q11-76E (page 350)
The reaction of 1-chlorooctane with CH3CO2 2 to give octyl acetate is greatly accelerated by adding a small quantity of iodide ion. Explain
Short Answer
Formation of the desired product
Chapter 11: Q11-76E (page 350)
The reaction of 1-chlorooctane with CH3CO2 2 to give octyl acetate is greatly accelerated by adding a small quantity of iodide ion. Explain
Formation of the desired product
All the tools & learning materials you need for study success - in one app.
Get started for freeHow might you prepare each of the following molecules using a nucleophilic substitution reaction at some step?
Which reaction in each of the following pairs would you expect to be faster?
(d) Thedisplacement byon bromomethane in benzene or in acetonitrile
Predict the product(s) for each elimination reaction below. In each case show the mechanism. What do the mechanisms have in common? Why?
a.
b.
c.
Compound X is optically inactive and has the formula. On treatment with strong base, X gives hydrocarbon Y,. Compound Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst and reacts with ozone to give two fragments. One fragment, Z, is an aldehyde with formula. The other fragment is glyoxal,. Write the reactions involved, and suggest structures for X, Y, and Z. What is the stereochemistry of X?
How might you prepare each of the following molecules using a nucleophilic substitution reaction at some step?
What do you think about this solution?
We value your feedback to improve our textbook solutions.