CH,OH 'CI

Could you explain how to get answer

This is an example of a Base Catylized Nucleophilic Acyl Substitution. Specifically the mechanism is an example of base catylized alcoholysis analogous to what we have seen with carboxylic acid derivatives. Complete the curved-arrow mechanism for this reaction. NOTE: You can use H-A for acid and :B or -:A for base as needed. :0: Compound A :0: Compound B H H :0: : OMe :OME 1) K :0 H H :S: 2) : CI ما : OMe :S:

dont provide handwriting solution ..

3) Draw the complete curved arrow mechanism and the major product. Be sure to check for carbocation rearrangements. H-CI

Draw the curved arrow mechanism for the homolytic cleavage of the carbon-iodine bond in CH3l. H H

:&:&:&&&:&:&:&

Which of the following statement(s) is (are) FALSE?a. In the hydroxylation of alkenes, reaction of alkenes with hot, basic permanganate solution results to syn addition product.b. In the hydroxylation of alkenes, reaction of alkenes with cold, basic permanganate solution results to anti addition product.c. In the hydroxylation of alkenes, reaction of alkenes with hot, basic permanganate solution results to anti addition product.d. Both B& C only.e. All of the above.

Give detailed Solution with explanation needed..give correct answer please...please draw all bonds and chiral center

Please don't provide handwritten solution .....