1) Draw the mechanism for oxidation of any secondary alcohol with hypochlorous acid. This should be a step-wise curly arrow mechanism.

6. Complete the following reactions by providing the intermediate(s) and product(s). CH3OH, H

please answer parts b and c only

Draw the curved arrow mechanism for the acid-catalyzed hydration of  3,3-dimethyl-1-butene (using sulfuric acid).

Write the curved arrow mechanism for each of the following reactions.

Show a curved arrow mechanism for the following adol formation and dehydration.

Please don't provide hnad writtin solution...

a) Draw the structure of alkene and proposed reagent(s) used to prepare the product in Reaction A. Draw the reaction mechanism for first image  b) Predict the molecular structure of the major product(s) of Reaction B and C with second image   c) Rank the following compounds from the lowest to highest boiling point. Explain your answer briefly. A: 1-Butanoic acid;    B: 1- Butanol;     C: 1-Butane   d) Draw any three alcohol isomers with molecular formula of C4H10O.   e) Based on isomer structures you drawn in part (d), draw the final oxidation product(s) (by KMnO4/H+) of any two isomer, respectively.

B) 1. Provide TWO Grignard reactions, A and B, that can be used to make the provided target structure. Give the organic reactant and the Grignard reagent that would be used, you do not need to specify the aqueous acid workup step, but you must specify which of the C-C bonds is being made in the provided traget structure. Ignore stereochemistry in this question. To preview the image Click Here A) OH OH 2. Show how you would synthesize the target compound on the ri

Give correct detailed Solution with explanation needed of all ..don't give Handwritten answer..give correct solution