What is/are the principal product(s) formed when excess methylmagnesium iodide reacts with p-hydroxyacetophenone?

The end product will depend upon

a) the amount of the reagent taken

b) the final treatment of the reaction

If we have just taken methylmagnesium iodide and p-hydroxyacetophenone, then we will get methane and hydroxyl group substituted with MgI in place of hydrogen

Figure 1

However if we have taken excess of methylmagnesium iodide which is Grignard's reagent followed by hydrolysis we will get different product

Figure 2

personal, she chose to do it.

the correct answer is b. a strong acid completely dissociates to its ions when dissolved in water. completely dissociates to and ions. a is incorrect because does not fully ionize to and ions and some remain as the compound . c and d are incorrect because, and do not fall into the category of bronsted lowry acids. a bronsted lowry acid is a proton donor and since both molecules do not have a proton to donate they are not bronsted lowry acids. likewise,   if we use the lewis acid definition, they cannot be acids. a lewis acid is an electron pair acceptor. both and have a complete octet so can not accept any electrons which disqualifies them as acids.