A. If the benzophenone used to prepare triphenylmethanol was wet, what organic by-product would form?

Question

A. If the benzophenone used to prepare triphenylmethanol was wet, what organic by-product would form?
B. How do you write a stepwise mechanism for triphenylmethanol (diethylcarbonate w/ phenylmagnesium bromide)?

Answer 1

A) Benzene (PhMgBr + H2O -> C6H6 + Mg(OH)Br)

B) The carbonyl carbon is attacked.

Answer 2

not all "typical manufacturers" are non-organic and organic. Non-organic and organic products artwork for some those with particular skin circumstances, however the climate may be too lively, and consequence in a wreck out in delicate skin as a results of inflammation. i discover organic and organic products "greater secure" to apply, quite in skins that are greater carriers to sensitivity. in spite of the incontrovertible fact that, you may desire to be allergic to between the plant extracts after all. There are professional's and con's to employing the two organic and organic, and non-organic and organic.