Write two different resonance forms for triphenylmethyl cation. Write the structure showing the positive charge at an ortho position.

The scheme below is from a series of reactions that are part of a synthesis of vitamin a. answer the following questions with reference to this scheme. (i) what is "reagent a"? (ii) draw a step-by-step mechanism which explains the formation of compound c from compound b (iii) which reagents would you use to form compound e from compounds c and d (reagents b and c)? for each reagent suggested above in (ii) explain the role of the reagent in the reaction to (iv) form compound e. you may wish to do this by drawing a mechanism. 1. addition of reagent a но reagent a 2. н,о" thо oh нон-с compound a. compound b. compound c .ch-оh 1. reagent b "сно 2. reagent c сh oh compound e. compound d.

What is the molarity of 60.0 grams of naoh dissolved in 750 milliliters of water? a) 1.1 m b) 2.0 m c) 12 m d) 75 m

What is the empirical formula of c6h18o3? ch3o c2h5o c2h6o c2h5o5