An allylic halide A with the chemical formula C5H9Cl undergoes an SN1 reaction with water to yield two isomer products B and C. Suggest structures for A, B, and C. Assign all peaks in the spectra for compounds B and C to the protons In your predicted structures.

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 the solution produced when 145 g of nacl is dissolved in sufficient water to prepare 2.75 l of solution?

1.17 mol hcl and 2.5 mol naoh react according to the equation hcl + naoh -> nacl + h2o . if the limiting reactant is hcl, determine the amount of excess reactant that remains. answer in units of mol.