Free radical Brormination is a slower reaction than chlorination but it is a synthetic route often used to make alky bromides. Alkyl fluorides are not made byFree Radical Halongenation. Explain why free radical Fluorinationis not a viable route of synthesis for thesecompounds(show your workto support your claim all math calculationsof the reaction enthalpy). (5pts).

Determine the wavelength of the light absorbed when an electron in a hydrogen atom makes a transition from an orbital in the n=3 level to an orbital in the n=7 level.

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.

How would the number of moles (n) of o2 change if the atmospheric pressure doubled but all other variables stayed the same