When 2-methyl-1-butene is treated with in dichloromethane, the major product is 1-bromo-2-methyl-2-butene . Account for the formation of this product by drawing the structure of the most stable radical intermediate. Include all valence lone pairs in your answer. Include all valence radical electrons in your answer.
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Match the name of the following compound: mgso4 · h2omagnesium sulfate monohydratemagnesium (ii) sulfate monohydratemagnesium (ii) sulfate hydratemagnesium sulfate hydrate
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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.
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Chemistry, 22.06.2019 08:30
In the millikan oil drop experiment they determined that every drop had a charge which was a while number multiple of -1.60x10^-19. if a drop has a total charge of -9.60x10^-19 then how many excess electrons are contained within the drop?
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When 2-methyl-1-butene is treated with in dichloromethane, the major product is 1-bromo-2-methyl-2-b...
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