Phenylmagnesium bromide, generated by stirring 26.7g of bromobenzene and 3.9g of freshly cut magnesium in tetrahydrofuran, was added to a 12.0g ethyl benzoate solution in 30mL THF. After refluxing the reaction and subsequent workup, triphenylmethanol was produced. a. Determine the equivalents of each reagent compared to the primary reagent (ethyl benzoate.) b. Determine the percentage yield of the reaction if 19.0 g of the product were obtained.
Phenylmagnesium bromide, generated by stirring 26.7g of bromobenzene and 3.9g of freshly cut magnesium in tetrahydrofuran, was added to a 12.0g ethyl benzoate solution in 30mL THF. After refluxing the reaction and subsequent workup, triphenylmethanol was produced. a. Determine the equivalents of each reagent compared to the primary reagent (ethyl benzoate.) b. Determine the percentage yield of the reaction if 19.0 g of the product were obtained.
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:Phenylmagnesium bromide, generated by stirring 26.7g of bromobenzene and 3.9g of
freshly cut magnesium in tetrahydrofuran, was added to a 12.0g ethyl benzoate
solution in 30mL THF. After refluxing the reaction and subsequent workup,
triphenylmethanol was produced. a. Determine the equivalents of each reagent
compared to the primary reagent (ethyl benzoate.) b. Determine the percentage yield
of the reaction if 19.0 g of the product were obtained.
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