Calculate the mass of 10.0 mmol of trans-cinnamic acid and the theoretical yield of 2,3-dibromopropanoic acid.
Calculate the mass of 10.0 mmol of trans-cinnamic acid and the theoretical yield of 2,3-dibromopropanoic acid.
Calculate the theoretical yield of 2,3-dibromo-3-phenylpropanoic acid in 0.7 mmol of trans-cinnamic acid in both mg and mmol.
Bromunation of trans-Cinnamic Acid Show the calculations for the theoretical yield (in grams) of the diromide product). There are 0.017 mol of Cinnamic Acid and 0.020 mol of Pyridinium Tribromide.
What is the theoretical yield of 1mmol of trans cinnamic acid+1.2 mmols of pyridinium tribromide and what product is made? please note in this reaction acetic acid is added making me believe it is a catalyst.
what is 0.7 mmol of trans-cinnamic acid converted into mg?
What is the stereochemical outcome of reacting trans-cinnamic acid with bromine to form 2,3-dibromopropanoic acid? Please post answer asap thank you! B2 OH Stereochemistry of both bonded bromines?
[1]. (a) Calculate the theoretical yield of 1-bromobutane in volume and mass when 72.0 mmol of 1-butanol react. (b) Calculate the theoretical yield of 2-bromobutane in volume and mass when 72.0 mmol of 2-butanol react. CH3 (CH2 3OH HBr H2O C4H9Br
Draw the mechanism of the bromination reaction between trans cinnamic acid and bromine. Be sure to include stereochemistry( wedge and dashed structures). The product obtained was the racemic mixture of (2R,3S) and (2S,3R) of 2,3-dibromo-3-phenylpropanoic acid.
Suppose a student started with 133.0 mg of trans-cinnamic acid, 443 mg of pyridinium tribromide, and 2.60 mL of glacial acetic acid. After the reaction and workup, the student ended up with 0.1683 g of brominated product. Calculate the student\'s theoretical and percent yields.
Calculate the theoretical yield of 2,3-epoxynorbornane based on using 100. mg of norbornene. 2. Calculate the theoretical yield of 2,3-epoxynorbornane based on using 100. mg of of norbornene.
An Alkene addition is being performed. The reactants are .1504 g of trans-cinnamic acid and .3843 g of pyridinium tribromide, these components heated and are reacted within 2 mL of glacial acetic acid to produce 2,3-dibromo-3-phenylpropanoic acid. How much of this final product would theoretically be produced? Would the product be majority threo or erythro?