3- During the Aldol condensation experiment you add 1.7 mL of benzaldehyde (MW - 106.12 g/mol, density - 1.044 g/mL) to 1.3 mL of acetophenone (MW - 120.4 g/ mol, density - 1.03 g/mL) and 0.31 g of NaOH (MW - 40.0 g/mol, dens - 2.13 g/mL) You run the reaction as outlined in the lab manual.What is the theoretical yield in grams of the product (E)-chalcone (MW - 208.26 g/mol) ? 6- During the Wittig reaction, you perform the reaction as follows:4-chlorobenzaldehyde (136 mg) and (carbethoxymethylene)triphenylphosphorane(323 mg) were placed in a 25 mL Erlenmeyer flask. The two solids were mixed vigorously for 15 min. The reaction mixture was diluted with hexanes (2.9 mL - density 0.661 g/mL) The by-product, triphenylphosphine oxide, was filtered off.0.085 g total of triphenyl phosphine was isolated. The filtrate was then evaporated to dryness to obtain 0.151 g of the desired product, pure ethyl-4-chlorocinnamate, as a colorless oil.What is the % effective mass yield of the reaction? (Your result should be reported as a % value and rounded to the nearest integer.

Introduction to General, Organic and Biochemistry
11th Edition
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Chapter14: Alcohols, Ethers, And Thiols
Section: Chapter Questions
Problem 14.26P
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3- During the Aldol condensation experiment you add 1.7 mL of benzaldehyde (MW - 106.12 g/mol, density - 1.044 g/mL) to 1.3 mL of acetophenone (MW - 120.4 g/ mol, density - 1.03 g/mL) and 0.31 g of NaOH (MW - 40.0 g/mol, dens - 2.13 g/mL) You run the reaction as outlined in the lab manual.
What is the theoretical yield in grams of the product (E)-chalcone (MW - 208.26 g/mol) ?

6- During the Wittig reaction, you perform the reaction as follows:
4-chlorobenzaldehyde (136 mg) and (carbethoxymethylene)triphenylphosphorane
(323 mg) were placed in a 25 mL Erlenmeyer flask. The two solids were mixed vigorously for 15 min. The reaction mixture was diluted with hexanes (2.9 mL - density 0.661 g/mL) The by-product, triphenylphosphine oxide, was filtered off.
0.085 g total of triphenyl phosphine was isolated. The filtrate was then evaporated to dryness to obtain 0.151 g of the desired product, pure ethyl-4-chlorocinnamate, as a colorless oil.
What is the % effective mass yield of the reaction? (Your result should be reported as a % value and rounded to the nearest integer.

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