Please calculate theoretical grams of if 1.10 grams where collected in part 1 and 1.08 grams where collected part 2. Also calculate percent yeild. Reaction Conditions 1 1) In a 50-mL round-bottomed flask, with a spin bar, add 10mL of H2O solution which contains 1.0 mmol of 2-acetylpyridine. Stir the mixture vigorously. 2) Place 1.0 mmol of 4-nitrobenzaldehyde in a separate vial and dissolve using a minimum amount of warm MeOH. While still warm, add the solution of 4-nitrobenzaldehyde to the stirring mixture in the round-bottomed flask from step 1. 3) To this mixture add 0.25 mmol of Na2CO3 dissolved in 5 mL of H₂O. 4) After 1 hr of vigorous stirring, collect the solid product using vacuum filtration and wash with H2O (3 x 10mL) and a minimal amount of cold MeOH. 5) Allow the product to dry on the vacuum, determine the yield, melting point. Reaction Conditions 2 1) In a 50-mL round-bottomed flask, with a spin bar, add 10mL of H2O solution which contains 1.0 mmol of 2-acetylpyridine. Stir the mixture vigorously. 2) Place 1.0 mmol of 4-nitrobenzaldehyde in a separate vial and dissolve using a minimum amount of warm MeOH. While still warm, add the solution of 4-nitrobenzaldehyde to the stirring mixture in the round-bottomed flask. 3) To this mixture add 0.25 mmol of Na2CO3 dissolved in 5 mL of H₂O. 4) Attach a water-cooled reflux condenser and heat the reaction to reflux using an oil bath or a heating mantle. 5) After 1 hr of vigorous stirring at reflux, cool the reaction using an ice-water bath, collect the solid product using vacuum filtration. Wash the solid with H₂O (3 x 10mL) and a minimal amount of cold MeOH. 6) Allow the product to dry on the vacuum, determine the yield, melting point.
Please calculate theoretical grams of if 1.10 grams where collected in part 1 and 1.08 grams where collected part 2. Also calculate percent yeild. Reaction Conditions 1 1) In a 50-mL round-bottomed flask, with a spin bar, add 10mL of H2O solution which contains 1.0 mmol of 2-acetylpyridine. Stir the mixture vigorously. 2) Place 1.0 mmol of 4-nitrobenzaldehyde in a separate vial and dissolve using a minimum amount of warm MeOH. While still warm, add the solution of 4-nitrobenzaldehyde to the stirring mixture in the round-bottomed flask from step 1. 3) To this mixture add 0.25 mmol of Na2CO3 dissolved in 5 mL of H₂O. 4) After 1 hr of vigorous stirring, collect the solid product using vacuum filtration and wash with H2O (3 x 10mL) and a minimal amount of cold MeOH. 5) Allow the product to dry on the vacuum, determine the yield, melting point. Reaction Conditions 2 1) In a 50-mL round-bottomed flask, with a spin bar, add 10mL of H2O solution which contains 1.0 mmol of 2-acetylpyridine. Stir the mixture vigorously. 2) Place 1.0 mmol of 4-nitrobenzaldehyde in a separate vial and dissolve using a minimum amount of warm MeOH. While still warm, add the solution of 4-nitrobenzaldehyde to the stirring mixture in the round-bottomed flask. 3) To this mixture add 0.25 mmol of Na2CO3 dissolved in 5 mL of H₂O. 4) Attach a water-cooled reflux condenser and heat the reaction to reflux using an oil bath or a heating mantle. 5) After 1 hr of vigorous stirring at reflux, cool the reaction using an ice-water bath, collect the solid product using vacuum filtration. Wash the solid with H₂O (3 x 10mL) and a minimal amount of cold MeOH. 6) Allow the product to dry on the vacuum, determine the yield, melting point.
Chemistry
10th Edition
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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![Please calculate theoretical grams of if 1.10 grams
where collected in part 1 and 1.08 grams where
collected part 2. Also calculate percent yeild.
Reaction Conditions 1
1) In a 50-mL round-bottomed flask, with a spin bar, add 10mL of H2O solution which contains 1.0
mmol of 2-acetylpyridine. Stir the mixture vigorously.
2) Place 1.0 mmol of 4-nitrobenzaldehyde in a separate vial and dissolve using a minimum
amount of warm MeOH. While still warm, add the solution of 4-nitrobenzaldehyde to the
stirring mixture in the round-bottomed flask from step 1.
3) To this mixture add 0.25 mmol of Na2CO3 dissolved in 5 mL of H₂O.
4) After 1 hr of vigorous stirring, collect the solid product using vacuum filtration and wash with
H2O (3 x 10mL) and a minimal amount of cold MeOH.
5) Allow the product to dry on the vacuum, determine the yield, melting point.
Reaction Conditions 2
1) In a 50-mL round-bottomed flask, with a spin bar, add 10mL of H2O solution which contains 1.0
mmol of 2-acetylpyridine. Stir the mixture vigorously.
2) Place 1.0 mmol of 4-nitrobenzaldehyde in a separate vial and dissolve using a minimum
amount of warm MeOH. While still warm, add the solution of 4-nitrobenzaldehyde to the
stirring mixture in the round-bottomed flask.
3) To this mixture add 0.25 mmol of Na2CO3 dissolved in 5 mL of H₂O.
4) Attach a water-cooled reflux condenser and heat the reaction to reflux using an oil bath or a
heating mantle.
5) After 1 hr of vigorous stirring at reflux, cool the reaction using an ice-water bath, collect the
solid product using vacuum filtration. Wash the solid with H₂O (3 x 10mL) and a minimal
amount of cold MeOH.
6) Allow the product to dry on the vacuum, determine the yield, melting point.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F6d6d9f59-10ca-4029-9edc-157229a6e76d%2Fb55d0134-8f31-477b-997d-eb07b41fb557%2Flj986qo_processed.png&w=3840&q=75)
Transcribed Image Text:Please calculate theoretical grams of if 1.10 grams
where collected in part 1 and 1.08 grams where
collected part 2. Also calculate percent yeild.
Reaction Conditions 1
1) In a 50-mL round-bottomed flask, with a spin bar, add 10mL of H2O solution which contains 1.0
mmol of 2-acetylpyridine. Stir the mixture vigorously.
2) Place 1.0 mmol of 4-nitrobenzaldehyde in a separate vial and dissolve using a minimum
amount of warm MeOH. While still warm, add the solution of 4-nitrobenzaldehyde to the
stirring mixture in the round-bottomed flask from step 1.
3) To this mixture add 0.25 mmol of Na2CO3 dissolved in 5 mL of H₂O.
4) After 1 hr of vigorous stirring, collect the solid product using vacuum filtration and wash with
H2O (3 x 10mL) and a minimal amount of cold MeOH.
5) Allow the product to dry on the vacuum, determine the yield, melting point.
Reaction Conditions 2
1) In a 50-mL round-bottomed flask, with a spin bar, add 10mL of H2O solution which contains 1.0
mmol of 2-acetylpyridine. Stir the mixture vigorously.
2) Place 1.0 mmol of 4-nitrobenzaldehyde in a separate vial and dissolve using a minimum
amount of warm MeOH. While still warm, add the solution of 4-nitrobenzaldehyde to the
stirring mixture in the round-bottomed flask.
3) To this mixture add 0.25 mmol of Na2CO3 dissolved in 5 mL of H₂O.
4) Attach a water-cooled reflux condenser and heat the reaction to reflux using an oil bath or a
heating mantle.
5) After 1 hr of vigorous stirring at reflux, cool the reaction using an ice-water bath, collect the
solid product using vacuum filtration. Wash the solid with H₂O (3 x 10mL) and a minimal
amount of cold MeOH.
6) Allow the product to dry on the vacuum, determine the yield, melting point.
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