Synthesis of ethy trans-cinnamate via claisen condensation reaction: In the claisen condensation reaction, reacting ethyl acetate,...
Synthesis of ethy trans-cinnamate via claisen condensation reaction: In the claisen condensation reaction, reacting ethyl acetate, sodium ethoxide and benzaldehyde often produces a yellow solid. What could the solid be and why does it disappear during the workup stage?
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Synthesis of ethy trans-cinnamate via claisen condensation
reaction: In the claisen condensation reaction, reacting ethyl
acetate,...
When ethyl acetate is treated with sodium ethoxide followed by mild aqueous acid a Claisen condensation...
When ethyl acetate is treated with sodium ethoxide followed by mild aqueous acid a Claisen condensation product results. Write a mechanism using the usual conventions and provide an unambiguous structural formula for the final product.
This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt Condensation The Chalcone starting materials are: p-bromoscetophenone (solid)...
This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt
Condensation
The Chalcone starting materials are:
p-bromoscetophenone (solid)
p-chlorobenzaldehyde (solid)
11. [3 points) Draw the curved-arrow mechanism for your chalcone from the starting materials that you used. Explain why this reaction produces only one chalcone and not a mixture.
This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt Condensation The Chalcone starting materials are: p-bromoscetophenone (solid)...
This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt
Condensation
The Chalcone starting materials are:
p-bromoscetophenone (solid)
p-chlorobenzaldehyde (solid)
6. [1pt] When you treated the reaction TLC with 2,4-dinitrophenylhydrazine solution, you must have observed that the starting materials show up as bright orange spots instantaneously, whereas the product either shows no change or appears as a faint spot. Explain this observation. 8. [1 pt] 4-chlorobenzaldehyde and 4-bromoacetophenone are both solid starting materials for the synthesis of substituted chalcone. When both of...
Choose the correct answer and explain why you choose that answer. -Page 2 4. The Claisen...
Choose the correct answer and explain why you choose that
answer.
-Page 2 4. The Claisen condensation produces which of these? a- An α-keto ester b.AB-keto ester C, A β-hydroxy ester d. A B-hydroxyaldehyde e. A B-di ketone 5. Which compound could be prepared using a Michael reaction? 0 0 o 1 CCH3 СОС2HS a. I d. IV e. v Part 2 t. The product (s) of the reaction of 2 mol of ethyl butanoate sodium ethoxide is(are) : b....
SYNTHESIS OF trans-p-ANISALACETOPHENONE Prepare a table of all chemicals used in the procedure with their purpose...
SYNTHESIS OF trans-p-ANISALACETOPHENONE
Prepare a table of all chemicals used in the procedure with
their purpose
Melting point of trans-p-anisalacetophenone (with source) and
Molar mass of trans-p-anisalacetophenone (with source) (i cant find
these two things anywhere)
Procedure: 1. Carefully measure 1.0 mL each of p-anisaldehyde and acetophenone and place them in a screw-cap testtube. 2. To this add 3.0 mL of 95% ethanol. Shake the test tube gently to achieve a homogenous mixture. 3. Add 6-7 drops of 40% sodium...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...
Give a detailed mechanism for this reaction and give a separation scheme NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis...
Give a detailed mechanism for this reaction and give a separation
scheme
NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis of an Ester Isoamyl acetate (Banana Oil) Purpose This experiment demonstrat and alcohol. The technique of refluxing the reaction mixture is introduced. es the procedure for the synthesis of an ester from a carboxylic acid Esters are an important functional group in organic chemistry, and esters are found widely distributed in nature. Many lower molecular weight esters are associated with natural fuit flavors and...
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepa...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
QUESTIONS TO ANSWER: Prepare a table of all chemicals used with the structure and purpose of...
QUESTIONS TO ANSWER:
Prepare a table of all chemicals used with the structure and
purpose of each.
Calculate the theoretical yield by finding limiting reactant of
the experiment by converting reactants to product (remember to show
all calculations used)
Calculate the percent yield using the limiting reactant
Calculate the Rf for triphenylmethanol. If there are two dots,
determine which one is triphenylmethanol.. ( I did not provide
data. Please let me know how I Would do this if I did)...
What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this...
What is the theoretical yield (in grams) and percent yield of your
triphenylmethanol product in this experiment? (Weight of
triphenylmethanol: 0.060g)
BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...
This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt
Condensation
The Chalcone starting materials are:
p-bromoscetophenone (solid)
p-chlorobenzaldehyde (solid)
11. [3 points) Draw the curved-arrow mechanism for your chalcone from the starting materials that you used. Explain why this reaction produces only one chalcone and not a mixture.
This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt
Condensation
The Chalcone starting materials are:
p-bromoscetophenone (solid)
p-chlorobenzaldehyde (solid)
6. [1pt] When you treated the reaction TLC with 2,4-dinitrophenylhydrazine solution, you must have observed that the starting materials show up as bright orange spots instantaneously, whereas the product either shows no change or appears as a faint spot. Explain this observation. 8. [1 pt] 4-chlorobenzaldehyde and 4-bromoacetophenone are both solid starting materials for the synthesis of substituted chalcone. When both of...
Choose the correct answer and explain why you choose that
answer.
-Page 2 4. The Claisen condensation produces which of these? a- An α-keto ester b.AB-keto ester C, A β-hydroxy ester d. A B-hydroxyaldehyde e. A B-di ketone 5. Which compound could be prepared using a Michael reaction? 0 0 o 1 CCH3 СОС2HS a. I d. IV e. v Part 2 t. The product (s) of the reaction of 2 mol of ethyl butanoate sodium ethoxide is(are) : b....
SYNTHESIS OF trans-p-ANISALACETOPHENONE
Prepare a table of all chemicals used in the procedure with
their purpose
Melting point of trans-p-anisalacetophenone (with source) and
Molar mass of trans-p-anisalacetophenone (with source) (i cant find
these two things anywhere)
Procedure: 1. Carefully measure 1.0 mL each of p-anisaldehyde and acetophenone and place them in a screw-cap testtube. 2. To this add 3.0 mL of 95% ethanol. Shake the test tube gently to achieve a homogenous mixture. 3. Add 6-7 drops of 40% sodium...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...
Give a detailed mechanism for this reaction and give a separation
scheme
NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis of an Ester Isoamyl acetate (Banana Oil) Purpose This experiment demonstrat and alcohol. The technique of refluxing the reaction mixture is introduced. es the procedure for the synthesis of an ester from a carboxylic acid Esters are an important functional group in organic chemistry, and esters are found widely distributed in nature. Many lower molecular weight esters are associated with natural fuit flavors and...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
QUESTIONS TO ANSWER:
Prepare a table of all chemicals used with the structure and
purpose of each.
Calculate the theoretical yield by finding limiting reactant of
the experiment by converting reactants to product (remember to show
all calculations used)
Calculate the percent yield using the limiting reactant
Calculate the Rf for triphenylmethanol. If there are two dots,
determine which one is triphenylmethanol.. ( I did not provide
data. Please let me know how I Would do this if I did)...
What is the theoretical yield (in grams) and percent yield of your
triphenylmethanol product in this experiment? (Weight of
triphenylmethanol: 0.060g)
BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...
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