Starting materials used; - 1mL sebacoyl chloride - 50 mL hexane - 2.5 mL 1,6-diaminohexane -...
Starting materials used;
- 1mL sebacoyl chloride
- 50 mL hexane
- 2.5 mL 1,6-diaminohexane
- 25 mL 3% sodium hydroxide
Final products;
- 0.94 g adipic acid
- 1,6-hexamethylenediamine
Calculate the theoretical yield adipic acid if the actual yield is 0.94g?
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Starting materials used;
- 1mL sebacoyl chloride
- 50 mL hexane
- 2.5 mL 1,6-diaminohexane
-...
* Densities of the two reactants are: Sebacoyl chloride 1.121 g/mL and, 1,6-diaminohexane 0.83 g/mL yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3...
* Densities of the two reactants are: Sebacoyl chloride 1.121
g/mL and, 1,6-diaminohexane 0.83 g/mL
yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3 mL 1,6- diaminohexane and end up with 3.30g of my product nylon 6,10 what is my percent yield?
yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3 mL 1,6- diaminohexane and end up with 3.30g of...
10 mL of 0.59M 1,6-diaminohexane and 10 mL of 0.29M Sebacoyl chloride are used to make nylon 6.10. The final product weight was 1.36g. Calculate the percent yield? Use the MW of one repeating monomer...
10 mL of 0.59M 1,6-diaminohexane and 10 mL of 0.29M Sebacoyl chloride are used to make nylon 6.10. The final product weight was 1.36g. Calculate the percent yield? Use the MW of one repeating monomer for the weight of the product? Please show all work.
How to calculate theoretical yield & actual yield for this problem. A student used 3 mL...
How to calculate theoretical yield & actual yield for this
problem.
A student used 3 mL propanal and an equimolar amount of acetophenone as starting materials for the aldol condensation experiment. Sodium hydroxide was used for the base and ethanol was used for the solvent. After refluxing and purification, He/She obtained 3.9 g of the product.
Starting Materials: 0.25 4-Aminobenzoic Acid mL; _moles Ethyl Alcohol 2.5 mL; moles BA 0.3 Conc. H2SO4...
Starting Materials: 0.25 4-Aminobenzoic Acid mL; _moles Ethyl Alcohol 2.5 mL; moles BA 0.3 Conc. H2SO4 mL; moles Product: 0.08 g of product Formula Weight: g/mole; Isolated Yield: -8; Yield Appearance:
Calculate the theoretical yield and percent yield for experiments 7, 8, and 9. For experiment 9,...
Calculate the theoretical yield and percent yield for
experiments 7, 8, and 9. For experiment 9, determine the
theoretical yield based on starting with 0.50g of 3-nitrobenzoic
acid. Show work
Acid I (experiment 7): Weight of methyl 3-nitrobenzoate = 1.9
g
Acid II (experiment 8): Weight of 3-nitrobenzoic acid = 1.75
g
Acid III (experiment 9): Weight of 3-nitrobenzamide = 0.30 g
Experiment 7:
-2.5 mL concentrated H2SO4
-1.75 mL concentrated HNO3 (16M)
-2.1 mL concentrated Methyl Benzoate
Experiment 8:...
Suppose 1.00 g of NaOH is used to prepare 250 mL of an NaOH solution. Compare...
Suppose 1.00 g of NaOH is used to prepare 250 mL of an NaOH solution. Compare the expected molarity of this solution to the actual average molarity you measured in the standardization. What do you notice? Do you think the results would have been more accurate if a different type of acid or base were used in the standardization? Why, or why not? There are many different primary standards that could be used in a standardization titration. What are the...
Calculate the theoretical yield for Orange II (mw= 422g/mol; experimental weight of orange II azo-dye=0.4g). EXPERIMENTAL...
Calculate the theoretical yield for Orange II (mw= 422g/mol;
experimental weight of orange II azo-dye=0.4g).
EXPERIMENTAL Calculate the theoretical yield before the lab. Caution: Orange II dyes clothing and other organic materials a permanent unique orange. As a measure of your technique, points may be subtracted for orange hands, etc. 1 DIAZOTIZATION OF SULFANILIC ACID Dissolve 0.4 g of anhydrous sodium carbonate in 7.5 mL of H.O. Use a 25 mL Erlenmever flask. 2. Add 0.45 g of sulfanilic acid...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the experimental section above) H2SO4 + Na2Cr207 2H20- H2O, A Molecular Weight Theoretical yield amount moles on (if applicable) Equivalents 2. Look up the melting point for p-nitrobenzoic acid and record the reference. 3. What color change is expected to be observed in the reaction? Explain why. CHROMIC ACID OXIDATION Experimental Procedure: Part I: Synthesis of p-nitrobenzoic Acid 1. Under the hood, add 0.400 g...
what is the theoretical yield for this experiment? ORGANIC POLYMERS: THE SYNTHESIS OF NYLON Nylon's outstanding...
what is the theoretical yield for this experiment?
ORGANIC POLYMERS: THE SYNTHESIS OF NYLON Nylon's outstanding characteristic in the textile industry is its versatility. It can be made strong enough to stand up under the punishment tire cords must endure, fine enough for sheer, high fashion hosiery, and light enough for parachute cloth and backpacker's tents. Nylon is used both alone and in blends with other fibers, where its chief contributions are strength and abrasion resistance. Nylon washes easily, dries...
in FRIEDEL-CRAFTS ACYLATION AND COLUMN CHROMATOGRAPHY lab (2 pts) Amount of acetyl chloride used ____4______(drops) (each...
in FRIEDEL-CRAFTS ACYLATION AND COLUMN CHROMATOGRAPHY lab
(2 pts) Amount of acetyl chloride used ____4______(drops) (each
drop is 0.01 mL) _____2______(equivalents) Based on the amount of
ferrocene you began the Friedel-Crafts reaction with, determine the
percent yield of acetylferrocene, diacetylferrocene, and the
percent recovery of unreacted ferrocene (show work)
react by 0.100 g of ferrocene at beginning
got 0 g of ferrocene, 0.012g of diacetylferrocene , 0.017g of
acetylferrocene
REACTION PROCEDURE: To a 5 mL conical vial, add a spin...
* Densities of the two reactants are: Sebacoyl chloride 1.121
g/mL and, 1,6-diaminohexane 0.83 g/mL
yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3 mL 1,6- diaminohexane and end up with 3.30g of my product nylon 6,10 what is my percent yield?
yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3 mL 1,6- diaminohexane and end up with 3.30g of...
How to calculate theoretical yield & actual yield for this
problem.
A student used 3 mL propanal and an equimolar amount of acetophenone as starting materials for the aldol condensation experiment. Sodium hydroxide was used for the base and ethanol was used for the solvent. After refluxing and purification, He/She obtained 3.9 g of the product.
Starting Materials: 0.25 4-Aminobenzoic Acid mL; _moles Ethyl Alcohol 2.5 mL; moles BA 0.3 Conc. H2SO4 mL; moles Product: 0.08 g of product Formula Weight: g/mole; Isolated Yield: -8; Yield Appearance:
Calculate the theoretical yield and percent yield for
experiments 7, 8, and 9. For experiment 9, determine the
theoretical yield based on starting with 0.50g of 3-nitrobenzoic
acid. Show work
Acid I (experiment 7): Weight of methyl 3-nitrobenzoate = 1.9
g
Acid II (experiment 8): Weight of 3-nitrobenzoic acid = 1.75
g
Acid III (experiment 9): Weight of 3-nitrobenzamide = 0.30 g
Experiment 7:
-2.5 mL concentrated H2SO4
-1.75 mL concentrated HNO3 (16M)
-2.1 mL concentrated Methyl Benzoate
Experiment 8:...
Calculate the theoretical yield for Orange II (mw= 422g/mol;
experimental weight of orange II azo-dye=0.4g).
EXPERIMENTAL Calculate the theoretical yield before the lab. Caution: Orange II dyes clothing and other organic materials a permanent unique orange. As a measure of your technique, points may be subtracted for orange hands, etc. 1 DIAZOTIZATION OF SULFANILIC ACID Dissolve 0.4 g of anhydrous sodium carbonate in 7.5 mL of H.O. Use a 25 mL Erlenmever flask. 2. Add 0.45 g of sulfanilic acid...
CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the experimental section above) H2SO4 + Na2Cr207 2H20- H2O, A Molecular Weight Theoretical yield amount moles on (if applicable) Equivalents 2. Look up the melting point for p-nitrobenzoic acid and record the reference. 3. What color change is expected to be observed in the reaction? Explain why. CHROMIC ACID OXIDATION Experimental Procedure: Part I: Synthesis of p-nitrobenzoic Acid 1. Under the hood, add 0.400 g...
what is the theoretical yield for this experiment?
ORGANIC POLYMERS: THE SYNTHESIS OF NYLON Nylon's outstanding characteristic in the textile industry is its versatility. It can be made strong enough to stand up under the punishment tire cords must endure, fine enough for sheer, high fashion hosiery, and light enough for parachute cloth and backpacker's tents. Nylon is used both alone and in blends with other fibers, where its chief contributions are strength and abrasion resistance. Nylon washes easily, dries...
in FRIEDEL-CRAFTS ACYLATION AND COLUMN CHROMATOGRAPHY lab
(2 pts) Amount of acetyl chloride used ____4______(drops) (each
drop is 0.01 mL) _____2______(equivalents) Based on the amount of
ferrocene you began the Friedel-Crafts reaction with, determine the
percent yield of acetylferrocene, diacetylferrocene, and the
percent recovery of unreacted ferrocene (show work)
react by 0.100 g of ferrocene at beginning
got 0 g of ferrocene, 0.012g of diacetylferrocene , 0.017g of
acetylferrocene
REACTION PROCEDURE: To a 5 mL conical vial, add a spin...
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