Epoxide Ring-Opening Post Lab Question: There was a marked difference in the final product distribution from...
Epoxide Ring-Opening Post Lab Question:
There was a marked difference in the final product distribution from this weeks acid-catalyzed reaction versus the base-catalyzed reaction. Was one set of reaction conditions more regiospecific than the other? If so, why do you think that this was the case? Explain your reasoning in detail.
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Epoxide Ring-Opening Post Lab Question:
There was a marked difference in the final product distribution
from...
Epoxide Ring Opening Post Lab Questions: 1 Reflux conditions are problematic when performing acid catalyzed epoxide...
Epoxide Ring Opening Post Lab Questions: 1 Reflux conditions are problematic when performing acid catalyzed epoxide ring opening reactions. Provide the potential side product(s) that would result from carrying out the following reaction under reflux conditions. You must be sure to show the side products of both the major and minors products of the reaction below: . 3PO4 Methanol Reflux
Why would it be problematic to perform an acid catalyzed epoxide ring opening reaction under reflux...
Why would it be problematic to perform an acid catalyzed epoxide ring opening reaction under reflux conditions? Be specific. Provide the potential side product(s) that would result from carrying out the following reactions under reflux conditions. Hint
Please help with the question that I have circled in red. This is from a lab...
Please help with the question that I have circled in red. This
is from a lab I did and I have included the entire handout in case
it helps you to answer the question.
2015 Chem 263 2-Credit Org Lab 6T: Dehydration of Cyclohexanol to Cyclohexene Lab 6T w lecture you recently learned that alkenes undergo acid-catalyzed addition of H20 (hydration of the alkene) to yield alcohols. This lab with illustrate the same chemistry in reverse; the microscopic reverse of...
Saponification Reaction (HINT: See your post-lab question from last week) moles 1 equivalents! Mw...
Saponification Reaction (HINT: See your post-lab question from last week) moles 1 equivalents! Mw (g/mol)-Density (g/mL) Amount Compound Methyl cinnamate KOH MeOH Cinnamic acid product 162.19 56.11 32.04 1.09 2.12 0.79 N/A produet mL NA Experimental: 1. Set up a water bath and maintain at a temperature of roughly 35°C. 2. Combine the cinnamate, KOH, and methanol into the 25 ml round bottom flask. 3. Position the flask into the water bath so that the water of the bath rests...
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...
Organic chemistry post-lab question: "Why is important to add the alkyl halide dropwise in your reaction?...
Organic chemistry post-lab question: "Why is important
to add the alkyl halide dropwise in your reaction? (Hint: your
reaction is not heated, but you still need a water-cooled
condenser!)" Please answer in detail!
Here is a copy of the experiment, thank you!
The Grignard reaction is an important synthetic process by which a carbon-carbon bond is formed. Magnesium metal is first reacted with an organic halide. The resultant organo-magnesium halide (Grignard reagent) is then combined with a carbonyl compound, ultimately...
Synthesis of dimedone This lab exercise will give you practical experience with the generation of...
Synthesis of dimedone This lab exercise will give you practical experience with the generation of a malonic ester enolate and subsequent reaction with an a,p-unsaturated carbonyl compound. This sequence is known as the Michael reaction. In the presence of sodium methoxide, dimethyl propanedioate (malonic ester/dimethyl malonate) is converted to the corresponding enolate anion and reaction with 4-methylpent-3-en-2-one (mesityl oxide) affords the Michael adduct 1, as shown in the reaction sequence below. Under the basic reaction conditions, the Michael adduct 1...
Synthesis of dimedone This lab exercise will give you practical experience with the generation of...
Synthesis of dimedone This lab exercise will give you practical experience with the generation of a malonic ester enolate and subsequent reaction with an a,p-unsaturated carbonyl compound. This sequence is known as the Michael reaction. In the presence of sodium methoxide, dimethyl propanedioate (malonic ester/dimethyl malonate) is converted to the corresponding enolate anion and reaction with 4-methylpent-3-en-2-one (mesityl oxide) affords the Michael adduct 1, as shown in the reaction sequence below. Under the basic reaction conditions, the Michael adduct 1...
Working on the questions at the end of this lab report (see above). I need help answering questio...
Working on the questions at the end of this lab report
(see above). I need help answering questions 2, 3, and 4 completely
and thoroughly. Thank you!
s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...
It's a weak acid strong base titration Experiment 4: Identification of an unknown acid by titration...
It's a weak acid strong base titration
Experiment 4: Identification of an unknown acid by titration Page 2 of 15 Background In this experiment, you will use both qualitative and quantitative properties to determine an unknown acid's identity and concentration. To do this analysis, you will perform a titration of your unknown acid sample-specifically a potentiometric titration where you use a pH meter and record pH values during the titration, combined with a visual titration using a color indi- cator...
Epoxide Ring Opening Post Lab Questions: 1 Reflux conditions are problematic when performing acid catalyzed epoxide ring opening reactions. Provide the potential side product(s) that would result from carrying out the following reaction under reflux conditions. You must be sure to show the side products of both the major and minors products of the reaction below: . 3PO4 Methanol Reflux
Please help with the question that I have circled in red. This
is from a lab I did and I have included the entire handout in case
it helps you to answer the question.
2015 Chem 263 2-Credit Org Lab 6T: Dehydration of Cyclohexanol to Cyclohexene Lab 6T w lecture you recently learned that alkenes undergo acid-catalyzed addition of H20 (hydration of the alkene) to yield alcohols. This lab with illustrate the same chemistry in reverse; the microscopic reverse of...
Saponification Reaction (HINT: See your post-lab question from last week) moles 1 equivalents! Mw (g/mol)-Density (g/mL) Amount Compound Methyl cinnamate KOH MeOH Cinnamic acid product 162.19 56.11 32.04 1.09 2.12 0.79 N/A produet mL NA Experimental: 1. Set up a water bath and maintain at a temperature of roughly 35°C. 2. Combine the cinnamate, KOH, and methanol into the 25 ml round bottom flask. 3. Position the flask into the water bath so that the water of the bath rests...
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...
Organic chemistry post-lab question: "Why is important
to add the alkyl halide dropwise in your reaction? (Hint: your
reaction is not heated, but you still need a water-cooled
condenser!)" Please answer in detail!
Here is a copy of the experiment, thank you!
The Grignard reaction is an important synthetic process by which a carbon-carbon bond is formed. Magnesium metal is first reacted with an organic halide. The resultant organo-magnesium halide (Grignard reagent) is then combined with a carbonyl compound, ultimately...
Synthesis of dimedone This lab exercise will give you practical experience with the generation of a malonic ester enolate and subsequent reaction with an a,p-unsaturated carbonyl compound. This sequence is known as the Michael reaction. In the presence of sodium methoxide, dimethyl propanedioate (malonic ester/dimethyl malonate) is converted to the corresponding enolate anion and reaction with 4-methylpent-3-en-2-one (mesityl oxide) affords the Michael adduct 1, as shown in the reaction sequence below. Under the basic reaction conditions, the Michael adduct 1...
Synthesis of dimedone This lab exercise will give you practical experience with the generation of a malonic ester enolate and subsequent reaction with an a,p-unsaturated carbonyl compound. This sequence is known as the Michael reaction. In the presence of sodium methoxide, dimethyl propanedioate (malonic ester/dimethyl malonate) is converted to the corresponding enolate anion and reaction with 4-methylpent-3-en-2-one (mesityl oxide) affords the Michael adduct 1, as shown in the reaction sequence below. Under the basic reaction conditions, the Michael adduct 1...
Working on the questions at the end of this lab report
(see above). I need help answering questions 2, 3, and 4 completely
and thoroughly. Thank you!
s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...
It's a weak acid strong base titration
Experiment 4: Identification of an unknown acid by titration Page 2 of 15 Background In this experiment, you will use both qualitative and quantitative properties to determine an unknown acid's identity and concentration. To do this analysis, you will perform a titration of your unknown acid sample-specifically a potentiometric titration where you use a pH meter and record pH values during the titration, combined with a visual titration using a color indi- cator...
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